(Aminooxy)Acetic Acid Hemihydrochloride

(Aminooxy)Acetic Acid Hemihydrochloride

Synonyms O-(Carboxymethyl)hydroxylamine hemihydrochloride; (Carboxymethoxy)amine hemihydrochloride; Hydroxylamine-O-acetic acid hemihydrochloride; Carboxymethoxylamine

CAS Number: 2921-14-4 Molecular Formula: C2H5NO3·1/2HCl Molecular Weight: 218.59 g/mol

Beilstein Registry Number: 3680528 EC Number: 220-862-3 MDL Number: MFCD00012955

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SKU 02150104-CF
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Description

Product Description

(Aminooxy)Acetic Acid Hemihydrochloride

Application Notes

(Aminooxy)acetic Acid Hemihydrochloride undergoes condensation with aldehydes and ketones to form oximes. It inhibits aminobutyrate aminotransferase activity in vivo, thereby raising the level of gamma-aminobutyric acid in tissues.

Usage Statement

Research Use Only (RUO). Ready for CE IVD labeling of clinical applications.

Key Applications

Inhibits aminobutyrate aminotransferase activity

Specifications
SKU 02150104-CF
Application Notes (Aminooxy)acetic Acid Hemihydrochloride undergoes condensation with aldehydes and ketones to form oximes. It inhibits aminobutyrate aminotransferase activity in vivo, thereby raising the level of gamma-aminobutyric acid in tissues.
Beilstein Registry Number 3680528
EC Number 220-862-3
Format Crystalline powder
Hazard Statements H315-H319-H335
Applications Inhibits aminobutyrate aminotransferase activity
Molecular Formula C2H5NO3·1/2HCl
Molecular Weight 218.59 g/mol
Personal Protective Equipment Dust mask, Eyeshields, Gloves
Physical Appearance White Crystalline Powder
Product Families Description (Aminooxy)acetic acid
Product Overview (Aminooxy)Acetic Acid Hemihydrochloride
RTECS Number AF3150000
Safety Symbol GHS07
Storage and Handling Store at Room Temperature (15-30 °C). Store Desiccated.
Usage Statement Research Use Only (RUO). Ready for CE IVD labeling of clinical applications.