Key Documents

View All Documentation

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

Select a Size

Change View

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

Technical Service

Need help? Our team of experienced scientists is here for you.

Let Us Assist

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

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Articles

Glutamine Metabolism in Cancer Cells

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

许多癌细胞中的谷氨酰胺代谢失调

本文介绍了增殖活性细胞为何需要碳源和氮源合成大分子。尽管大部分肿瘤细胞利用有氧糖酵解途径并分流线粒体氧化磷酸化代谢物，但许多肿瘤细胞表现出线粒体活性增加。

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)

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)

View All Related Papers

Global Trade Item Number

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