推荐产品
质量水平
产品线
ReagentPlus®
方案
99%
mp
213-217 °C (lit.)
溶解性
alcohol: freely soluble
SMILES字符串
OC(=O)c1ccc(O)cc1
InChI
1S/C7H6O3/c8-6-3-1-5(2-4-6)7(9)10/h1-4,8H,(H,9,10)
InChI key
FJKROLUGYXJWQN-UHFFFAOYSA-N
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一般描述
4-羟基苯甲酸(PHBA) 是苯甲酸的酚类衍生物，可用作合成聚合物的合成砌块。
应用
4-羟基苯甲酸可作为起始原料合成 4-乙酰氧基苯甲酸 和 4-羟基-3,5-二碘苯甲酸等有机中间体。
法律信息
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
警示用语：
Danger
危险声明
危险分类
Eye Dam. 1 - STOT SE 3
靶器官
Respiratory system
储存分类代码
11 - Combustible Solids
WGK
WGK 1
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
Formation of novel polymeric films derived from 4-hydroxybenzoic acid
Ferreira L, et al.
Materials Chemistry and Physics, 129, 46-52 (2011)
Esterification of Carboxylic Acids with Trialkyloxonium Salts: Ethyl and Methyl 4?Acetoxybenzoates: Benzoic acid, 4?(acetyloxy)?, ethyl and methyl esters.
Douglas J, et al.
Organic Syntheses, 56, 59-59 (1977)
2?Hydroxy?3, 5?diiodobenzoic Acid.
Woollett G H and Johnson W W
Organic Syntheses, 14, 52-52 (1943)
Behrooz Darbani
International journal of molecular sciences, 22(11) (2021-06-03)
Gene clusters are becoming promising tools for gene identification. The study reveals the purposive genomic distribution of genes toward higher inheritance rates of intact metabolic pathways/phenotypes and, thereby, higher fitness. The co-localization of co-expressed, co-interacting, and functionally related genes was
L I Wiebe et al.
Drug metabolism and disposition: the biological fate of chemicals, 6(3), 296-302 (1978-05-01)
Butylated hydroxytoluene (BHT) containing the stable isotope 13C was synthesized from 2-[13C]methylpropan-2-ol. A minor constituent of urine following ingestion of BHT-13C by a human volunteer was identified as 3,5-di-(1-[13C]methyl-1-methylethyl)-4-hydroxybenzoic acid, The major metabolite detected was 13C-labeled 5-carboxy-7-(1-carboxy-1-methylethyl)-3,3-dimethyl-2-hydroxy-2,3-dihydrobenzofuran. Detailed spectral analysis
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