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CAS RN: 25812-30-0 | Product Number: G0368
Gemfibrozil
Purity: >98.0%(GC)(T)
Synonyms:
- 2,2-Dimethyl-5-(2,5-dimethylphenoxy)pentanoic Acid
- 2,2-Dimethyl-5-(2,5-dimethylphenoxy)valeric Acid
Product Documents:
Size | Unit Price | Same Day | 2-3 Business Days | Quantity |
---|---|---|---|---|
5G |
S$73.50
|
10 | ≥60 |
|
25G |
S$243.00
|
1 | 11 |
|
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Product Number | G0368 |
Purity / Analysis Method | >98.0%(GC)(T) |
Molecular Formula / Molecular Weight | C__1__5H__2__2O__3 = 250.34 |
Physical State (20 deg.C) | Solid |
Storage Temperature | Room Temperature (Recommended in a cool and dark place, <15°C) |
CAS RN | 25812-30-0 |
Reaxys Registry Number | 1881200 |
PubChem Substance ID | 125307848 |
SDBS (AIST Spectral DB) | 52970 |
Merck Index (14) | 4388 |
MDL Number | MFCD00079335 |
Specifications
Appearance | White to Almost white powder to crystal |
Purity(GC) | min. 98.0 % |
Purity(Neutralization titration) | min. 98.0 % |
Melting point | 57.0 to 62.0 °C |
Properties (reference)
Melting Point | 61 °C |
Boiling Point | 159 °C/0.02 mmHg |
Solubility (soluble in) | Methanol |
GHS
Pictogram | |
Signal Word | Warning |
Hazard Statements | H302 : Harmful if swallowed. H413 : May cause long lasting harmful effects to aquatic life. |
Precautionary Statements | P501 : Dispose of contents/ container to an approved waste disposal plant. P273 : Avoid release to the environment. P270 : Do not eat, drink or smoke when using this product. P264 : Wash skin thoroughly after handling. P301 + P312 + P330 : IF SWALLOWED: Call a POISON CENTER/doctor if you feel unwell. Rinse mouth. |
Related Laws:
RTECS# | YV7120000 |
Transport Information:
H.S.code* | 2918.99-000 |
Application
Gemfibrozil: An Antilipemic Fibrate
The fibrates, including gemfibrozil, are lower elevated serum lipids by decreasing the low density lipoprotein (LDL) fraction rich in cholesterol and the very low density lipoprotein (VLDL) fraction rich in triglycerides. In addition, fibrates increase the high density lipoprotein (HDL) cholesterol fraction. The precise mechanisms of action remain unknown, but it has been reported that the major modes of action of the fibrates as follows: VLDL catabolism by increased lipoprotein and hepatic triglyceride lipase activities; suppression of triglyceride biosynthesis by acetyl-CoA carboxylase enzyme inhibition and attenuation of cholesterol biosynthesis by inhibition of the rate-limiting HMG-CoA reductase. In 2000s, it has been reported that concomitant use of gemfibrozil with statins (in particular cerivastatin) increases the risk of rhabdomyolysis which is a serious syndrome due to a muscle injury. (The product is for research purpose only.)
References
- Gemfibrozil. A review of its pharmacodynamic and pharmacokinetic properties, and therapeutic use in dyslipidemia
- Gemfibrozil: a reappraisal of its pharmacological properties and place in the management of dyslipidemia
- Atorvastatin and gemfibrozil metabolites, but not the parent drugs, are potent antioxidants against lipoprotein oxidation
- Gemfibrozil greatly increases plasma concentrations of cerivastatin
- Simultaneous quantitation of rosuvastatin and gemfibrozil in human plasma by high-performance liquid chromatography and its application to a pharmacokinetic study
- A high performance liquid chromatography method for simultaneous determination of rosiglitazone and gemfibrozil in human plasma
PubMed Literature
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