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(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

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

Unless specified otherwise, MP Biomedical's products are for research or further manufacturing use only, not for direct human use. For more information, please contact our customer service department.

Key Applications

Inhibits aminobutyrate aminotransferase activity

Specifications
SKU 02150104-CF
Alternate Names O-(Carboxymethyl)hydroxylamine hemihydrochloride; (Carboxymethoxy)amine hemihydrochloride; Hydroxylamine-O-acetic acid hemihydrochloride; Carboxymethoxylamine
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.
Base Catalog Number 150104
Beilstein Registry Number 3680528
CAS # 2921-14-4
EC Number 220-862-3
Format Crystalline powder
Hazard Statements H315-H319-H335
Molecular Formula C2H5NO3·1/2HCl
Molecular Weight 218.59 g/mol
Personal Protective Equipment Dust mask, Eyeshields, Gloves
RTECS Number AF3150000
Safety Symbol GHS07
Usage Statement Unless specified otherwise, MP Biomedical's products are for research or further manufacturing use only, not for direct human use. For more information, please contact our customer service department.