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W349003

Sigma-Aldrich

Ethyl stearate

≥97%

Synonym(s):

Ethyl octadecanoate, Stearic acid ethyl ester

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About This Item

Linear Formula:
CH3(CH2)16COOC2H5
CAS Number:
111-61-5
Molecular Weight:
312.53
FEMA Number:
3490
Beilstein:
1788183
EC Number:
203-887-4
Council of Europe no.:
745
MDL number:
MFCD00009006
UNSPSC Code:
12164502
PubChem Substance ID:
24901733
Flavis number:
9.210
NACRES:
NA.21
Organoleptic:
waxy
biological source:
synthetic
food allergen:
no known allergens, no known allergens
Pricing and availability is not currently available.

biological source

synthetic

Quality Level

400

Assay

≥97%

bp

213-215 °C/15 mmHg (lit.)

mp

34-38 °C (lit.)

application(s)

flavors and fragrances

Documentation

see Safety & Documentation for available documents

food allergen

no known allergens, no known allergens

Organoleptic

waxy

SMILES string

CCCCCCCCCCCCCCCCCC(=O)OCC

InChI

1S/C20H40O2/c1-3-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20(21)22-4-2/h3-19H2,1-2H3

InChI key

MVLVMROFTAUDAG-UHFFFAOYSA-N

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General description

Ethyl stearate is a fatty acid ethyl ester (FAEE) is commonly found in vegetable oils.[1][2]

Disclaimer

For R&D or non-EU Food use. Not for retail sale.

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

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

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Certificates of Analysis (COA)

Lot/Batch Number
SHBQ2775
SHBP8904
SHBL3755
MKCD0921
MKBZ9750V

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Kubickova I, et al.
Catalysis Today, 106(1), 197-200 (2005)
Comparison of ethyl glucuronide and fatty acid ethyl ester concentrations in hair of alcoholics, social drinkers and teetotallers.
Yegles M, et al.
Forensic Science International, 145(2), 167-173 (2004)
The dual role of macrophages in the sporozoite-induced malaria infection. A hypothesis.
J P Verhave et al.
International journal of nuclear medicine and biology, 7(2), 149-156 (1980-01-01)
S Aliaskarisohi et al.
The journal of physical chemistry. B, 115(40), 11631-11637 (2011-08-31)
In a previous work, Muruganathan and Fischer observed laser-induced local collapse of a methyl stearate monolayer. These experiments opened the possibility of studying the collapse mechanism in a highly controlled manner, since the laser intensity can be easily varied and
Yan-Bing Zhang et al.
Journal of Asian natural products research, 8(1-2), 119-123 (2006-06-07)
A new phenolic glycoside (1), mahkoside A, together with six known compounds including mangiferin (2), kaempferol-3-O-beta-D-glucoside (3), dodecanoic acid (4), palmitic acid (5) ethyl stearate (6) and sucrose (7), were isolated from the pit of Mahkota dewa. Their structures were
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