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Stearyl stearate

analytical standard

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Synonym(s):
Stearic acid stearyl ester
Linear Formula:
CH3(CH2)16COO(CH2)17CH3
CAS Number:
2778-96-3
Molecular Weight:
536.96
Beilstein:
1807499
EC Number:
220-476-5
MDL number:
MFCD00056225
UNSPSC Code:
85151701
PubChem Substance ID:
329757166
NACRES:
NA.24

grade

analytical standard

Quality Level

100

Assay

≥98% (GC)

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

format

neat

functional group

ester

storage temp.

room temp

SMILES string

CCCCCCCCCCCCCCCCCCOC(=O)CCCCCCCCCCCCCCCCC

InChI

1S/C36H72O2/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/h3-35H2,1-2H3

InChI key

NKBWPOSQERPBFI-UHFFFAOYSA-N

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General description

Stearyl stearate is the ester of stearic acid and 1-octadecanol.

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Stearyl stearate may be used as a model lipid to stain contact lenses in evaluating the lipid-degrading ability of the cholesterol esterase enzyme produced from Pseudomonas aeruginosa.

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WGK

nwg

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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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Purification and characterization of a novel cholesterol esterase from Pseudomonas aeruginosa, with its application to cleaning lipid-stained contact lenses.
Sugihara A.
Bioscience, Biotechnology, and Biochemistry, 66(11), 2347-2355 (2002)
Derivatisation using m-(trifluoromethyl) phenyltrimethylammonium hydroxide of organic materials in artworks for analysis by gas chromatography?mass spectrometry: unusual reaction products with alcohols.
Sutherland K.
Journal of Chromatography A, 1149(1), 30-37 (2007)
Dorothy M Duffy et al.
Langmuir : the ACS journal of surfaces and colloids, 20(18), 7630-7636 (2004-08-25)
Living organisms can control the size, shape, and structure of minerals. Attempts to reproduce this biological control in the laboratory often use Langmuir monolayers of long-chain carboxylic acids. We use large-scale molecular dynamics simulations to calculate the interfacial energies of
K Maeda et al.
Journal of chromatography, 221(2), 199-204 (1980-12-12)
A gas chromatographic--mass spectrometric analysis was used to separate and identify abnormal compounds in the nail of psoriatic patients. The nail was extracted with heated ethanol, and the extract was analyzed with and without trimethylsilylation. Tetradecanoic acid octadecyl ester, hexadecanoic

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