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Merck

226904

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
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24853598
EC Number:
209-798-7
Beilstein/REAXYS Number:
3589723
MDL number:
MFCD00012951

Product Name

Methoxyamine hydrochloride, 98%

InChI key

XNXVOSBNFZWHBV-UHFFFAOYSA-N

InChI

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

SMILES string

Cl.CON

assay

98%

form

solid

mp

151-154 °C (lit.)

solubility

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

Quality Level

200

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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.

General description

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

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

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

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

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Certificates of Analysis (COA)

Lot/Batch Number
BCCP0922
BCCN4399
WXBF5819V
BCCM1056
BCCM6272

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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
Tetrahedron Letters, 47, 6045-6045 (2006)
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
Synthesis, 849-849 (1992)
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