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H6639

Sigma-Aldrich

Methyl heptacosanoate

≥99%

Synonym(s):

Heptacosanoic acid methyl ester

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About This Item

Linear Formula:
CH3(CH2)25COOCH3
CAS Number:
55682-91-2
Molecular Weight:
424.74
Beilstein:
1801611
MDL number:
MFCD00057798
UNSPSC Code:
12352211
PubChem Substance ID:
24895752

Assay

≥99%

form

powder

functional group

ester

shipped in

ambient

storage temp.

2-8°C

SMILES string

CCCCCCCCCCCCCCCCCCCCCCCCCCC(=O)OC

InChI

1S/C28H56O2/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-24-25-26-27-28(29)30-2/h3-27H2,1-2H3

InChI key

SCVPLVIKFSVDDH-UHFFFAOYSA-N

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Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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M J Paik et al.
Journal of chromatography. B, Biomedical sciences and applications, 721(1), 3-11 (1999-02-23)
A sensitive method for very-long-chain fatty acid analysis was developed by gas chromatography-nitrogen-phosphorus detection by using cyanomethyl derivatization. Bromoacetonitrile as alkylating reagent was used to improve nitrogen phosphorus detection detectability of compounds containing non-nitrogen. The carboxyl group of very-long-chain fatty
R Aliya et al.
Pakistan journal of pharmaceutical sciences, 4(2), 103-111 (1991-07-01)
The green seaweed Codium iyengarii Bphirg., collected from the coast of Karachi, has been studied for its fatty acid composition. The acids were converted into methyl caters and identified by GC-MS, which revealed the presence of 11 saturated, 10 monoethenoic
Characterization and carbon metabolism in fungi pathogenic to Triatoma infestans, a chagas disease vector.
Juarez MP, Crespo R, Fernandez GC, et al.
J. Invert. Path., 76, 198-207 (2000)

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