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About This Item
Linear Formula:
CH3NHOH · HCl
CAS Number:
Molecular Weight:
83.52
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
224-181-2
Beilstein/REAXYS Number:
3541409
MDL number:
Assay:
98%
Quality Level
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
Application
Used to construct hydroxamates, important functional groups for the complexation of iron.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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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
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
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
Global Trade Item Number
| SKU | GTIN |
|---|---|
| M50400-10G | 04061834059455 |
| M50400-5G | 04061832768779 |
