Lipids and Lipid Derivatives
eMolecules 94-96-2 | 2-Ethyl-1,3-hexanediol | Combi-Blocks, Inc. | MFCD00004578 | 146.230 | C8H18O2 | 97.000 | CCCC(O)C(CC)CO | 25g | 603131793
2-Ethyl-1,3-hexanediol | Combi-Blocks, Inc. | 94-96-2 | MFCD00004578 | 146.230 | C8H18O2 | 97.000 | CCCC(O)C(CC)CO | 25g | 603131793
AdipoGen 8-Phenyl-1-octanol (5 g)
Chemical. CAS: 10472-97-6. Formula: C14H22O. MW: 206.3. Synthetic. Primary alcohol building block for synthesis.
Sigma Aldrich Fine Chemicals Biosciences Retinol BioXtra, >=97.5% (HPLC), ~3100 U/mg | 68-26-8 | MFCD00001552 | 1G
Retinol BioXtra, >=97.5% (HPLC), ~3100 U/mg | Purity: >=97.5% (HPLC) | Mol Wt: 286.45 | 68-26-8 | MFCD00001552 | 1G
Echelon Biosciences Research Labs 2Z,6Z FARNESOL 50 mg
Isoprenoids and isoprenols are key metabolic intermediates for biosynthesis of steroids, including cholesterol and hormones that regulate human reproduction or fertility, and post-translational modifications of proteins in signal transduction pathways for cell division and regulation of vesicular trafficking. This item is non returnable
AdipoGen 8-Phenyl-1-octanol (1 g)
Chemical. CAS: 10472-97-6. Formula: C14H22O. MW: 206.3. Synthetic. Primary alcohol building block for synthesis.
Chem-Impex International, Inc. 2-Deoxy-D-glucose | MFCD00151328 | 5G
2-Deoxy-D-glucose, MFCD00151328, 5G
Accela Chembio Inc 1 | 7-heptanediol | 100g | 629-30-1 | MFCD00002987 | 97+% | D: 0.951 | Shelf Life: 900 Days | Regular
1 | 7-heptanediol | 100g | 629-30-1 | MFCD00002987 | 97+% | D: 0.951 | Shelf Life: 900 Days | Regular
Medchemexpress LLC All-trans-Anhydro Retinol (Anhydrovitamin A) | 1224-78-8 | 10 MG
All-trans-Anhydro Retinol (Anhydrovitamin A) is an orally active degradation product formed by the dehydration of vitamin A alcohol and its esters under conditions such as acidic catalysis or hydroxylic solvents. Its biological activity is only 0.4% of that of Vitamin A. In rats, it can be metabolized into hydroxy derivatives and their esters, but it cannot be converted into Vitamin A and has a low storage capacity in the body.
- Orally active degradation product of vitamin A
- Biological activity is 0.4% of vitamin A
- Metabolized into hydroxy derivatives; not converted to vitamin A
- Low storage capacity in the body
- Ships with dry ice
- Store at -80°C, protect from light, and under nitrogen
- Soluble in DMSO (10 mg/mL)
eMolecules 31502-14-4 | TRANS-2-NONEN-1-OL | AstaTech | MFCD00014058 | 142.242 | C9H18O | 93.000 | CCCCCC\C=C\CO | 1g | 718084806
TRANS-2-NONEN-1-OL | AstaTech | 31502-14-4 | MFCD00014058 | 142.242 | C9H18O | 93.000 | CCCCCC\C=C\CO | 1g | 718084806
eMolecules 13038-21-6 | 8-Nonen-1-ol | MFCD00798062 | 1g
Pharmablock | 4-bromoisoxazol-3-amine | 25mg | 784549076 | PBUD031 | 1519318-68-3 | MFCD21952501 | 162.974 | C3H3BrN2O
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eMolecules Building Block Tool
eMolecules 74462-02-5 | Ambeed | 44-(2-Ethylhexane-11-diyl)diphenol | 1g | 714082432 | A129839 | MFCD08276371 | 298.426 | C20H26O2
Ambeed | 44-(2-Ethylhexane-11-diyl)diphenol | 1g | 714082432 | A129839 | 74462-02-5 | MFCD08276371 | 298.426 | C20H26O2
Sigma Aldrich Fine Chemicals Biosciences 1-Octanol suitable for HPL1L
1OCTANOL45 1-Octanol suitable for HPL1L
Cayman Chemical 12 13DiHOME Fatty Acids and De
A diol form of (±)12,13-EpOME; toxic to Sf21 cells expressing sEH and to lacZ-expressing control cells; rat spinal cord levels are increased following burn injury; BALF levels are elevated in humans following exposure to biodiesel exhaust and in exhaled breath condensate in patients with allergic asthma following allergen exposure; plasma levels are increased immediately following moderate-intensity exercise in mice and humans
[C@@H](N)COP([O-])(=O)OCC[N+](C)(C)C | 5mg | 779524238](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502473542.JPG-250.jpg)
eMolecules 1670-26-4 | D-erythro Lysosphingomyelin (d18:1) | Broadpharm | MFCD02259287 | 464.628 | C23H49N2O5P | 0.000 | CCCCCCCCCCCCC\C=C\[C@@H](O)[C@@H](N)COP([O-])(=O)OCC[N+](C)(C)C | 5mg | 779524238
D-erythro Lysosphingomyelin (d18:1) | Broadpharm | 1670-26-4 | MFCD02259287 | 464.628 | C23H49N2O5P | 0.000 | CCCCCCCCCCCCC\C=C\[C@@H](O)[C@@H](N)COP([O-])(=O)OCC[N+](C)(C)C | 5mg | 779524238