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Merck
CN

240141

对羟基苯甲酸

ReagentPlus®, ≥99%

别名:

4-苯酚甲酸, 对水杨酸, 对羟基苯甲酸, 对苯酚甲酸

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关于此项目

线性分子式:
HOC6H4CO2H
化学文摘社编号:
分子量:
138.12
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-804-9
Beilstein/REAXYS Number:
970950
MDL number:
Assay:
≥99%
Form:
powder
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Quality Level

product line

ReagentPlus®

assay

≥99%

form

powder

mp

213-217 °C (lit.)

solubility

water: soluble 125 part(lit.), acetone: soluble(lit.), alcohol: freely soluble(lit.), carbon disulfide: insoluble(lit.), chloroform: slightly soluble(lit.), diethyl ether: soluble(lit.)

functional group

carboxylic acid

SMILES string

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

General description

4-羟基苯甲酸是一种芳香羧酸,常用作各种有机反应的合成砌块,如可用于合成液晶和对羟基苯甲酸酯。还用于酯化反应合成芳香低聚物。

Application

4-羟基苯甲酸可用作合成以下物质的反应物:
  • 通过与蔗糖的酯化反应合成的单酯。
  • 热致液晶聚合物。.
  • 通过一锅化学酶法合成的2-羟基苯甲醛肟

Legal Information

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany


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pictograms

CorrosionExclamation mark

signalword

Danger

hcodes

Hazard Classifications

Eye Dam. 1 - STOT SE 3

target_organs

Respiratory system

存储类别

11 - Combustible Solids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves



历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Meng Wang et al.
ACS catalysis, 4(4), 1219-1225 (2014-05-08)
The adenylation (A) domain acts as the first "gate-keeper" to ensure the activation and thioesterification of the correct monomer to nonribosomal peptide synthetases (NRPSs). Our understanding of the specificity-conferring code and our ability to engineer A domains are critical for
Thermotropic liquid crystalline polymers as protective coatings for aerospace
Guerriero G, et al.
Progress in Organic Coatings, 70, 245-251 (2011)
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



全球贸易项目编号

货号GTIN
240141-50G04061838787682