Vinyl Palmitate (stabilized with MEHQ), with CAS number 693-38-9, is a chemical compound widely used as a building block in various chemical reactions. It is a versatile reagent that contains a vinyl group and a long hydrocarbon chain, making it suitable for organic synthesis applications. In the laboratory, this compound plays a crucial role in the development of polymers, esters, and other high-reactivity compounds. Its chemical structure allows it to participate in a range of reactions, including polymerization and esterification, depending on the conditions and reagents used.
The key properties that make Vinyl Palmitate a preferred choice include its chemical stability and reactivity with various reagents such as acids, bases, and catalysts. The stabilization with MEHQ ensures that the compound remains effective over a longer period, reducing the risk of degradation during storage. This stability is essential for maintaining consistent results in laboratory experiments. Additionally, its compatibility with a wide range of chemical environments makes it a reliable option for researchers and industrial chemists.
In Indonesian laboratories, Vinyl Palmitate is commonly used in chemical research, pharmaceutical development, and the production of specialty chemicals. It is frequently found in research facilities and industrial settings where chemical synthesis and formulation are key processes. Its role in creating coatings, adhesives, and other chemical products highlights its importance in both academic and industrial applications.
TCI brochures (PDF)
- Human-Serum-Albumin Binding Agents for Improvement of Pharmacokinetics 2019-02-22 · p. 2
- Lipids 2025-12-17 · p. 13
- Monomers 2025-05-28 · p. 13
Related TCI products
- TCI L0090 2146-71-6 Vinyl Laurate (stabilized with MEHQ)
- TCI U0057 5299-57-0 Vinyl 10-Undecenoate (stabilized with MEHQ)
- TCI C0896 818-44-0 Vinyl n-Octanoate (stabilized with MEHQ)
- TCI P0739 115-83-3 Pentaerythritol Tetrastearate (contains palmitate)
- TCI P0651 110-34-9 Isobutyl Palmitate
- TCI P0649 111-06-8 Butyl Palmitate
- Chemical synthesis for the production of polymers and esters due to its reactivity and structural versatility.
- Pharmaceutical research for the development of organic compounds requiring high reactivity and stability.
- Formulation of coatings and adhesives where the vinyl group contributes to cross-linking and durability.
- Industrial chemical manufacturing for the creation of specialty chemicals with specific functional properties.
- Organic reaction testing where the compound serves as a reliable and consistent building block for various synthetic pathways.
From the TCI brochure
- Palmitoylation reagent for introducing a fatty acid to optimize pharmacokinetics
| Brand | TCI |
|---|---|
| CAS number | 693-38-9 |
| Molecular formula | — |
| Purity | — |
| Category | Chemistry > Building Blocks > Non-Heterocyclic Building Blocks |
| Pack sizes | Available in various quantities as per supplier specifications |
| Physical form | Liquid |
| Storage | Store in a cool, dry place away from light and incompatible materials |
Vinyl Palmitate should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to keep the compound in a sealed container to prevent exposure to air and moisture. Suitable storage containers include glass or high-density polyethylene (HDPE) bottles, which are resistant to chemical reactions and provide a barrier against contaminants. In laboratory settings, it is important to ensure proper ventilation and avoid contact with incompatible substances such as strong oxidizers or acids. Always follow standard safety protocols when handling this compound to maintain a safe and controlled environment.
References cited in the TCI brochure
- Sharon Myers. Acylation of Human Insulin With Palmitic Acid Extends the Time Action of Human Insulin in Diabetic Dogs Diabetes, 1997. doi:10.2337/diab.46.4.637
- Lotte B. Knudsen. Potent Derivatives of Glucagon-like Peptide-1 with Pharmacokinetic Properties Suitable for Once Daily Administration Journal of Medicinal Chemistry, 2000. doi:10.1021/jm9909645
- Sung‐Hyun Yang. Lipidation of Cysteine or Cysteine‐Containing Peptides Using the Thiol‐Ene Reaction (CLipPA) European Journal of Organic Chemistry, 2016. doi:10.1002/ejoc.201501375
Product Categories
- Biochemicals and ReagentsAlbumin Binding AgentsAlbumin Binding Modification Reagents
- Biochemicals and ReagentsBioconjugationAlbumin Binding Modification Reagents
- Biochemicals and ReagentsLipidsFatty Acyls
- Pharmaceutical Development and Drug Discovery ResearchAlbumin Binding AgentsAlbumin Binding Modification Reagents
- Pharmaceutical Development and Drug Discovery ResearchBioconjugationAlbumin Binding Modification Reagents
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