Thiazolidine-4-carboxylic acid
Thiazolidine-4-carboxylic acid Basic information
- Product Name:
- Thiazolidine-4-carboxylic acid
- Synonyms:
-
- t-4ca
- usafa-3701
- TIMONACIC
- THIOPROLINE
- THIAZOLIDINE-4-CARBOXYLIC ACID
- 1,3-THIAZOLIDINE-4-CARBOXYLIC ACID
- AKOS BBS-00007512
- AURORA 619
- CAS:
- 444-27-9
- MF:
- C4H7NO2S
- MW:
- 133.17
- EINECS:
- 207-146-6
- Product Categories:
-
- Heterocyclic Compounds
- DETOXEPA
- API
- Mol File:
- 444-27-9.mol
Thiazolidine-4-carboxylic acid Chemical Properties
- Melting point:
- 196.5°C
- Boiling point:
- 350.3±37.0 °C(Predicted)
- Density
- 1.226 (estimate)
- refractive index
- 1.5480 (estimate)
- storage temp.
- Room Temperature
- solubility
- DMSO (Slightly), Water (Slightly)
- form
- solid
- pka
- 2.09±0.20(Predicted)
- color
- White to off-white
- Water Solubility
- 29.3g/L(21 ºC)
- CAS DataBase Reference
- 444-27-9(CAS DataBase Reference)
- EPA Substance Registry System
- 4-Thiazolidinecarboxylic acid (444-27-9)
MSDS
- Language:English Provider:1,3-Thiazolidine-4-carboxylic acid
Thiazolidine-4-carboxylic acid Usage And Synthesis
Originator
Hepaldine,Riker,France,1964
Uses
hepatoprotectant
Uses
Timonacic is a derivative of Proline (P756050), a cyclic nonessential amino acid. Timonacic is a research molecule of interest with potential antineoplastic activities by acting on the cell membrane of tumour cells and causing reverse transformation to normal cells.
Definition
ChEBI: A sulfur-containing amino acid that is proline in which the methylene group at position 4 is replaced by a sulfur atom.
Manufacturing Process
Cysteine is first dissolved in distilled water which has been freed of oxygen by boiling. Formaldehyde of 30% (w/v) concentration is added while stirring and the temperature of the mixture rises, while the thiazolidine carboxylic acid begins crystallizing. The stirring is continued for 2 hours after which ethyl alcohol of 95% (w/v) concentration is added to induce further crystallization. The mixture is left to stand for 24 hours at 4°C. The mixture is then filtered with retention of a crude product, which is purified by recrystallization from boiling distilled water. The crystals are then dried at about 40°C. The free acid is then converted to the sodium salt with NaOH.
Therapeutic Function
Hepatoprotectant, Choleretic
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