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Merck
CN

M50400

N-Methylhydroxylamine hydrochloride

98%

Synonym(s):

Methylhydroxylammonium chloride, N-Hydroxy-N-methanamine hydrochloride, N-Hydroxy-N-methylammonium chloride, N-Hydroxymethanamine hydrochloride, N-Hydroxymethylamine hydrochloride, N-Methylhydroxyamine hydrochloride, N-Methylhydroxylamine monohydrochloride, N-Methylhydroxylammonium chloride

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About This Item

Linear Formula:
CH3NHOH · HCl
CAS Number:
4229-44-1
Molecular Weight:
83.52
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24896973
EC Number:
224-181-2
Beilstein/REAXYS Number:
3541409
MDL number:
MFCD00012597
Assay:
98%

Key Documents

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Product Name

N-Methylhydroxylamine hydrochloride, 98%

InChI key

RGZRSLKIOCHTSI-UHFFFAOYSA-N

InChI

1S/CH5NO.ClH/c1-2-3;/h2-3H,1H3;1H

SMILES string

Cl[H].CNO

assay

98%

mp

86-88 °C (lit.)

Quality Level

200

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Application

Used to construct hydroxamates, important functional groups for the complexation of iron.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
SDBB3656
STBL2683
STBK9781
STBJ7422
STBJ7002

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S L Martins et al.
European journal of pharmacology, 284(3), 265-270 (1995-09-25)
The effects of the K+ channel blockers, apamin, tetraethylammonium and 4-aminopyridine, upon the relaxations of the isolated rat proximal duodenum induced by nitregic nerve activation, nitric oxide (NO), the NO donor 3-morpholinosydnonimine (SIN-1) and Br-cyclic GMP were determined. The effects
Chunmei Geng et al.
ACS omega, 6(1), 358-366 (2021-01-19)
Doxorubicin (DOX) is widely used to treat solid tumors, but its use is limited by its severe cardiotoxicity, nephrotoxicity, hepatotoxicity, and neurotoxicity. Metabolomic studies on DOX-induced toxicity are mainly focused on alterations in the heart and kidney, but systematic research
Liang Zhao et al.
Chemistry, an Asian journal, 1(1-2), 203-209 (2007-04-19)
The three-component reaction of N-substituted hydroxylamines, aldehydes, and phenylacetylene catalyzed by CuCl/2,2'-bipyridine in the presence of NaOAc under neat conditions afforded the corresponding beta-lactams in good to excellent yields. Aromatic, heteroaromatic, and aliphatic aldehydes are tolerated in this reaction. The
Inorganic Chemistry, 32, 1467-1467 (1993)
Diversity of the E2P phosphoforms of Na,K-ATPase.
N U Fedosova et al.
Annals of the New York Academy of Sciences, 834, 386-389 (1998-02-12)
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