Name | L-Cysteic acid monohydrate |
Synonyms | CYSTEIC ACID, L-(RG) L-CYSTEIC ACID 1-HYDRATE L-Cysteic acid monohydrate L-Alanine,3-sulfo-,monohydrate (2R)-2-ammonio-3-sulfonatopropanoate 2-amino-3-sulfopropanoic acid hydrate 2-Amino-3-sulfopropionicacidmonohydrate (R)-2-Amino-3-sulfopropanoic acid hydrate L-Cysteic acid monohydrate,(R)-2-Amino-3-sulfopropionic acid |
CAS | 23537-25-9 |
EINECS | 207-861-3 |
InChI | InChI=1/C3H7NO5S/c4-2(3(5)6)1-10(7,8)9/h2H,1,4H2,(H,5,6)(H,7,8,9)/p-1/t2-/m0/s1 |
InChIKey | PCPIXZZGBZWHJO-DKWTVANSSA-N |
Molecular Formula | C3H9NO6S |
Molar Mass | 187.17 |
Melting Point | 267°C (dec.)(lit.) |
Water Solubility | Soluble in water. |
Solubility | H2O: soluble |
Appearance | Solid |
Color | White to Off-White |
Merck | 14,2780 |
BRN | 1725495 |
Storage Condition | Room Temperature |
Stability | Stable. Combustible. |
MDL | MFCD00149544 |
Physical and Chemical Properties | Colorless crystals, containing 1 molecule of crystal water is needle-like crystals. The anhydrous was decomposed at 260 °c. Soluble in water, insoluble in alcohol. |
Safety Description | S22 - Do not breathe dust. S24/25 - Avoid contact with skin and eyes. |
WGK Germany | 3 |
HS Code | 29379000 |
biological activity | L-Cysteic acid monohydrate (CAM) is an active endogenous metabolite. |
use | for organic synthesis. |
production method | cystine is dissolved in dilute hydrochloric acid, bromine is added dropwise, and the temperature of the reaction solution rises to about 60 ℃. The reaction liquid is evaporated under reduced pressure, the residue is dissolved in distilled water, and the insoluble matter is filtered out. After concentration, the filtrate is cooled and crystallized, filtered, the filter cake is washed with ethanol, and dried to obtain L-sulfoalanine with a yield of 81-90%. |