Basic information Safety Supplier Related

Thiazolidine-4-carboxylic acid

Basic information Safety Supplier Related

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
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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)
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Safety Information

RIDADR 
2811
HazardClass 
6.1(b)
PackingGroup 
III

MSDS

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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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