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Key Documents

O7385

Sigma-Aldrich

4-Oxatetradecanoic acid

≥90% (GC)

Synonym(s):

3-(Decyloxy)propanoic acid

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About This Item

Empirical Formula (Hill Notation):
C13H26O3
CAS Number:
Molecular Weight:
230.34
MDL number:
UNSPSC Code:
12352211
PubChem Substance ID:
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Assay

≥90% (GC)

storage temp.

−20°C

SMILES string

CCCCCCCCCCOCCC(O)=O

Other Notes

Myristic acid analog.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

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

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C A Langner et al.
The Journal of biological chemistry, 267(24), 17159-17169 (1992-08-25)
Candida albicans and Cryptococcus neoformans are major causes of systemic fungal infections, particularly in patients with acquired immunodeficiency syndrome. Metabolic labeling studies revealed that these organisms synthesize a small number of N-myristoylproteins, the most prominent being 20-kDa ADP-ribosylation factors (Arfs).
Néstor M Carballeira et al.
Chemistry and physics of lipids, 136(1), 47-54 (2005-05-19)
The unprecedented (+/-)-2-methoxy-4-oxatetradecanoic acid and the optically pure (S)-2-methoxy-4-oxatetradecanoic acid were synthesized in six steps and in 11-14% overall yields starting with either 1,2-O-isopropylidene-rac-glycerol or 1,2-O-isopropylidene-(S)-glycerol. The key step in the synthesis was the selective monosilylation of a dibutylstannylene intermediate.

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