主要文件

查看所有文档

A7205

3-乙酰胺基苯酚

Name: 3-乙酰胺基苯酚
Brand: ALDRICH

97%

别名:

3′-羟基乙酰苯胺

登录查看组织和合同定价。

选择尺寸

变更视图

关于此项目

线性分子式:

CH₃CONHC₆H₄OH

化学文摘社编号:

621-42-1

分子量:

151.16

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24891188

EC Number:

210-687-0

Beilstein/REAXYS Number:

907998

MDL number:

MFCD00002263

Assay:

97%

Form:

crystals

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

属性

Quality Level

200

assay

97%

form

crystals

mp

145-148 °C (lit.)

SMILES string

CC(=O)Nc1cccc(O)c1

InChI

1S/C8H9NO2/c1-6(10)9-7-3-2-4-8(11)5-7/h2-5,11H,1H3,(H,9,10)

InChI key

QLNWXBAGRTUKKI-UHFFFAOYSA-N

说明

Still not finding the right product?

Explore all of our products under 3-乙酰胺基苯酚

pictograms

GHS07

signalword

Warning

hcodes

H315,H319

pcodes

P264 - P280 - P302 + P352 - P305 + P351 + P338 - P332 + P313 - P337 + P313

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2

存储类别

11 - Combustible Solids

wgk

WGK 2

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

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

The microsomal metabolism and site of covalent binding to protein of 3'-hydroxyacetanilide, a nonhepatotoxic positional isomer of acetaminophen.

A J Streeter et al.

Drug metabolism and disposition: the biological fate of chemicals, 12(5), 565-576 (1984-09-01)

Incubations of 3'-hydroxyacetanilide (3HAA) with hepatic microsomal preparations from phenobarbital-pretreated mice led to the formation of three products of aromatic hydroxylation, viz. 2',5'-, 3',4'-, and 2',3'-dihydroxyacetanilide, which were identified by GC/MS techniques and quantified by GLC analysis. NADPH-dependent covalent binding

Characterization of glutathione conjugates of reactive metabolites of 3'-hydroxyacetanilide, a nonhepatotoxic positional isomer of acetaminophen.

M S Rashed et al.

Chemical research in toxicology, 2(1), 41-45 (1989-01-01)

3'-Hydroxyacetanilide (AMAP) is a nonhepatotoxic regioisomer of acetaminophen (APAP) that nonetheless does form reactive metabolites which bind to hepatic proteins. Because differences in the nature of reactive metabolites formed from AMAP and APAP may explain differences in their propensity to

A comparative study of mouse liver proteins arylated by reactive metabolites of acetaminophen and its nonhepatotoxic regioisomer, 3'-hydroxyacetanilide.

T G Myers et al.

Chemical research in toxicology, 8(3), 403-413 (1995-04-01)

Acetaminophen (4'-hydroxyacetanilide), a widely used analgesic/antipyretic drug, is hepatotoxic in large doses, whereas the m-hydroxy isomer of acetaminophen, 3'-hydroxyacetanilide, is not hepatotoxic. Both are oxidized by mouse liver cytochromes P-450 to reactive metabolites that bind covalently to hepatic proteins. Because

查看所有相关文献

全球贸易项目编号

货号	GTIN
A7205-100G	04061833383797
A7205-25G	04061832281452