Merck
CN

226904

Sigma-Aldrich

甲氧胺 盐酸盐

98%

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别名:
O-甲胲 盐酸盐, 甲氧基胺 盐酸盐
线性分子式:
CH3ONH2 · HCl
CAS号:
分子量:
83.52
Beilstein:
3589723
EC 号:
MDL编号:
PubChem化学物质编号:
NACRES:
NA.22

质量水平

检测方案

98%

形式

solid

mp

151-154 °C (lit.)

溶解性

alcohol: soluble(lit.)
water: soluble(lit.)

SMILES string

Cl.CON

InChI

1S/CH5NO.ClH/c1-3-2;/h2H2,1H3;1H

InChI key

XNXVOSBNFZWHBV-UHFFFAOYSA-N

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此商品
2749928980343504
Methoxyamine hydrochloride 98%

Sigma-Aldrich

226904

甲氧胺 盐酸盐

O-Ethylhydroxylamine hydrochloride 97%

Sigma-Aldrich

274992

O-乙基羟胺 盐酸盐

Methoxyamine hydrochloride for GC derivatization, LiChropur™, 97.5-102.5% (AT)

Supelco

89803

甲氧胺 盐酸盐

O-Ethylhydroxylamine hydrochloride for GC derivatization, LiChropur™

Supelco

43504

O-乙基羟胺 盐酸盐

form

solid

form

solid

form

crystals

form

-

mp

151-154 °C (lit.)

mp

130-133 °C (lit.)

mp

151-154 °C (lit.)

mp

130-133 °C (lit.)

solubility

alcohol: soluble(lit.), water: soluble(lit.)

solubility

-

solubility

-

solubility

-

一般描述

甲氧胺盐酸盐与人抗凝血酶III-凝血酶复合物结合,形成无活性的凝血酶

应用

甲氧基胺盐酸盐被用作制备 O-甲基肟的试剂。它还被用于由醛或酮合成 O-甲基肟。

警示用语:

Danger

危险分类

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

储存分类代码

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

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


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Edouard Godineau et al.
Organic letters, 8(21), 4871-4874 (2006-10-06)
[reaction: see text] A formal [2+2+2] process has been devised that allows the stereocontrolled formation of ring-fused piperidines from allylsilanes possessing an oxime moiety. The cascade involves an intermolecular radical addition of an alpha-iodoacetate onto an allylsilane double bond, which
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The Journal of Organic Chemistry, 59, 1492-1492 (1994)
M O Longas et al.
The Biochemical journal, 189(3), 481-489 (1980-09-01)
1. Cleavage of the human antithrombin III--thrombin complex with [14C]methoxyamine hydrochloride results in inactive thrombin and 14C-labelled antithrombin III. 2. Discontinuous polyacrylamide-gel electrophoresis of the reduced dissociation fragments of the complex in the presence of sodium dodecyl sulphate reveals two
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