Ritiometan

Base Information

• Chemical Name: Ritiometan
• CAS No.: 34914-39-1
• Molecular Formula: C7H10 O6 S3
• Molecular Weight: 286.351
• Hs Code.: 2930909090
• European Community (EC) Number: 252-284-2
• UNII: J89LM8QVEE
• DSSTox Substance ID: DTXSID50188468
• Nikkaji Number: J33.169D
• Wikipedia: Ritiometan
• Wikidata: Q7336743
• NCI Thesaurus Code: C74155
• Metabolomics Workbench ID: 154094
• ChEMBL ID: CHEMBL2105322
• Mol file: 34914-39-1.mol

Synonyms:Ritiometan;34914-39-1;Ritiometan [INN];Ritiometanum;2,2',2''-[methylidynetris(thio)]trisacetic acid;Ritiometanum [Latin];2-[bis(carboxymethylsulfanyl)methylsulfanyl]acetic acid;UNII-J89LM8QVEE;J89LM8QVEE;Ritiometan (INN);EINECS 252-284-2;2,2',2''-(Methylidynetris(thio))trisacetic acid;2-({bis[(carboxymethyl)sulfanyl]methyl}sulfanyl)acetic acid;(Methylidynetrithio)triacetic acid;RITIOMETAN [MART.];RITIOMETAN [WHO-DD];SCHEMBL867253;CHEMBL2105322;C7H10O6S3;DTXSID50188468;CHEBI:136023;C7-H10-O6-S3;DB13267;2,2,2-[methylidynetris(thio)]trisaceticacid;D07375;EN300-26205102;Q7336743;Acetic acid, 2,2',2''-(methylidynetris(thio))tris-

Chemical Property of Ritiometan

Chemical Property:

• Vapor Pressure: 2.64E-15mmHg at 25°C
• Boiling Point: 587.1°Cat760mmHg
• Flash Point: 308.9°C
• PSA: 187.80000
• Density: 1.681g/cm³
• LogP: 0.72340
• Storage Temp.: Hygroscopic, -20°C Freezer, Under inert atmosphere
• Solubility.: DMSO (Slightly), Methanol (Slightly)
• XLogP3: 1.2
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 9
• Rotatable Bond Count: 9
• Exact Mass: 285.96395156
• Heavy Atom Count: 16
• Complexity: 226

Purity/Quality:

98%Min ^*data from raw suppliers

Ritiometan ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C(C(=O)O)SC(SCC(=O)O)SCC(=O)O
• Uses: Ritiometan is an antibacterial that is used in nasal sprays.

Technology Process of Ritiometan

There total 2 articles about Ritiometan which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

formic acid (64-18-6) + mercaptoacetic acid (68-11-1) → methylidynetrithiotriacetic acid (34914-39-1)

Guidance literature:

With hydrogenchloride;

Reference yield:

formic acid (64-18-6) + mercaptoacetic acid (68-11-1) + (E)-3-Ureido-but-2-enoic acid ethyl ester (5435-44-9,22243-66-9) → methylidynetrithiotriacetic acid (34914-39-1)

Guidance literature:

upstream raw materials:

formic acid

mercaptoacetic acid

(E)-3-Ureido-but-2-enoic acid ethyl ester

Refernces