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Merck
CN

13-2291

Sigma-Aldrich

羟胺 盐酸盐

≥97.0%, suitable for determination of toxic metals

别名:

盐酸羟胺

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About This Item

线性分子式:
NH2OH · HCl
CAS号:
分子量:
69.49
Beilstein:
3539763
EC 号:
MDL编号:
UNSPSC代码:
12352301
PubChem化学物质编号:
方案:
≥97.0%
表单:
crystalline
溶解性:
water: soluble

方案

≥97.0%

表单

crystalline

存货情况

available only in Japan

技术

inhibition assay: suitable

pH值(酸碱度)

2.5-3.5 (20 °C, 50 g/L)

mp

155-157 °C (dec.) (lit.)

溶解性

water: soluble

密度

1.67 g/mL at 25 °C (lit.)

适用性

suitable for determination of toxic metals

SMILES字符串

Cl.NO

InChI

1S/ClH.H3NO/c;1-2/h1H;2H,1H2

InChI key

WTDHULULXKLSOZ-UHFFFAOYSA-N

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生化/生理作用

MAO 抑制剂;抑制血小板聚集。

警示用语:

Warning

危险分类

Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 2 - Carc. 2 - Eye Irrit. 2 - Met. Corr. 1 - Skin Irrit. 2 - Skin Sens. 1 - STOT RE 2 Oral

靶器官

spleen

储存分类代码

4.1A - Other explosive hazardous materials

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

法规信息

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分析证书(COA)

Lot/Batch Number

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PloS one, 9(6), e97973-e97973 (2014-06-03)
The human prostacyclin receptor (hIP receptor) is a seven-transmembrane G protein-coupled receptor (GPCR) that plays a critical role in vascular smooth muscle relaxation and platelet aggregation. hIP receptor dysfunction has been implicated in numerous cardiovascular abnormalities, including myocardial infarction, hypertension
Ayman M Atta et al.
International journal of molecular sciences, 16(4), 6911-6931 (2015-03-31)
In the present study, a new magnetic powder based on magnetite can be used as a petroleum crude oil collector. Amidoximes based on rosin as a natural product can be prepared from a reaction between hydroxylamine and rosin/acrylonitrile adducts. The
Marte S Dragset et al.
Antimicrobial agents and chemotherapy, 59(4), 2256-2264 (2015-02-04)
Efficient iron acquisition is crucial for the pathogenesis of Mycobacterium tuberculosis. Mycobacterial iron uptake and metabolism are therefore attractive targets for antitubercular drug development. Resistance mutations against a novel pyrazolopyrimidinone compound (PZP) that is active against M. tuberculosis have been

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