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线性分子式:
CH3NHOH · HCl
化学文摘社编号:
分子量:
83.52
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
224-181-2
Beilstein/REAXYS Number:
3541409
MDL number:
产品名称
N-甲基羟胺 盐酸盐, 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
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Application
用于形成异羟肟酸盐,这是用于铁络合的重要官能团
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Inorganic Chemistry, 32, 1467-1467 (1993)
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
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)
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
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
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