C13408
O-(Carboxymethyl)hydroxylamine hemihydrochloride
98%
Synonym(s):
Carboxymethoxylamine hemihydrochloride, (Aminooxy)acetic acid hemihydrochloride, (Carboxymethoxy)amine hemihydrochloride, Hydroxylamine-O-acetic acid hemihydrochloride
Sign In to View Organizational & Contract Pricing.
Select a Size
Change View
About This Item
Linear Formula:
NH2OCH2COOH · 0.5HCl
CAS Number:
Molecular Weight:
109.30
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
220-862-3
Beilstein/REAXYS Number:
3680528
MDL number:
biological source
synthetic (organic)
assay
98%
form
crystalline powder, powder or crystals
mp
156 °C (dec.) (lit.)
solubility
water: 100 mg/mL, clear to slightly hazy, colorless to faintly yellow
storage temp.
2-8°C
SMILES string
Cl.NOCC(O)=O.NOCC(O)=O
InChI
1S/2C2H5NO3.ClH/c2*3-6-1-2(4)5;/h2*1,3H2,(H,4,5);1H
InChI key
KBXIJIPYZKPDRU-UHFFFAOYSA-N
Application
O-(Carboxymethyl)hydroxylamine hemihydrochloride can be used as a reactant to synthesize oximes via condensation with aldehydes and ketones . It can also be used as a potent inhibitor of (pyridoxal 5’-phosphate) PLP-dependent β-lyases .
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
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Tissue distribution of cytosolic beta-elimination reactions of selenocysteine Se-conjugates in rat and human
Rooseboom M, et al.
Chemico-Biological Interactions, 140, 243-264 (2002)
Characterization of a 5'-aldehyde terminus resulting from the oxidative attack at C5 `of a 2-deoxyribose on DNA
Angeloff A, et al.
Chemical Research in Toxicology, 14, 1413-1420 (2001)
A Sala et al.
Farmaco (Societa chimica italiana : 1989), 46(7-8), 887-897 (1991-07-01)
The synthesis of new 2-(3-bromo-5-isoxazolylideneamino-oxy)acetic acids and their condensation derivatives with suitable beta-lactam nuclei is reported. Their antibacterial properties have been tested in vitro. An interesting activity against Gram-positive bacteria including beta-lactamase-producing microorganisms was found among the cephalosporanic acid derivatives.