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C13408

O-(Carboxymethyl)hydroxylamine hemihydrochloride

Name: <I>O</I>-(Carboxymethyl)hydroxylamine hemihydrochloride
Brand: ALDRICH

98%

Synonym(s):

Carboxymethoxylamine hemihydrochloride, (Aminooxy)acetic acid hemihydrochloride, (Carboxymethoxy)amine hemihydrochloride, Hydroxylamine-O-acetic acid hemihydrochloride

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About This Item

Linear Formula:

NH₂OCH₂COOH · 0.5HCl

CAS Number:

2921-14-4

Molecular Weight:

109.30

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24892403

EC Number:

220-862-3

Beilstein/REAXYS Number:

3680528

MDL number:

MFCD00012955

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Properties

biological source

synthetic (organic)

Quality Level

200

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

Description

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

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Glutamine Metabolism in Cancer Cells

Sigma article discusses tumor cell metabolic pathways, focusing on aerobic glycolysis and mitochondrial activity.

Synthesis and in vitro antibacterial properties of 2-(3-bromo-5-isoxazolylideneamino-oxy)acetamido-beta-lactam derivatives.

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.

Tetrahedron Letters, 34, 4347-4347 (1993)

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)

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Global Trade Item Number

SKU	GTIN
C13408-10G	04061833467367
C13408-1G	04061833467374
C13408-25G	04061832104959