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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
Assay:
98%
Form:
solid

Key Documents

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InChI key

XNXVOSBNFZWHBV-UHFFFAOYSA-N

InChI

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

SMILES string

Cl.CON

assay

98%

form

solid

Quality Level

200

solubility

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

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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.

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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

No data available

flash_point_c

No data available

ppe

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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

226904-BULK: + 226904-5G: + 226904-1G: + 226904-25G: + 226904-100G: + 226904-VAR:

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Certificates of Analysis (COA)

Lot/Batch Number
BCCG0204
BCCF2221
BCCC3195
WXBD0638V
BCCB7441

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The Journal of Organic Chemistry, 59, 1492-1492 (1994)
Synthesis, 849-849 (1992)
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
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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