Palmitic Acid

Palmitic Acid structural formula

CAS Number57-10-3
Molecular FormulaC16H32O2
Molecular Weight256.430
InChI KeyIPCSVZSSVZVIGE-UHFFFAOYSA-N
LogP7.17
Synonyms
  • Hexadecanoic acid
  • 57-10-3
  • Palmitic acid
  • 4-02-00-01157
  • 1-Pentadecanecarboxylic acid
  • Acide palmitique
  • acido palmitico, puro
  • Cetylic acid
  • Emersol 143
  • Hydrofol Acid 1690
  • Hystrene 9016
  • Kortacid 1695
  • Kortacid 1698
  • Loxiol EP 278
  • Lunac P 95KC
  • n-Hexadecanoic acid
  • n-Hexadecoic acid
  • NSC 5030
  • Palmitinic acid
  • PALMITINSAEURE
  • Palmitinsaure
  • Pentadecanecarboxylic acid
  • Prifac 2960
  • Pristerene 4934
  • BRN 0607489
  • EINECS 200-312-9
  • FEMA No. 2832
  • Palmitic acid 95%
  • UNII-2V16EO95H1
  • 1-hexyldecanoic acid
  • 16:00
  • C16
  • C16 fatty acid
  • C16:0
  • CH3-[CH2]14-COOH
  • Edenor C16
  • Emersol 140
  • Glycon P-45
  • Hexadecanoate
  • Hexadecanoic acid
  • Hexadecanoic acid palmitic acid
  • Hexadecoate
  • Hexadecylic acid
  • Hexaectylic acid
  • Hydrofol
  • Hystrene 8016
  • Industrene 4516
  • Lunac P 95
  • Lunac P 98
  • N-Hexadecanoate
  • N-Hexadecoate
  • PAM
  • PLM
  • Palmitate
  • Palmitinate
  • Palmitoate
  • Palmitoic acid
  • Pentadecanecarboxylate
  • Prifrac 2960
  • Univol U332
  • hexadecoic acid
  • 116860-99-2
  • 212625-86-0
  • 60605-23-4
  • 66321-94-6

Applications:

HPLC Analysis of Fatty Acids with MS Compatible Conditions

June 4, 2011


Fatty acids are carboxylic acids with a long unbranched carbon chain. They are hydrophobic compounds with different number of carbons. Most naturally occurring fatty acids have a chain of an even number of carbon atoms. Three fatty acids are separated on a Primesep 100 HPLC column by reversed-phase mechanisms. This general HPLC method and mixed-mode column can be used for separation of other fatty acids.

Application Column

Primesep 100

The Primesep family of mixed-mode columns offers a wide variety of stationary phases, boasting unprecedented selectivity in the separation of a broad array of chemical compounds across multiple applications. Corresponding Primesep guard columns, available with all stationary phases, do not require holders. SIELC provides a method development service available to all customers. Inquire about our specially-tailored custom LC-phases for specific separations.

Select options
Application Analytes:
Myristic Acid
Palmitic Acid
Stearic Acid

Application Detection:
ELSD Detection
SIELC Technologies usually develops more than one method for each compound. Therefore, this particular method may not be the best available method from our portfolio for your specific application. Before you decide to implement this method in your research, please send us an email to research@sielc.com so we can ensure you get optimal results for your compound/s of interest.