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M50400

Sigma-Aldrich

N-Methylhydroxylamine hydrochloride

98%

Sinônimo(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

Fórmula linear:
CH3NHOH · HCl
Número CAS:
4229-44-1
Peso molecular:
83.52
Beilstein:
3541409
Número CE:
224-181-2
Número MDL:
MFCD00012597
Código UNSPSC:
12352100
ID de substância PubChem:
24896973
NACRES:
NA.22

Nível de qualidade

200

Ensaio

98%

pf

86-88 °C (lit.)

cadeia de caracteres SMILES

Cl[H].CNO

InChI

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

chave InChI

RGZRSLKIOCHTSI-UHFFFAOYSA-N

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Categorias relacionadas

Aplicação

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

Pictogramas

Exclamation mark
GHS07

Palavra indicadora

Warning

Frases de perigo

H315,H319,H335

Declarações de precaução

P302 + P352 - P305 + P351 + P338

Classificações de perigo

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

Órgãos-alvo

Respiratory system

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

dust mask type N95 (US), Eyeshields, Gloves

Certificados de análise (COA)

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N-Benzylhydroxylamine hydrochloride puriss., ≥99.0% (AT)

Sigma-Aldrich

13454

N-Benzylhydroxylamine hydrochloride

Methoxyamine hydrochloride for GC derivatization, LiChropur™, 97.5-102.5% (AT)

Supelco

89803

Methoxyamine hydrochloride

N-Boc-O-tosylhydroxylamine 95%

Sigma-Aldrich

775037

N-Boc-O-tosylhydroxylamine

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
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
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
A Gibson et al.
British journal of pharmacology, 96(3), 637-644 (1989-03-01)
1. The effects of N-methylhydroxylamine (NMH) and of M&B 22948 on relaxations of the mouse anococcygeus to non-adrenergic, non-cholinergic (NANC) field stimulation and to a number of smooth muscle relaxant drugs were investigated. 2. Relaxations to NANC field stimulation (10
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