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291781

Sigma-Aldrich

Isopropyl palmitate

technical grade, 90%

Synonym(s):

Isopropyl hexadecanoate

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About This Item

Linear Formula:
CH3(CH2)14COOCH(CH3)2
CAS Number:
142-91-6
Molecular Weight:
298.50
Beilstein:
1786567
EC Number:
205-571-1
MDL number:
MFCD00008993
UNSPSC Code:
12352100
PubChem Substance ID:
24857445
NACRES:
NA.22

grade

technical grade

Assay

90%

refractive index

n20/D 1.438 (lit.)

mp

11-13 °C (lit.)

density

0.852 g/mL at 25 °C (lit.)

SMILES string

CCCCCCCCCCCCCCCC(=O)OC(C)C

InChI

1S/C19H38O2/c1-4-5-6-7-8-9-10-11-12-13-14-15-16-17-19(20)21-18(2)3/h18H,4-17H2,1-3H3

InChI key

XUGNVMKQXJXZCD-UHFFFAOYSA-N

Gene Information

human ... CNR1(1268) , CNR2(1269)
rat ... Faah(29347)

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Application

Isopropyl palmitate has been used:
  • to formulate and evaluate the suitability of pluronic lecithin organogels containing flurbiprofen for topical application
  • to characterize microemulsion systems of isopropyl palmitate, water and 2:1 Brij 97, and 1-butanol by different experimental techniques

Storage Class Code

10 - Combustible liquids

WGK

nwg

Flash Point(F)

235.4 °F - closed cup

Flash Point(C)

113 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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M S Pandey et al.
Indian journal of pharmaceutical sciences, 71(1), 87-90 (2010-02-24)
The purpose of this research is to formulate and evaluate the suitability of pluronic lecithin organogels containing flurbiprofen for topical application. Four formulations were developed using flurbiprofen, lecithin, Pluronic F127, isopropyl palmitate, water, sorbic acid and potassium sorbate were coded
G Häring et al.
Biochemical and biophysical research communications, 127(3), 911-915 (1985-03-29)
A reverse micellar system containing Tween 85 and water in isopropylpalmitate was developed which permitted the solubilization of bacteria in the form of homogenous organic solutions. The presence of the bacteria in solution was demonstrated by light microscopy. Immediately after
Honglei Xi et al.
International journal of pharmaceutics, 436(1-2), 857-861 (2012-07-17)
The aim of this work was to investigate the effect of the stability of hydrogen-bonded ion pairs with organic amines on transdermal penetration of teriflunomide (TEF). Five organic amines, diethylamine (DEtA), triethylamine (TEtA), diethanolamine (DEA), triethanolamine (TEA), and N-(2'-hydroxyethanol)-piperdine (NP)
Varaporn Buraphacheep Junyaprasert et al.
Drug delivery, 15(5), 323-330 (2008-09-03)
The skin permeation enhancement of many kinds of drugs and cosmetic substances by microemulsions has been widely known; however, the correlations between microemulsion microstructures and the efficiency of skin permeation are not fully elucidated. Therefore, the aim of our study
P Boonme et al.
Die Pharmazie, 61(11), 927-932 (2006-12-13)
The aim of this work was to determine the type and microstructure of microemulsion samples formed in IPP/water/AerosolOT:1-butanol (2:1) systems as a case study for the investigation of microemulsions. The concentration of the surfactant/cosurfactant mixture was kept constant while the
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