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Merck
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文件

226904

Sigma-Aldrich

甲氧胺 盐酸盐

98%

别名:

O-甲胲 盐酸盐, 甲氧基胺 盐酸盐

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About This Item

线性分子式:
CH3ONH2 · HCl
CAS号:
593-56-6
分子量:
83.52
Beilstein:
3589723
EC號碼:
209-798-7
MDL號碼:
MFCD00012951
分類程式碼代碼:
12352100
PubChem物質ID:
24853598
NACRES:
NA.22

化驗

98%

形狀

solid

mp

151-154 °C (lit.)

溶解度

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

SMILES 字串

Cl.CON

InChI

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

InChI 密鑰

XNXVOSBNFZWHBV-UHFFFAOYSA-N

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相关类别

一般說明

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。

應用

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。

訊號詞

Danger

危險分類

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

儲存類別代碼

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

水污染物質分類（WGK）

WGK 3

閃點（°F）

Not applicable

閃點（°C）

Not applicable

個人防護裝備

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

分析证书(COA)

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核糖醇 ≥99%

Sigma-Aldrich

A5502

核糖醇

N,O-二甲基羟胺 盐酸盐 98%

Sigma-Aldrich

D163708

N,O-二甲基羟胺 盐酸盐

吡啶 anhydrous, 99.8%

Sigma-Aldrich

270970

吡啶

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
Jean-Philippe Mevy et al.
Plants (Basel, Switzerland), 9(9) (2020-09-10)
Global change scenarios in the Mediterranean basin predict a precipitation reduction within the coming hundred years. Therefore, increased drought will affect forests both in terms of adaptive ecology and ecosystemic services. However, how vegetation might adapt to drought is poorly
The Journal of Organic Chemistry, 59, 1492-1492 (1994)
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
Tetrahedron Letters, 47, 6045-6045 (2006)
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