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Merck
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Documenti fondamentali

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M50400

Sigma-Aldrich

N-Methylhydroxylamine hydrochloride

98%

Sinonimo/i:

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

Formula condensata:
CH3NHOH · HCl
Numero CAS:
4229-44-1
Peso molecolare:
83.52
Beilstein:
3541409
Numero CE:
224-181-2
Numero MDL:
MFCD00012597
Codice UNSPSC:
12352100
ID PubChem:
24896973
NACRES:
NA.22

Livello qualitativo

200

Saggio

98%

Punto di fusione

86-88 °C (lit.)

Stringa SMILE

Cl[H].CNO

InChI

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

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Categorie correlate

Applicazioni

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

Pittogrammi

Exclamation mark
GHS07

Avvertenze

Warning

Indicazioni di pericolo

H315,H319,H335

Classi di pericolo

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

Organi bersaglio

Respiratory system

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves

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Certificati d'analisi (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

Bing Hao et al.
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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