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文件

Y0001470

苯甲酸

Name: 苯甲酸
Brand: SIAL

European Pharmacopoeia (EP) Reference Standard

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线性分子式:

C₆H₅COOH

CAS号:

65-85-0

分子量:

122.12

Beilstein:

636131

MDL编号:

MFCD00002398

PubChem化学物质编号:

329831440

NACRES:

NA.24

等级

pharmaceutical primary standard

Agency

Ph. Eur.

蒸汽密度

4.21 (vs air)

蒸汽压

10 mmHg ( 132 °C)

描述

API family: benfluorex

API类

mefenamic acid, benfluorex, metronidazole

自燃温度

1061 °F

制造商/商品名称

EDQM

存货情况

not available in (Sales restrictions may apply)

bp

249 °C (lit.)

mp

121-125 °C (lit.)

应用

pharmaceutical (small molecule)

格式

neat

储存温度

2-8°C

SMILES字符串

OC(=O)c1ccccc1

InChI

1S/C7H6O2/c8-7(9)6-4-2-1-3-5-6/h1-5H,(H,8,9)

InChI key

WPYMKLBDIGXBTP-UHFFFAOYSA-N

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一般描述

This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including SDS and any product information leaflets have been developed and issued under the Authority of the issuing Pharmacopoeia.For further information and support please go to the website of the issuing Pharmacopoeia.

应用

Benzoic acid EP Reference standard, intended for use in laboratory tests only as specifically prescribed in the European Pharmacopoeia.

包装

The product is delivered as supplied by the issuing Pharmacopoeia. For the current unit quantity, please visit the EDQM reference substance catalogue.

其他说明

Sales restrictions may apply.

警示用语：

Danger

危险声明

H315 - H318 - H372

预防措施声明

P280 - P302 + P352 - P305 + P351 + P338 + P310 - P314

危险分类

Eye Dam. 1 - Skin Irrit. 2 - STOT RE 1 Inhalation

靶器官

Lungs

储存分类代码

6.1C - Combustible, acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 1

分析证书(COA)

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示例

T1503

货号

25G

包装规格/数量

其它示例：

705578-5MG-PW

PL860-CGA/SHF-1EA

MMYOMAG-74K-13

1000309185

输入内容 1.000309185)

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Biosynthesis of biphenyls and benzophenones--evolution of benzoic acid-specific type III polyketide synthases in plants.

Ludger Beerhues et al.

Phytochemistry, 70(15-16), 1719-1727 (2009-08-25)

Type III polyketide synthases (PKSs) generate a diverse array of secondary metabolites by varying the starter substrate, the number of condensation reactions, and the mechanism of ring closure. Among the starter substrates used, benzoyl-CoA is a rare starter molecule. Biphenyl

Identification of a gene signature of a pre-transformation process by senescence evasion in normal human epidermal keratinocytes.

Nathalie Martin et al.

Molecular cancer, 13, 151-151 (2014-06-16)

Epidemiological data show that the incidence of carcinomas in humans is highly dependent on age. However, the initial steps of the age-related molecular oncogenic processes by which the switch towards the neoplastic state occurs remain poorly understood, mostly due to

Distinct nucleic acid interaction properties of HIV-1 nucleocapsid protein precursor NCp15 explain reduced viral infectivity.

Wei Wang et al.

Nucleic acids research, 42(11), 7145-7159 (2014-05-13)

During human immunodeficiency virus type 1 (HIV-1) maturation, three different forms of nucleocapsid (NC) protein-NCp15 (p9 + p6), NCp9 (p7 + SP2) and NCp7-appear successively. A mutant virus expressing NCp15 shows greatly reduced infectivity. Mature NCp7 is a chaperone protein

The biochemistry and toxicology of benzoic acid metabolism and its relationship to the elimination of waste nitrogen.

G C Tremblay et al.

Pharmacology & therapeutics, 60(1), 63-90 (1993-10-01)

Detoxification of sodium benzoate by elimination as a conjugate with glycine, a nonessential amino acid, provides a pathway for the disposal of waste nitrogen. Since 1979, sodium benzoate has been widely used in the therapeutic regimen to combat ammonia toxicity

The bacterial degradation of benzoic acid and benzenoid compounds under anaerobic conditions: unifying trends and new perspectives.

D J Elder et al.

FEMS microbiology reviews, 13(4), 441-468 (1994-04-01)

Simple homocyclic aromatic compounds are extremely abundant in the environment and are derived largely from lignin. Such compounds may enter anaerobic environments and several groups of bacteria, exhibiting diverse energy-yielding mechanisms, have evolved the capacity to overcome the thermodynamic stability

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