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Thiazolidine-4-carboxylic acid

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Thiazolidine-4-carboxylic acid manufacturers

  • Timonacic
  • Timonacic pictures
  • $29.00
  • 2026-05-11
  • CAS:444-27-9
  • Purity: 99.99%
  • Supply Ability: 10g
  • Timonacic
  • Timonacic pictures
  • $29.00
  • 2026-05-11
  • CAS:444-27-9
  • Purity: 99.99%
  • Supply Ability: 10g
Thiazolidine-4-carboxylic acid Basic information
Product Name:Thiazolidine-4-carboxylic acid
Synonyms:t-4ca;usafa-3701;THIAZOLIDINE-4-CARBOXYLIC ACID;1,3-THIAZOLIDINE-4-CARBOXYLIC ACID;AKOS BBS-00007512;AURORA 619;Thioproline Crystalline;L-Hepalidine
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 Structure
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
pka2.09±0.20(Predicted)
color White to off-white
Water Solubility 29.3g/L(21 ºC)
Cosmetics Ingredients FunctionsSKIN CONDITIONING
InChIInChI=1S/C4H7NO2S/c6-4(7)3-1-8-2-5-3/h3,5H,1-2H2,(H,6,7)
InChIKeyDZLNHFMRPBPULJ-UHFFFAOYSA-N
SMILESS1CC(C(O)=O)NC1
CAS DataBase Reference444-27-9(CAS DataBase Reference)
EPA Substance Registry System4-Thiazolidinecarboxylic acid (444-27-9)
Safety Information
RIDADR 2811
TSCA TSCA listed
HazardClass 6.1(b)
PackingGroup III
MSDS Information
ProviderLanguage
1,3-Thiazolidine-4-carboxylic acid English
Thiazolidine-4-carboxylic acid Usage And Synthesis
OriginatorHepaldine,Riker,France,1964
Useshepatoprotectant
UsesTimonacic 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.
DefinitionChEBI: A sulfur-containing amino acid that is proline in which the methylene group at position 4 is replaced by a sulfur atom.
Manufacturing ProcessCysteine 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 FunctionHepatoprotectant, Choleretic
Thiazolidine-4-carboxylic acid Preparation Products And Raw materials
Raw materialsSodium hydroxide-->Formaldehyde-->L-Cysteine
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