Molecular Formula | C2H6ClNO3 |
Molar Mass | 127.53 |
Density | 1.7848 (rough estimate) |
Melting Point | 156°C (dec.)(lit.) |
Boling Point | 326.7°C at 760 mmHg |
Flash Point | 151.4°C |
Water Solubility | decomposes |
Vapor Presure | 4.24E-05mmHg at 25°C |
Appearance | White crystal |
Color | White to off-white |
BRN | 3680528 |
Storage Condition | 2-8°C |
Sensitive | Easily absorbing moisture |
Refractive Index | 1.6500 (estimate) |
MDL | MFCD00012955 |
Physical and Chemical Properties | White crystals. Melting point 156 °c (decomposition). |
Use | It is used to introduce acidic groups into ketone compounds and can prepare chemiluminescent materials, such as preparing chemiluminescent substances ABEI labels on ketone compounds. It is also used as an inhibitor of transaminase. |
Hazard Symbols | Xi - Irritant |
Risk Codes | 36/37/38 - Irritating to eyes, respiratory system and skin. |
Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36 - Wear suitable protective clothing. |
WGK Germany | 3 |
RTECS | AF3150000 |
FLUKA BRAND F CODES | 3 |
HS Code | 29280000 |
Reference Show more | 1. Wang, Jieqi, et al. "Hydrophilic modification of PTFE microfiltration flat membrane by crosslinking OCMCS-PEI to enhance anti-fouling property." Progress in Organic Coatings 135 (2019): 565-573.https://doi.org/10.1016/j.porgcoat.2019.06.035 |
EPA chemical information | Information provided by: ofmpub.epa.gov (external link) |
biological activity | AOA hemihydrochloride (Aminooxyacetic acid, Carboxymethoxylamine, AOAA) is an inhibitor of aminobutyric acid transaminase (aminobutyrate aminotransferase), which is involved in the metabolism of amino acids and polyamines. |
Target | Value |
use | organic synthesis intermediate. It is used to introduce acidic groups into ketone compounds and can prepare chemiluminescent materials, such as preparing chemiluminescent substances ABEI labels on ketone compounds. It is also used as an inhibitor of transaminase. |
Production method | O-carboxymethylacetone oxime is obtained by reacting with hydrochloric acid. |