跳转至内容
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

登录 查看组织和合同定价。

选择尺寸

关于此项目

线性分子式:
HOC6H4CO2H
化学文摘社编号:
99-96-7
分子量:
138.12
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24854406
EC Number:
202-804-9
Beilstein/REAXYS Number:
970950
MDL number:
MFCD00002547

主要文件

查看所有文档
技术服务
需要帮助？我们经验丰富的科学家团队随时乐意为您服务。
让我们为您提供帮助
技术服务
需要帮助？我们经验丰富的科学家团队随时乐意为您服务。
让我们为您提供帮助

产品名称

对羟基苯甲酸, ReagentPlus®, ≥99%

InChI key

FJKROLUGYXJWQN-UHFFFAOYSA-N

InChI

1S/C7H6O3/c8-6-3-1-5(2-4-6)7(9)10/h1-4,8H,(H,9,10)

SMILES string

OC(=O)c1ccc(O)cc1

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

Quality Level

100

正在寻找类似产品? 访问 产品对比指南

相关类别

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。

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。

Legal Information

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

pictograms

CorrosionExclamation mark
GHS05,GHS07

signalword

Danger

hcodes

H318,H335

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
0000516856
0000516856
0000505436
0000505436
0000498591

没有发现合适的版本？

如果您需要特殊版本，可通过批号或批次号查找具体证书。

搜索COA

已有该产品？

在文件库中查找您最近购买产品的文档。

访问文档库

  1. Which document(s) contains shelf-life or expiration date information for a given product?

    If available for a given product, the recommended re-test date or the expiration date can be found on the Certificate of Analysis.

  2. How do I get lot-specific information or a Certificate of Analysis?

    The lot specific COA document can be found by entering the lot number above under the "Documents" section.

  3. How do I find price and availability?

    There are several ways to find pricing and availability for our products. Once you log onto our website, you will find the price and availability displayed on the product detail page. You can contact any of our Customer Sales and Service offices to receive a quote.  USA customers:  1-800-325-3010 or view local office numbers.

  4. How can Product 240141, 4-Hydroxybenzoic acid, be dissolved?

    According to the chemicals encyclopedia published by the Royal Society of Chemistry, 4-Hydroxybenzoic acid is freely soluble in alcohol, and soluble in about 125 parts water.

  5. What is the shelf life of Product 240141, 4-Hydroxybenzoic acid?

    This information can be found on the product specification sheet for a related product (H20059).

  6. I see that Product 240141, 4-Hydroxybenzoic acid, is deleted. Which product do you offer in its place?

    Our best offer item is Product No. H20059.

  7. What is the Department of Transportation shipping information for this product?

    Transportation information can be found in Section 14 of the product's (M)SDS.To access the shipping information for this material, use the link on the product detail page for the product. 

  8. My question is not addressed here, how can I contact Technical Service for assistance?

    Ask a Scientist here.

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
L C Goudas et al.
Anesthesia and analgesia, 89(5), 1209-1215 (1999-11-30)
Intracerebroventricular (ICV) morphine administration is effective for the management of refractory cancer pain. Recent preclinical observations of acute depletion of the major endogenous intracellular antioxidant glutathione (GSH) in brain and peripheral organs after ICV morphine in rodents led us to
Letian X Xie et al.
The Journal of biological chemistry, 287(28), 23571-23581 (2012-05-18)
Most of the Coq proteins involved in coenzyme Q (ubiquinone or Q) biosynthesis are interdependent within a multiprotein complex in the yeast Saccharomyces cerevisiae. Lack of only one Coq polypeptide, as in Δcoq strains, results in the degradation of several
查看所有相关文献

我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.

联系客户支持