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O5505

Sigma-Aldrich

Stearyl oleate

~99%

Synonym(s):

Oleic acid stearyl ester

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About This Item

Empirical Formula (Hill Notation):
C36H70O2
CAS Number:
17673-49-3
Molecular Weight:
534.94
EC Number:
241-651-2
MDL number:
MFCD00056227
UNSPSC Code:
12352211
PubChem Substance ID:
24898022

assay

~99%

functional group

ester

shipped in

ambient

storage temp.

−20°C

SMILES string

CCCCCCCCCCCCCCCCCCOC(=O)CCCCCCC\C=C/CCCCCCCC

InChI

1S/C36H70O2/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-31-33-35-38-36(37)34-32-30-28-26-24-22-20-18-16-14-12-10-8-6-4-2/h18,20H,3-17,19,21-35H2,1-2H3/b20-18-

InChI key

WRPMUZXHQKAAIC-ZZEZOPTASA-N

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Packaging

Sealed ampule.

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

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 E Stewart et al.
Lipids, 16(5), 355-359 (1981-05-01)
Chromatography of stearyl oleate and cholesteryl oleate on thin layer plates coated with magnesium hydroxide-celite, 1:1, or magnesia-celite, 1:1, showed that magnesium hydroxide had better resolving power for the separation of these wax ester and steryl ester model compounds than
Jianzhong Chen et al.
Lipids, 51(11), 1269-1287 (2016-10-25)
Wax esters (WE) are one of the predominant lipid types in human meibomian gland secretions (meibum) and account for 40-50 % of total meibum lipids. Recently, we managed to quantify 51 isomeric groups of intact WE in normal human meibum samples
Andrey B Imbs et al.
PloS one, 14(4), e0215759-e0215759 (2019-04-30)
To expand our knowledge of lipid and fatty acid (FA) biosynthesis in marine cnidarians, polar lipidomes of hydrocorals were studied for the first time and then compared with those of soft corals from tropical and boreal regions. The structure and
Jianzhong Chen et al.
Lipids, 50(8), 821-836 (2015-07-17)
A series of different types of wax esters (represented by RCOOR') were systematically studied by using electrospray ionization (ESI) collision-induced dissociation tandem mass spectrometry (MS/MS) along with pseudo MS(3) (in-source dissociation combined with MS/MS) on a quadrupole time-of-flight (Q-TOF) mass

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