S-Benzoylthiamine O-monophosphate
S-Benzoylthiamine O-monophosphate (CAS: 22457-89-2) is a derivative of Thiamine (Vitamin B1). With the empirical formula C19H23N4O6PS and a molecular weight of 466.45 g/mol, this compound plays a role in biological research. Its applications are primarily within cell biology and nutrition research, contributing to studies related to vitamin metabolism and cellular functions. It is supplied by Tech Serve Solutions for laboratory and research purposes.
- IUPAC
- Benfotiamine
- Synonyms
- Benfotiamine
Cell Biology Research
Utilised in laboratory settings for investigating cellular processes and pathways. Its role as a thiamine derivative makes it valuable for understanding metabolic functions at the cellular level.
Nutrition Research
Applied in studies focusing on vitamin B1 metabolism and its physiological effects. Aids researchers in exploring the biochemical roles and requirements of thiamine in biological systems.
Biochemical Studies
Serves as a reagent in biochemical assays and experiments. Its specific structure allows for targeted investigations into enzymatic reactions or molecular interactions involving thiamine analogues.
| Molecular weight | 466.45 |
|---|---|
| Empirical formula | C19H23N4O6PS |
| Storage temperature | 2-8°C |
| Protective equipment | Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter |
|---|---|
| Water hazard class (WGK, DE) | 2 |
Hazard information is provided for guidance. Always consult the product Safety Data Sheet (SDS), available on request, before handling.
Documentation
Every batch ships with a Certificate of Analysis covering assay, identity and purity; the grade is confirmed against your enquiry. Safety Data Sheets and technical data sheets are available on request.
Supply & logistics
Samples for technical evaluation; bulk MOQ by grade and packaging. In-stock material ships in 7–10 working days, worldwide, with full export documentation.
What is S-Benzoylthiamine O-monophosphate used for?
+
S-Benzoylthiamine O-monophosphate is primarily used in cell biology and nutrition research. It serves as a reagent in biochemical studies and investigations into thiamine metabolism and cellular functions.
What are the CAS number and formula for S-Benzoylthiamine O-monophosphate?
+
The CAS number is 22457-89-2, and the empirical formula is C19H23N4O6PS.
What grade and purity does Tech Serve Solutions supply?
+
Tech Serve Solutions supplies this product for research purposes. The specific grade and purity (assay) are detailed on the product's Certificate of Analysis. We do not represent this product as USP, BP, EP, or pharmacopoeia grade unless explicitly stated in the specifications.
How should S-Benzoylthiamine O-monophosphate be handled?
+
Handle with appropriate personal protective equipment, including eyeshields and gloves. A type N95 (US) or type P1 (EN143) respirator filter is recommended. The compound is classified as WGK 2 in Germany, indicating it is hazardous to water.
How is S-Benzoylthiamine O-monophosphate shipped and exported?
+
Tech Serve Solutions is an experienced global supplier and exporter of fine chemicals, adhering to all necessary regulations for safe and compliant packaging, shipping, and export worldwide.
How can I request a sample or quote?
+
To request a sample or a quote for S-Benzoylthiamine O-monophosphate, please contact our sales department through the website or by phone, providing your specific requirements.
▶ Related products
(−)-Curcumol
C15H24O2
Cell Biology
(±) Clopidogrel hydrogensulfate
Cell Biology
(±)-L-Alliin
C6H11NO3S
Cell Biology
(±)-2-Amino-4-phosphonobutyric acid
C4H10NO5P
Cell Biology
(±)-2-Methylarachidonoyl-2′-fluoroethylamide
C23H38NOF
Cell Biology
(±)-3,4-Methylenedioxy-N-ethylamphetamine hydrochloride
Cell Biology
(±)-3,4-Methylenedioxyamphetamine hydrochloride
Cell Biology
(±)-3,4-Methylenedioxymethamphetamine hydrochloride
Cell Biology
▶ Explore more
3-Methyl-1,5-di-p-tolyl-1,4-pentazadiene
Chemical Synthesis
3-Methyl-1,5-pentanediol
Chemical Synthesis
3-Methyl-1-(2-methylphenyl)-1H-pyrazol-5-amine
C11H13N3
Chemical Synthesis
3-Methyl-1-(3′-sulfoamidophenyl)-5-pyrazolone
C10H11N3O3S
Chemical Synthesis