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Merck
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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

Escolha uma das versões mais recentes:

Certificados de análise (COA)

Lot/Batch Number
STBJ7422
STBJ7002
STBH4485
STBH2313
STBG9948

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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

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Chemistry & biology, 11(9), 1317-1324 (2004-09-24)
L-pyrrolysine, the 22(nd) genetically encoded amino acid, was previously deduced to be (4R, 5R)-4-substituted-pyrroline-5-carboxylate attached to the epsilon-nitrogen of lysine based on the crystal structure of the M. barkeri monomethylamine methyltransferase (MtmB). To confirm L-pyrrolysine's identity, structures of MtmB have
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
G Garthwaite et al.
Neuroscience, 26(1), 321-326 (1988-07-01)
Incubated slices of young rat cerebellum were used to examine the possible relationship between the neurotoxic effects of excitatory amino acids and their ability to elicit large increases in the levels of cyclic GMP in this tissue. No cell death
Xuemei Ye et al.
BioMed research international, 2018, 3128270-3128270 (2018-11-10)
Linezolid has been widely used in serious infections for its effective inhibiting effect against multidrug-resistant gram-positive pathogens. However, linezolid caused severe adverse reactions, such as thrombocytopenia, anaemia, optic neuropathy, and near-fatal serotonin syndrome. In order to investigate the toxicity of
Jun Xie et al.
Chinese journal of integrative medicine, 25(5), 348-353 (2016-12-29)
To investigate the effects of Pinggan Prescription (, PGP) on hypertension by the associated methods of metabonomic and pharmacodynamic. A total of 32 male spontaneously hypertensive rats (SHRs) were randomly divided into two groups by using the random number table
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