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85775

Sigma-Aldrich

Stearyl stearate

≥98.0% (GC)

Synonym(s):

Stearic acid stearyl ester

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About This Item

Linear Formula:
CH3(CH2)16COO(CH2)17CH3
CAS Number:
2778-96-3
Molecular Weight:
536.96
Beilstein/REAXYS Number:
1807499
EC Number:
220-476-5
MDL number:
MFCD00056225
UNSPSC Code:
12352211
PubChem Substance ID:
57653070
NACRES:
NA.25

biological source

synthetic

Quality Level

100

assay

≥98.0% (GC)

form

powder

functional group

ester

lipid type

saturated FAs

shipped in

ambient

storage temp.

2-8°C

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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Related Categories

Storage Class

11 - Combustible Solids

wgk_germany

nwg

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificates of Analysis (COA)

Lot/Batch Number
BCCM0066
BCCK1284
BCCH5151
BCCF0287
BCCC4251

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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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