Lipids and Lipid Derivatives
Medchemexpress LLC Oleic acid (9-cis-Octadecenoic acid) | 112-80-1 | 282.46 | 1 ML
Oleic acid is an abundant monounsaturated fatty acid and a Na+/K+ ATPase activator.
- High purity of 99.97%.
- Appears as a solid below 13°C and a liquid above 14°C.
- Colorless to light yellow.
- Soluble in ethanol, 0.1 M NaOH, and DMSO.
- Classified as ketones, aldehydes, and acids.
- Derived from an endogenous metabolite.
- Ships at room temperature in the continental US.
- Storage conditions vary based on form: -20°C for 3 years (pure) or -80°C for 6 months (in solvent).
Cayman Chemical 15-methyl PalmItIc AcId 20mg
A methylated fatty acid; has been found in bacteria, bovine milk fat, one-humped camel meat and fat, and in rabbit perirenal lipids; found in human breast milk and levels are decreased in mature breast milk compared to colostrum
Cayman Chemical OleIc nhydrIde 250mg
A fatty acid anhydride; inhibits sphingosine-induced phosphorylation of p32 in Jurkat T cells from 30-100 μM; has been used in the synthesis of various phospholipids and triglycerides
Medchemexpress LLC Palmitic acid-d4-1 | 75736-47-9 | 260.45 | 50 MG
Palmitic acid-d4-1 is a stable isotope of palmitic acid, identified by the CAS number 75736-47-9. This chemical is supplied as a solid with a melting point range of 60-63°C and a molecular weight of 260.45. It is stable under recommended storage conditions and is intended for use as a laboratory chemical in the manufacture of substances.
- Solid appearance
- Stable under recommended storage conditions
- Suitable for laboratory chemical applications
- Melting point 60-63°C
eMolecules 57-10-3 | Palmitic acid | Oakwood Chemical | MFCD00002747 | 256.430 | C16H32O2 | 99.000 | CCCCCCCCCCCCCCCC(O)=O | 5g | 537716738
Palmitic acid | Oakwood Chemical | 57-10-3 | MFCD00002747 | 256.430 | C16H32O2 | 99.000 | CCCCCCCCCCCCCCCC(O)=O | 5g | 537716738
eMolecules 57-10-3 | Hexadecanoic acid | Combi-Blocks | MFCD00002747 | 256.430 | C16H32O2 | 98.000 | CCCCCCCCCCCCCCCC(O)=O | 100g | 290701204
Hexadecanoic acid | Combi-Blocks | 57-10-3 | MFCD00002747 | 256.430 | C16H32O2 | 98.000 | CCCCCCCCCCCCCCCC(O)=O | 100g | 290701204
eMolecules 57-10-3 | Hexadecanoic acid | Combi-Blocks | MFCD00002747 | 256.430 | C16H32O2 | 98.000 | CCCCCCCCCCCCCCCC(O)=O | 500g | 335346395
Hexadecanoic acid | Combi-Blocks | 57-10-3 | MFCD00002747 | 256.430 | C16H32O2 | 98.000 | CCCCCCCCCCCCCCCC(O)=O | 500g | 335346395
eMolecules 57-10-3 | Hexadecanoic acid | Combi-Blocks | MFCD00002747 | 256.430 | C16H32O2 | 98.000 | CCCCCCCCCCCCCCCC(O)=O | 5g | 335346394
Hexadecanoic acid | Combi-Blocks | 57-10-3 | MFCD00002747 | 256.430 | C16H32O2 | 98.000 | CCCCCCCCCCCCCCCC(O)=O | 5g | 335346394
Selleck Chemical LLC 3-Hydroxyisovaleric acid
3-Hydroxyisovaleric acid is a normal human metabolite excreted in the urine
Medchemexpress LLC 3-Methylvaleric acid (Standard) | 105-43-1 | 682090 | 99.5% | 116.16 | 50 MG
3-Methylvaleric acid (Standard) is an analytical standard form of 3-Methylvaleric acid (HY-W010513) intended for research and analytical applications. It is a branched alkanoic acid that can be utilized by *Pseudomonas citronettotis* as a sole carbon source for its growth. Its derivatives exhibit anti-hyperalgesic and anticonvulsant activities. This compound is of analytical standard grade, commonly used in qualitative, quantitative, and methodological research experiments in HPLC, GC, and MS.
- Analytical standard grade.
- Can be utilized by *Pseudomonas citronettotis* as a sole carbon source.
- Derivatives exhibit anti-hyperalgesic and anticonvulsant activities.
- Commonly used in qualitative, quantitative, and methodological research experiments in HPLC, GC, and MS.
Cambridge Isotope Laboratories Hexanoic acid (methyl-D3 98%) 0 1 g
Hexanoic acid (methyl-D3 98%) 0 1 g
Medchemexpress LLC 10-Undecenoic acid (stabilized with TBC) | 112-38-9 | 99.99% | 1 ML
10-Undecenoic acid, also known as Undecylenic acid, is recognized as an antifungal and neuroprotective agent. It demonstrates various biological activities including the inhibition of Aβ oligomerization, scavenging of Reactive Oxygen Species (ROS), and suppression of μ-calpain activity. It is also noted for its anticancer effects on diverse tumor types.
- Inhibits C. albicans biofilm formation
- Suppresses quorum sensing signals in Bacillus subtilis and Pseudomonas aeruginosa
- Induces apoptosis in tumor cells
- Shows dose-dependent cytotoxicity to human tumor cell lines
- Significantly increases expression and activity of alkaline phosphatase and calcium deposition
- Reduces cell death induced by H2O2
- Effectively clears MRSA infections