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文件

安全信息

Y0000012

羟甲香豆素杂质A

European Pharmacopoeia (EP) Reference Standard

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别名:
Resorcinol, 1,3-苯二酚
线性分子式:
C6H4-1,3-(OH)2
CAS号:
108-46-3
分子量:
110.11
Beilstein:
906905
MDL编号:
MFCD00002269
PubChem化学物质编号:
329830814
NACRES:
NA.24

等级

pharmaceutical primary standard

蒸汽密度

3.8 (vs air)

蒸汽压

1 mmHg ( 21.1 °C)

API类

hymecromone

自燃温度

1126 °F

制造商/商品名称

EDQM

bp

178 °C/16 mmHg (lit.)

mp

109-112 °C (lit.)

应用

pharmaceutical (small molecule)

格式

neat

储存温度

2-8°C

SMILES字符串

Oc1cccc(O)c1

InChI

1S/C6H6O2/c7-5-2-1-3-6(8)4-5/h1-4,7-8H

InChI key

GHMLBKRAJCXXBS-UHFFFAOYSA-N

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相关类别

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

Hymecromone impurity A 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

危险分类

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 3 - Eye Dam. 1 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 1 Oral - STOT SE 2 Oral

靶器官

Respiratory system

储存分类代码

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

WGK

WGK 2

闪点(°F)

260.6 °F - closed cup

闪点(°C)

127 °C - closed cup

法规信息

危险化学品

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Frank Welsch
International journal of toxicology, 27(1), 59-63 (2008-02-23)
Medical case reports published in the 20th century over the course of several decades show that resorcinol caused reversible adverse effects on the human thyroid gland (TG) manifested as hypothyroidism. Affected patients had ulcerating leg varicosities and underwent prolonged treatment
Resorcinol.
IARC monographs on the evaluation of carcinogenic risks to humans, 71 Pt 3, 1119-1131 (1999-09-07)
Barry S Lynch et al.
Regulatory toxicology and pharmacology : RTP, 36(2), 198-210 (2002-12-04)
Resorcinol administered at high doses to rodents can disrupt thyroid hormone synthesis and can produce goitrogenic effects. These effects were not seen in a 2-year bioassay at doses of up to 520 mg/kg/day. There are species-specific differences in synthesis, binding
Ahmed M Elkhatat et al.
Advanced materials (Deerfield Beach, Fla.), 23(26), 2887-2903 (2011-05-25)
An overview on the preparation and properties of resorcinol-formaldehyde (RF) organic and carbon gels reveals the fascinating and remarkably flexible properties of RF carbon and organic gels and how these properties are related to the synthesis and processing conditions. The
Satoshi Yamaori et al.
Chemico-biological interactions, 215, 62-68 (2014-03-29)
We previously demonstrated that cannabidiol (CBD) was a potent mechanism-based inhibitor of human cytochrome P450 1A1 (CYP1A1). However, the moiety of CBD that contributes to the potent mechanism-based inhibition of human CYP1A1 remains unknown. Thus, the effects of compounds structurally
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