(Aminooxy) Acetic acid hemihydrochloride
(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
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 | C2H5NO3ยท1/2HCl |
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. |