{"id":3448,"date":"2024-07-12T06:47:26","date_gmt":"2024-07-12T06:47:26","guid":{"rendered":"https:\/\/pharm.sinocurechem.com\/?p=3448"},"modified":"2024-07-12T06:47:26","modified_gmt":"2024-07-12T06:47:26","slug":"4-hydroxybenzaldehyde-structure-synthesis-applications-and-safety","status":"publish","type":"post","link":"https:\/\/longchangextracts.com\/ru\/4-\u0433\u0438\u0434\u0440\u043e\u043a\u0441\u0438\u0431\u0435\u043d\u0437\u0430\u043b\u044c\u0434\u0435\u0433\u0438\u0434-\u0441\u0442\u0440\u0443\u043a\u0442\u0443\u0440\u0430-\u0441\u0438\u043d\/","title":{"rendered":"4-\u0433\u0438\u0434\u0440\u043e\u043a\u0441\u0438\u0431\u0435\u043d\u0437\u0430\u043b\u044c\u0434\u0435\u0433\u0438\u0434: \u0441\u0442\u0440\u0443\u043a\u0442\u0443\u0440\u0430, \u0441\u0438\u043d\u0442\u0435\u0437, \u043f\u0440\u0438\u043c\u0435\u043d\u0435\u043d\u0438\u0435 \u0438 \u0431\u0435\u0437\u043e\u043f\u0430\u0441\u043d\u043e\u0441\u0442\u044c"},"content":{"rendered":"<p class=\"MsoNormal\" style=\"text-align: left;\" align=\"center\"><span style=\"text-indent: 0pt; font-family: Georgia; font-weight: bold; font-size: 14pt;\">1. <\/span><b style=\"text-indent: 0pt;\"><span style=\"font-family: Georgia; font-size: 14pt;\">Chemical Structure and Properties<\/span><\/b><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">Molecular Structure<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">4-Hydroxybenzaldehyde, also known as p-hydroxybenzaldehyde, has a benzene ring with two functional groups:<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">A hydroxyl group (-OH) at the para position (carbon 4).<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">An aldehyde group (-CHO) at the para position relative to the hydroxyl group.<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">The structural formula can be represented as:<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">\u00a0\u00a0\u00a0\u00a0OH<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">\u00a0\u00a0\u00a0\u00a0\u00a0|<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">\u00a0\u00a0C6H4<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">\u00a0\u00a0\u00a0\u00a0\u00a0|<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">\u00a0\u00a0\u00a0CHO<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">This positioning gives 4-Hydroxybenzaldehyde its unique reactivity profile.<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">Physical Properties<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">Appearance: White to light yellow crystalline powder.<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">Molecular Formula: C7H6O2.<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">Molecular Weight: 122.12 g\/mol.<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">Melting Point: 115-118 \u00b0C. The melting point indicates the temperature at which the solid form of 4-Hydroxybenzaldehyde transitions to a liquid state.<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">Boiling Point: 191-192 \u00b0C. This is the temperature at which 4-Hydroxybenzaldehyde transitions from a liquid to a gaseous state.<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">Density: 1.226 g\/cm\u00b3. This property describes the mass per unit volume of 4-Hydroxybenzaldehyde.<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">Refractive Index: 1.579. This indicates how light propagates through the compound.<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">Solubility<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">Water Solubility: Slightly soluble. The hydroxyl group increases solubility in water compared to other benzaldehydes.<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">Organic Solvents: Soluble in ethanol, ether, and chloroform. This high solubility in organic solvents makes it versatile for use in organic synthesis.<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">Spectroscopic Properties<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">UV-Vis Spectroscopy: Shows characteristic absorption peaks due to the aromatic ring and conjugated system.<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">IR Spectroscopy:<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">Broad band around 3200-3600 cm\u207b\u00b9 due to O-H stretching vibrations.<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">Strong peak around 1680-1700 cm\u207b\u00b9 due to the C=O stretching vibration of the aldehyde group.<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">Peaks in the region of 1400-1600 cm\u207b\u00b9 corresponding to C=C stretching vibrations of the benzene ring.<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">NMR Spectroscopy:<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">Proton NMR (\u00b9H NMR): The aldehyde proton appears as a singlet around 9-10 ppm. The aromatic protons typically appear in the range of 6-8 ppm, with the hydroxyl proton appearing around 4-5 ppm.<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">Carbon-13 NMR (\u00b9\u00b3C NMR): The aldehyde carbon shows a peak around 190-200 ppm, and aromatic carbons appear in the range of 110-160 ppm.<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">Chemical Reactivity<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">Aldehyde Reactivity: The -CHO group can participate in nucleophilic addition reactions, oxidation to carboxylic acids, and reduction to alcohols.<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">Hydroxyl Reactivity: The -OH group can undergo typical phenolic reactions, including esterification, etherification, and electrophilic aromatic substitution.<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">Electrophilic Aromatic Substitution: The hydroxyl group activates the benzene ring towards electrophilic aromatic substitution, particularly at the ortho and para positions relative to the hydroxyl group.<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">Stability<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">4-Hydroxybenzaldehyde is relatively stable under normal conditions but should be stored in a cool, dry place away from strong oxidizing agents. Exposure to light and air can lead to gradual oxidation and degradation, affecting its purity and efficacy.<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">Derivatives<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">4-Hydroxybenzaldehyde can be chemically modified to produce various derivatives:<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">4-Hydroxybenzoic Acid: Through oxidation of the aldehyde group.<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">4-Methoxybenzaldehyde: By methylation of the hydroxyl group.<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">Schiff Bases: Formed by condensation with amines.<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">These derivatives expand the utility of 4-Hydroxybenzaldehyde in different applications, including pharmaceuticals, fragrances, and organic synthesis.<\/span><\/p>\n<p class=\"MsoNormal\" style=\"margin-left: 0.0000pt; mso-para-margin-left: 0.0000gd; text-indent: 0.0000pt; mso-char-indent-count: 0.0000; text-autospace: ideograph-numeric; mso-pagination: none; mso-list: l1 level1 lfo1;\"><!-- [if !supportLists]--><span style=\"font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-weight: bold; font-size: 14.0000pt; mso-font-kerning: 1.0000pt;\">2.\u00a0<\/span><!--[endif]--><b><span style=\"font-family: Georgia; font-size: 14pt;\">Synthesis of 4-Hydroxybenzaldehyde<\/span><\/b><b><\/b><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">4-Hydroxybenzaldehyde can be synthesized through several methods, each with its advantages depending on the required purity, yield, and specific application. Here are some common synthesis methods:<\/span><\/p>\n<p class=\"MsoNormal\" style=\"margin-left: 21.2500pt; mso-para-margin-left: 0.0000gd; text-indent: -21.2500pt; mso-char-indent-count: 0.0000; mso-list: l2 level1 lfo2;\"><!-- [if !supportLists]--><span style=\"font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-weight: bold; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">1)\u00a0<\/span><!--[endif]--><b><span style=\"font-family: Georgia; font-size: 12pt;\">Oxidation of 4-Hydroxytoluene (p-Cresol)<\/span><\/b><b><\/b><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">One of the most straightforward methods involves the oxidation of 4-hydroxytoluene:<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">Starting Material: p-Cresol (4-hydroxytoluene).<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">Oxidizing Agents: Common oxidizing agents include potassium permanganate (KMnO\u2084), chromium trioxide (CrO\u2083), or manganese dioxide (MnO\u2082).<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">Procedure:<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">Dissolve p-cresol in an appropriate solvent, such as water or a mixture of water and an organic solvent.<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">Add the oxidizing agent slowly while maintaining the reaction temperature.<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">Stir the reaction mixture until the oxidation is complete.<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">Filter the mixture to remove any precipitate and purify the product through recrystallization or distillation.<\/span><\/p>\n<p class=\"MsoNormal\" style=\"margin-left: 21.2500pt; mso-para-margin-left: 0.0000gd; text-indent: -21.2500pt; mso-char-indent-count: 0.0000; mso-list: l2 level1 lfo2;\"><!-- [if !supportLists]--><span style=\"font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-weight: bold; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">2)\u00a0<\/span><!--[endif]--><b><span style=\"font-family: Georgia; font-size: 12pt;\">Hydrolysis of 4-Hydroxybenzyl Alcohol<\/span><\/b><b><\/b><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">Hydrolysis of 4-hydroxybenzyl alcohol is another method to obtain 4-Hydroxybenzaldehyde:<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">Starting Material: 4-Hydroxybenzyl alcohol.<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">Reagents: Aqueous acid solution (such as hydrochloric acid, HCl) or catalytic amount of an acid.<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">Procedure:<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">Dissolve 4-hydroxybenzyl alcohol in an acid solution.<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">Heat the mixture under reflux.<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">After the reaction is complete, cool the mixture and extract the product.<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">Purify 4-Hydroxybenzaldehyde by recrystallization.<\/span><\/p>\n<p class=\"MsoNormal\" style=\"margin-left: 21.2500pt; mso-para-margin-left: 0.0000gd; text-indent: -21.2500pt; mso-char-indent-count: 0.0000; mso-list: l2 level1 lfo2;\"><!-- [if !supportLists]--><span style=\"font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-weight: bold; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">3)\u00a0<\/span><!--[endif]--><b><span style=\"font-family: Georgia; font-size: 12pt;\">Purification<\/span><\/b><b><\/b><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">After the synthesis, 4-Hydroxybenzaldehyde is typically purified to obtain the desired level of purity:<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">Recrystallization: Dissolve the crude product in a minimal amount of hot solvent (e.g., ethanol or water) and allow it to cool slowly. Crystals of pure 4-Hydroxybenzaldehyde will form.<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">Distillation: For purification through distillation, vacuum distillation can be used to avoid decomposition at high temperatures.<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">Chromatography: Column chromatography can be employed for further purification if required.<\/span><\/p>\n<p class=\"MsoNormal\" style=\"margin-left: 0.0000pt; mso-para-margin-left: 0.0000gd; text-indent: 0.0000pt; mso-char-indent-count: 0.0000; text-autospace: ideograph-numeric; mso-pagination: none; mso-list: l1 level1 lfo1;\"><!-- [if !supportLists]--><span style=\"font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-weight: bold; font-size: 14.0000pt; mso-font-kerning: 1.0000pt;\">3.\u00a0<\/span><!--[endif]--><b><span style=\"font-family: Georgia; font-size: 14pt;\">Applications of 4-Hydroxybenzaldehyde<\/span><\/b><b><\/b><\/p>\n<p class=\"MsoNormal\" style=\"margin-left: 21.2500pt; mso-para-margin-left: 0.0000gd; text-indent: -21.2500pt; mso-char-indent-count: 0.0000; mso-list: l0 level1 lfo3;\"><!-- [if !supportLists]--><span style=\"font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-weight: bold; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">1)\u00a0<\/span><!--[endif]--><b><span style=\"font-family: Georgia; font-size: 12pt;\">Pharmaceuticals<\/span><\/b><b><\/b><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">Intermediate in Drug Synthesis:<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">4-Hydroxybenzaldehyde serves as a key intermediate in the synthesis of several pharmaceutical compounds.<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">It is used in the production of antihypertensive agents, anti-inflammatory drugs, and antimicrobial compounds. For instance, it is a precursor in the synthesis of 4-Hydroxyphenylglycine, which is used in the manufacture of certain antibiotics.<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">Analytical Reagent:<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">It is employed as a derivatizing agent in analytical chemistry for the quantitative determination of various pharmaceutical substances.<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">Its ability to form Schiff bases with amines makes it useful in the detection and analysis of amino-containing drugs.<\/span><\/p>\n<p class=\"MsoNormal\" style=\"margin-left: 21.2500pt; mso-para-margin-left: 0.0000gd; text-indent: -21.2500pt; mso-char-indent-count: 0.0000; mso-list: l0 level1 lfo3;\"><!-- [if !supportLists]--><span style=\"font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-weight: bold; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">2)\u00a0<\/span><!--[endif]--><b><span style=\"font-family: Georgia; font-size: 12pt;\">2. Flavors and Fragrances<\/span><\/b><b><\/b><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">Aroma Compound:<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">4-Hydroxybenzaldehyde is utilized as a flavoring agent in the food industry due to its pleasant almond-like odor.<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">It is a component in the formulation of various fragrances used in perfumes, soaps, and cosmetics.<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">Synthesis of Vanillin:<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">It is an important intermediate in the synthesis of vanillin (4-Hydroxy-3-methoxybenzaldehyde), one of the most popular flavoring agents used in food products, beverages, and pharmaceuticals.<\/span><\/p>\n<p class=\"MsoNormal\" style=\"margin-left: 21.2500pt; mso-para-margin-left: 0.0000gd; text-indent: -21.2500pt; mso-char-indent-count: 0.0000; mso-list: l0 level1 lfo3;\"><!-- [if !supportLists]--><span style=\"font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-weight: bold; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">3)\u00a0<\/span><!--[endif]--><b><span style=\"font-family: Georgia; font-size: 12pt;\">Organic Synthesis<\/span><\/b><b><\/b><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">Building Block:<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">4-Hydroxybenzaldehyde is a valuable building block in organic synthesis, contributing to the construction of more complex molecules.<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">It is used in the synthesis of heterocyclic compounds, which have applications in pharmaceuticals and agrochemicals.<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">Cross-Coupling Reactions:<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">It participates in Suzuki and Heck coupling reactions, facilitating the formation of carbon-carbon bonds essential in the synthesis of biaryl compounds and other complex structures.<\/span><\/p>\n<p class=\"MsoNormal\" style=\"margin-left: 21.2500pt; mso-para-margin-left: 0.0000gd; text-indent: -21.2500pt; mso-char-indent-count: 0.0000; mso-list: l0 level1 lfo3;\"><!-- [if !supportLists]--><span style=\"font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-weight: bold; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">4)\u00a0<\/span><!--[endif]--><b><span style=\"font-family: Georgia; font-size: 12pt;\">Biological Research<\/span><\/b><b><\/b><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">Enzyme Inhibition Studies:<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">4-Hydroxybenzaldehyde is used in biochemical research to study the inhibition of specific enzymes.<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">It helps in understanding enzyme function and regulation, which is crucial for drug development and therapeutic interventions.<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">Antioxidant Research:<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">It is investigated for its antioxidant properties, contributing to studies on oxidative stress and related diseases.<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">Its ability to scavenge free radicals makes it a candidate for research in the prevention and treatment of conditions associated with oxidative damage.<\/span><\/p>\n<p class=\"MsoNormal\" style=\"margin-left: 21.2500pt; mso-para-margin-left: 0.0000gd; text-indent: -21.2500pt; mso-char-indent-count: 0.0000; mso-list: l0 level1 lfo3;\"><!-- [if !supportLists]--><span style=\"font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-weight: bold; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">5)\u00a0<\/span><!--[endif]--><b><span style=\"font-family: Georgia; font-size: 12pt;\">Polymer Industry<\/span><\/b><b><\/b><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">Polymer Additive:<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">It is used as a precursor in the synthesis of phenolic resins and other polymeric materials.<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">These polymers are employed in coatings, adhesives, and composite materials, offering enhanced mechanical and thermal properties.<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">Stabilizers:<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">4-Hydroxybenzaldehyde can act as a stabilizer in the polymerization processes, improving the stability and performance of the final polymer products.<\/span><\/p>\n<p class=\"MsoNormal\" style=\"margin-left: 21.2500pt; mso-para-margin-left: 0.0000gd; text-indent: -21.2500pt; mso-char-indent-count: 0.0000; mso-list: l0 level1 lfo3;\"><!-- [if !supportLists]--><span style=\"font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-weight: bold; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">6)\u00a0<\/span><!--[endif]--><b><span style=\"font-family: Georgia; font-size: 12pt;\">Agrochemicals<\/span><\/b><b><\/b><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">Pesticides and Herbicides:<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">It is a precursor in the synthesis of various agrochemicals, including pesticides and herbicides.<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">These compounds are crucial for pest control and improving agricultural productivity.<\/span><\/p>\n<p class=\"MsoNormal\" style=\"margin-left: 21.2500pt; mso-para-margin-left: 0.0000gd; text-indent: -21.2500pt; mso-char-indent-count: 0.0000; mso-list: l0 level1 lfo3;\"><!-- [if !supportLists]--><span style=\"font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-weight: bold; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">7)\u00a0<\/span><!--[endif]--><b><span style=\"font-family: Georgia; font-size: 12pt;\">Dyes and Pigments<\/span><\/b><b><\/b><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">Synthesis of Dyes:<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">It is used in the production of azo dyes and other colorants.<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">These dyes find applications in textiles, inks, and coatings, providing vibrant and durable colors.<\/span><\/p>\n<p class=\"MsoNormal\" style=\"margin-left: 0.0000pt; mso-para-margin-left: 0.0000gd; text-indent: 0.0000pt; mso-char-indent-count: 0.0000; text-autospace: ideograph-numeric; mso-pagination: none; mso-list: l1 level1 lfo1;\"><!-- [if !supportLists]--><span style=\"font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-weight: bold; font-size: 14.0000pt; mso-font-kerning: 1.0000pt;\">4.\u00a0<\/span><!--[endif]--><b><span style=\"font-family: Georgia; font-size: 14pt;\">Safety and Handling<\/span><\/b><b><\/b><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">May cause skin and eye irritation; harmful if swallowed or inhaled.<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">Use gloves, safety goggles, and lab coats to prevent contact.<\/span><\/p>\n<p class=\"MsoNormal\"><span style=\"mso-spacerun: 'yes'; font-family: Georgia; mso-fareast-font-family: \u5b8b\u4f53; font-size: 12.0000pt; mso-font-kerning: 1.0000pt;\">Store in a cool, dry place away from incompatible substances such as strong oxidizers.<\/span><\/p>\n","protected":false},"excerpt":{"rendered":"<p>1. Chemical Structure and Properties Molecular Structure 4-Hydroxybenzaldehyde, also known as p-hydroxybenzaldehyde, has a benzene ring with two functional groups: A hydroxyl group (-OH) at the para position (carbon 4). An aldehyde group (-CHO) at the para position relative to the hydroxyl group. The structural formula can be represented as: \u00a0\u00a0\u00a0\u00a0OH \u00a0\u00a0\u00a0\u00a0\u00a0| \u00a0\u00a0C6H4 \u00a0\u00a0\u00a0\u00a0\u00a0| \u00a0\u00a0\u00a0CHO [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[20],"tags":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v23.0 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>4-Hydroxybenzaldehyde: Structure, Synthesis, Applications, and Safety - China Chemical Manufacturer<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/longchangextracts.com\/ru\/4-\u0433\u0438\u0434\u0440\u043e\u043a\u0441\u0438\u0431\u0435\u043d\u0437\u0430\u043b\u044c\u0434\u0435\u0433\u0438\u0434-\u0441\u0442\u0440\u0443\u043a\u0442\u0443\u0440\u0430-\u0441\u0438\u043d\/\" \/>\n<meta property=\"og:locale\" content=\"ru_RU\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"4-Hydroxybenzaldehyde: Structure, Synthesis, Applications, and Safety - China Chemical Manufacturer\" \/>\n<meta property=\"og:description\" content=\"1. Chemical Structure and Properties Molecular Structure 4-Hydroxybenzaldehyde, also known as p-hydroxybenzaldehyde, has a benzene ring with two functional groups: A hydroxyl group (-OH) at the para position (carbon 4). An aldehyde group (-CHO) at the para position relative to the hydroxyl group. The structural formula can be represented as: \u00a0\u00a0\u00a0\u00a0OH \u00a0\u00a0\u00a0\u00a0\u00a0| \u00a0\u00a0C6H4 \u00a0\u00a0\u00a0\u00a0\u00a0| \u00a0\u00a0\u00a0CHO [&hellip;]\" \/>\n<meta property=\"og:url\" content=\"https:\/\/longchangextracts.com\/ru\/4-\u0433\u0438\u0434\u0440\u043e\u043a\u0441\u0438\u0431\u0435\u043d\u0437\u0430\u043b\u044c\u0434\u0435\u0433\u0438\u0434-\u0441\u0442\u0440\u0443\u043a\u0442\u0443\u0440\u0430-\u0441\u0438\u043d\/\" \/>\n<meta property=\"og:site_name\" content=\"China Chemical Manufacturer\" \/>\n<meta property=\"article:published_time\" content=\"2024-07-12T06:47:26+00:00\" \/>\n<meta name=\"author\" content=\"longcha9\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:label1\" content=\"\u041d\u0430\u043f\u0438\u0441\u0430\u043d\u043e \u0430\u0432\u0442\u043e\u0440\u043e\u043c\" \/>\n\t<meta name=\"twitter:data1\" content=\"longcha9\" \/>\n\t<meta name=\"twitter:label2\" content=\"\u041f\u0440\u0438\u043c\u0435\u0440\u043d\u043e\u0435 \u0432\u0440\u0435\u043c\u044f \u0434\u043b\u044f \u0447\u0442\u0435\u043d\u0438\u044f\" \/>\n\t<meta name=\"twitter:data2\" content=\"6 \u043c\u0438\u043d\u0443\u0442\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\/\/schema.org\",\"@graph\":[{\"@type\":\"WebPage\",\"@id\":\"https:\/\/longchangextracts.com\/4-hydroxybenzaldehyde-structure-synthesis-applications-and-safety\/\",\"url\":\"https:\/\/longchangextracts.com\/4-hydroxybenzaldehyde-structure-synthesis-applications-and-safety\/\",\"name\":\"4-Hydroxybenzaldehyde: Structure, Synthesis, Applications, and Safety - China Chemical Manufacturer\",\"isPartOf\":{\"@id\":\"https:\/\/longchangextracts.com\/#website\"},\"datePublished\":\"2024-07-12T06:47:26+00:00\",\"dateModified\":\"2024-07-12T06:47:26+00:00\",\"author\":{\"@id\":\"https:\/\/longchangextracts.com\/#\/schema\/person\/80933ac6926ad63fea74ec33f8d04869\"},\"breadcrumb\":{\"@id\":\"https:\/\/longchangextracts.com\/4-hydroxybenzaldehyde-structure-synthesis-applications-and-safety\/#breadcrumb\"},\"inLanguage\":\"ru-RU\",\"potentialAction\":[{\"@type\":\"ReadAction\",\"target\":[\"https:\/\/longchangextracts.com\/4-hydroxybenzaldehyde-structure-synthesis-applications-and-safety\/\"]}]},{\"@type\":\"BreadcrumbList\",\"@id\":\"https:\/\/longchangextracts.com\/4-hydroxybenzaldehyde-structure-synthesis-applications-and-safety\/#breadcrumb\",\"itemListElement\":[{\"@type\":\"ListItem\",\"position\":1,\"name\":\"Home\",\"item\":\"https:\/\/longchangextracts.com\/\"},{\"@type\":\"ListItem\",\"position\":2,\"name\":\"4-Hydroxybenzaldehyde: Structure, Synthesis, Applications, and Safety\"}]},{\"@type\":\"WebSite\",\"@id\":\"https:\/\/longchangextracts.com\/#website\",\"url\":\"https:\/\/longchangextracts.com\/\",\"name\":\"China Chemical Manufacturer\",\"description\":\"\",\"potentialAction\":[{\"@type\":\"SearchAction\",\"target\":{\"@type\":\"EntryPoint\",\"urlTemplate\":\"https:\/\/longchangextracts.com\/?s={search_term_string}\"},\"query-input\":\"required name=search_term_string\"}],\"inLanguage\":\"ru-RU\"},{\"@type\":\"Person\",\"@id\":\"https:\/\/longchangextracts.com\/#\/schema\/person\/80933ac6926ad63fea74ec33f8d04869\",\"name\":\"longcha9\",\"image\":{\"@type\":\"ImageObject\",\"inLanguage\":\"ru-RU\",\"@id\":\"https:\/\/longchangextracts.com\/#\/schema\/person\/image\/\",\"url\":\"https:\/\/secure.gravatar.com\/avatar\/c1e84ee0759373263198c58e8f338f80?s=96&d=mm&r=g\",\"contentUrl\":\"https:\/\/secure.gravatar.com\/avatar\/c1e84ee0759373263198c58e8f338f80?s=96&d=mm&r=g\",\"caption\":\"longcha9\"}}]}<\/script>\n<!-- \/ Yoast SEO plugin. -->","yoast_head_json":{"title":"4-\u0433\u0438\u0434\u0440\u043e\u043a\u0441\u0438\u0431\u0435\u043d\u0437\u0430\u043b\u044c\u0434\u0435\u0433\u0438\u0434: \u0441\u0442\u0440\u0443\u043a\u0442\u0443\u0440\u0430, \u0441\u0438\u043d\u0442\u0435\u0437, \u043f\u0440\u0438\u043c\u0435\u043d\u0435\u043d\u0438\u0435 \u0438 \u0431\u0435\u0437\u043e\u043f\u0430\u0441\u043d\u043e\u0441\u0442\u044c - \u041a\u0438\u0442\u0430\u0439\u0441\u043a\u0438\u0439 \u0445\u0438\u043c\u0438\u0447\u0435\u0441\u043a\u0438\u0439 \u043f\u0440\u043e\u0438\u0437\u0432\u043e\u0434\u0438\u0442\u0435\u043b\u044c","robots":{"index":"index","follow":"follow","max-snippet":"max-snippet:-1","max-image-preview":"max-image-preview:large","max-video-preview":"max-video-preview:-1"},"canonical":"https:\/\/longchangextracts.com\/ru\/4-\u0433\u0438\u0434\u0440\u043e\u043a\u0441\u0438\u0431\u0435\u043d\u0437\u0430\u043b\u044c\u0434\u0435\u0433\u0438\u0434-\u0441\u0442\u0440\u0443\u043a\u0442\u0443\u0440\u0430-\u0441\u0438\u043d\/","og_locale":"ru_RU","og_type":"article","og_title":"4-Hydroxybenzaldehyde: Structure, Synthesis, Applications, and Safety - China Chemical Manufacturer","og_description":"1. Chemical Structure and Properties Molecular Structure 4-Hydroxybenzaldehyde, also known as p-hydroxybenzaldehyde, has a benzene ring with two functional groups: A hydroxyl group (-OH) at the para position (carbon 4). An aldehyde group (-CHO) at the para position relative to the hydroxyl group. The structural formula can be represented as: \u00a0\u00a0\u00a0\u00a0OH \u00a0\u00a0\u00a0\u00a0\u00a0| \u00a0\u00a0C6H4 \u00a0\u00a0\u00a0\u00a0\u00a0| \u00a0\u00a0\u00a0CHO [&hellip;]","og_url":"https:\/\/longchangextracts.com\/ru\/4-\u0433\u0438\u0434\u0440\u043e\u043a\u0441\u0438\u0431\u0435\u043d\u0437\u0430\u043b\u044c\u0434\u0435\u0433\u0438\u0434-\u0441\u0442\u0440\u0443\u043a\u0442\u0443\u0440\u0430-\u0441\u0438\u043d\/","og_site_name":"China Chemical Manufacturer","article_published_time":"2024-07-12T06:47:26+00:00","author":"longcha9","twitter_card":"summary_large_image","twitter_misc":{"\u041d\u0430\u043f\u0438\u0441\u0430\u043d\u043e \u0430\u0432\u0442\u043e\u0440\u043e\u043c":"longcha9","\u041f\u0440\u0438\u043c\u0435\u0440\u043d\u043e\u0435 \u0432\u0440\u0435\u043c\u044f \u0434\u043b\u044f \u0447\u0442\u0435\u043d\u0438\u044f":"6 \u043c\u0438\u043d\u0443\u0442"},"schema":{"@context":"https:\/\/schema.org","@graph":[{"@type":"WebPage","@id":"https:\/\/longchangextracts.com\/4-hydroxybenzaldehyde-structure-synthesis-applications-and-safety\/","url":"https:\/\/longchangextracts.com\/4-hydroxybenzaldehyde-structure-synthesis-applications-and-safety\/","name":"4-\u0433\u0438\u0434\u0440\u043e\u043a\u0441\u0438\u0431\u0435\u043d\u0437\u0430\u043b\u044c\u0434\u0435\u0433\u0438\u0434: \u0441\u0442\u0440\u0443\u043a\u0442\u0443\u0440\u0430, \u0441\u0438\u043d\u0442\u0435\u0437, \u043f\u0440\u0438\u043c\u0435\u043d\u0435\u043d\u0438\u0435 \u0438 \u0431\u0435\u0437\u043e\u043f\u0430\u0441\u043d\u043e\u0441\u0442\u044c - \u041a\u0438\u0442\u0430\u0439\u0441\u043a\u0438\u0439 \u0445\u0438\u043c\u0438\u0447\u0435\u0441\u043a\u0438\u0439 \u043f\u0440\u043e\u0438\u0437\u0432\u043e\u0434\u0438\u0442\u0435\u043b\u044c","isPartOf":{"@id":"https:\/\/longchangextracts.com\/#website"},"datePublished":"2024-07-12T06:47:26+00:00","dateModified":"2024-07-12T06:47:26+00:00","author":{"@id":"https:\/\/longchangextracts.com\/#\/schema\/person\/80933ac6926ad63fea74ec33f8d04869"},"breadcrumb":{"@id":"https:\/\/longchangextracts.com\/4-hydroxybenzaldehyde-structure-synthesis-applications-and-safety\/#breadcrumb"},"inLanguage":"ru-RU","potentialAction":[{"@type":"ReadAction","target":["https:\/\/longchangextracts.com\/4-hydroxybenzaldehyde-structure-synthesis-applications-and-safety\/"]}]},{"@type":"BreadcrumbList","@id":"https:\/\/longchangextracts.com\/4-hydroxybenzaldehyde-structure-synthesis-applications-and-safety\/#breadcrumb","itemListElement":[{"@type":"ListItem","position":1,"name":"Home","item":"https:\/\/longchangextracts.com\/"},{"@type":"ListItem","position":2,"name":"4-Hydroxybenzaldehyde: Structure, Synthesis, Applications, and Safety"}]},{"@type":"WebSite","@id":"https:\/\/longchangextracts.com\/#website","url":"https:\/\/longchangextracts.com\/","name":"\u041a\u0438\u0442\u0430\u0439\u0441\u043a\u0438\u0439 \u0445\u0438\u043c\u0438\u0447\u0435\u0441\u043a\u0438\u0439 \u043f\u0440\u043e\u0438\u0437\u0432\u043e\u0434\u0438\u0442\u0435\u043b\u044c","description":"","potentialAction":[{"@type":"SearchAction","target":{"@type":"EntryPoint","urlTemplate":"https:\/\/longchangextracts.com\/?s={search_term_string}"},"query-input":"required name=search_term_string"}],"inLanguage":"ru-RU"},{"@type":"Person","@id":"https:\/\/longchangextracts.com\/#\/schema\/person\/80933ac6926ad63fea74ec33f8d04869","name":"\u043b\u043e\u043d\u0447\u04309","image":{"@type":"ImageObject","inLanguage":"ru-RU","@id":"https:\/\/longchangextracts.com\/#\/schema\/person\/image\/","url":"https:\/\/secure.gravatar.com\/avatar\/c1e84ee0759373263198c58e8f338f80?s=96&d=mm&r=g","contentUrl":"https:\/\/secure.gravatar.com\/avatar\/c1e84ee0759373263198c58e8f338f80?s=96&d=mm&r=g","caption":"longcha9"}}]}},"_links":{"self":[{"href":"https:\/\/longchangextracts.com\/ru\/wp-json\/wp\/v2\/posts\/3448"}],"collection":[{"href":"https:\/\/longchangextracts.com\/ru\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/longchangextracts.com\/ru\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/longchangextracts.com\/ru\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/longchangextracts.com\/ru\/wp-json\/wp\/v2\/comments?post=3448"}],"version-history":[{"count":0,"href":"https:\/\/longchangextracts.com\/ru\/wp-json\/wp\/v2\/posts\/3448\/revisions"}],"wp:attachment":[{"href":"https:\/\/longchangextracts.com\/ru\/wp-json\/wp\/v2\/media?parent=3448"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/longchangextracts.com\/ru\/wp-json\/wp\/v2\/categories?post=3448"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/longchangextracts.com\/ru\/wp-json\/wp\/v2\/tags?post=3448"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}