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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
Beilstein:
3541409
EC Number:
224-181-2
MDL number:
MFCD00012597
UNSPSC Code:
12352100
PubChem Substance ID:
24896973
NACRES:
NA.22

Key Documents

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Quality Level

200

Assay

98%

mp

86-88 °C (lit.)

SMILES string

Cl[H].CNO

InChI

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

InChI key

RGZRSLKIOCHTSI-UHFFFAOYSA-N

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Application

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

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Precautionary Statements

P302 + P352 - P305 + P351 + P338

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

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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P S Brzović et al.
Biochemistry, 31(4), 1180-1190 (1992-02-04)
In an effort to understand the catalytic mechanism of the tryptophan synthase beta-subunit from Salmonella typhimurium, possible functional active site residues have been identified (on the basis of the 3-D crystal structure of the bienzyme complex) and targeted for analysis
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
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