- Product Details
Keywords
- Benfotiamine
- 22457-89-2
- TIANFU CHEM Benfotiamine
Quick Details
- ProName: Newblue CHEM Benfotiamine
- CasNo: 22457-89-2
- Molecular Formula: C19H23N4O6PS
- Appearance: White powder
- Application: Pharmaceuticals
- DeliveryTime: according to client's demand quantity
- PackAge: as requested
- Port: SHANGHAI
- ProductionCapacity: 1 Metric Ton/Month
- Purity: 98%
- Storage: room temp
- Transportation: by sea, by air or by courier
- LimitNum: 1 Kilogram
Superiority
Our company was built in 2009 with an ISO certificate.
In the past 5 years, we have grown up as a famous fine chemicals supplier in China and we had established stable business relationships with Samsung,LG,Merck,Thermo Fisher Scientific and so on.
Our main business covers the fields below:
1.Noble Metal Catalysts (Pt.Pd...)
2.Organic Phosphine Ligands (Tert-butyl-phosphine.Cyclohexyl-phosphine...)
3.OLED intermediates (Fluorene,Carbazole,Boric acid...)
4.Customs Synthesis
Our advantage:
1.Higest quality and good package
2.Fast delivery
3.Better payment term
4.Fast response to customer within 6 hours
5.Good business credit in Europe ,US ,Japan ,Korea
Details
Benfotiamine Basic information
Product Name: Benfotiamine
Synonyms: benzoylthiamineo-monophosphate;berdi;betivina;bietamine;biotamin;btmp;neurostop;nitanevril
CAS: 22457-89-2
MF: C19H23N4O6PS
MW: 466.45
EINECS: 245-013-4
Product Categories: Aromatics;Heterocycles;Intermediates & Fine Chemicals;Pharmaceuticals;Phosphorylating and Phosphitylating Agents;Sulfur & Selenium Compounds;Pharmaceutical intermediate;BIOTAMIN;API
Mol File: 22457-89-2.mol
Benfotiamine Structure
Benfotiamine Chemical Properties
Melting point 165 C
storage temp. 2-8°C
CAS DataBase Reference 22457-89-2(CAS DataBase Reference)
Safety Information
Hazard Codes Xn
Risk Statements 20/21/22-36/37/38
Safety Statements 26-36
WGK Germany 2
RTECS DH6910000
Benfotiamine Usage And Synthesis
Chemical Properties crystals
Uses Vitamin B1 analog. Synthetic S-acyl derivative of Thiamine (T344185).
Definition ChEBI: A thioester that is a synthetic analogue of thiamine obtained by acylative cleavage of the thiazole ring and O-phospohorylation.