Newblue CHEM Benfotiamine

Min.Order / FOB Price:Get Latest Price

1 Kilogram	Negotiable

1 Kilogram

Negotiable

Min.Order :1 Kilogram
Purity: 98%
Payment Terms : L/C,D/A,D/P,T/T,

Keywords

Benfotiamine 22457-89-2 TIANFU CHEM Benfotiamine

Quick Details

Appearance:White powder
Application:Pharmaceuticals
PackAge:as requested
ProductionCapacity:1|Metric Ton|Month
Storage:room temp
Transportation:by sea, by air or by courier

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.

View All

Visit Store