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226904

Sigma-Aldrich

Methoxyamine hydrochloride

98%

Synonym(s):

O-Methylhydroxylamine hydrochloride, Methoxylamine hydrochloride

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About This Item

Linear Formula:
CH3ONH2 · HCl
CAS Number:
593-56-6
Molecular Weight:
83.52
Beilstein/REAXYS Number:
3589723
EC Number:
209-798-7
MDL number:
MFCD00012951
UNSPSC Code:
12352100
PubChem Substance ID:
24853598
NACRES:
NA.22

assay

98%

form

solid

mp

151-154 °C (lit.)

solubility

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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General description

Methoxyamine hydrochloride combines with human antithrombin III-thrombin complex to form an inactive thrombin.

Application

Methoxyamine hydrochloride was used as a reagent in the preparation of O-methyl oximes. It was also used in the synthesis of O-methyl oximes from aldehydes or ketones.

signalword

Danger

Hazard Classifications

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

Storage Class

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

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

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

Certificates of Analysis (COA)

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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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[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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