Thiamine triphosphorate

Base Information

• Chemical Name: Thiamine triphosphorate
• CAS No.: 3475-65-8
• Molecular Formula: C12H19 N4 O10 P3 S
• Molecular Weight: 504.291
• Wikipedia: Thiamine_triphosphate
• Wikidata: Q3523978
• Mol file: 3475-65-8.mol

Synonyms:Thiamin Triphosphate;Thiamine Triphosphate;Triphosphate, Thiamin;Triphosphate, Thiamine

Chemical Property of Thiamine triphosphorate

Chemical Property:

• PSA: 276.73000
• LogP: 1.32700
• XLogP3: -2.3
• Hydrogen Bond Donor Count: 4
• Hydrogen Bond Acceptor Count: 14
• Rotatable Bond Count: 10
• Exact Mass: 504.00347498
• Heavy Atom Count: 30
• Complexity: 726

Purity/Quality:

98%Min ^*data from raw suppliers

ThiamineTriphosphate ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC1=C(SC=[N+]1CC2=CN=C(N=C2N)C)CCOP(=O)(O)OP(=O)(O)OP(=O)(O)[O-]
• Uses: Thiamine Triphosphate is a derivative of Thiamine (T344185) which is a essential nutrient required for carbohydrate metabolism.

Technology Process of Thiamine triphosphorate

There total 1 articles about Thiamine triphosphorate 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:

→ thiamine triphosphate (3475-65-8)

Guidance literature:

Thiaminchlorid-hydrochlorid, H3PO4, Phosphoranhydrid <30 min, 95-100grad>;

Reference yield:

naphthalene (91-20-3,71998-51-1,72931-45-4) + thiamine triphosphate (3475-65-8) → cis-decalin (493-01-6)

Guidance literature:

at 100 - 120 ℃;

Reference yield:

thiamine triphosphate (3475-65-8) + butanone (78-93-3) → iso-butanol (78-92-2,15892-23-6)

Guidance literature:

Hydrogenation;

Downstream raw materials:

2-methyltetrahydrofuran

thiamine monophosphate chloride

4-methyl-3-(2-methyl-6-oxo-1,6-dihydro-pyrimidin-5-ylmethyl)-5-(2-phosphonooxy-ethyl)-thiazolium; chloride

3-(4-amino-2-methyl-pyrimidin-5-ylmethyl)-4-methyl-5-(2-phosphonooxy-ethyl)-thiazolium; hydrochloride

Refernces