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M3664

Sigma-Aldrich

12-Methyltetradecanoic acid

Synonyme(s) :

(+)-12-Methyl myristic acid

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About This Item

Formule empirique (notation de Hill):
C15H30O2
Numéro CAS:
5502-94-3
Poids moléculaire :
242.40
Numéro MDL:
MFCD00083664
Code UNSPSC :
12352211
ID de substance PubChem :
24896866
Nomenclature NACRES :
NA.25

Pureté

≥98% (GC)

Groupe fonctionnel

carboxylic acid

Type de lipide

saturated FAs

Conditions d'expédition

ambient

Température de stockage

2-8°C

Chaîne SMILES 

CCC(C)CCCCCCCCCCC(O)=O

InChI

1S/C15H30O2/c1-3-14(2)12-10-8-6-4-5-7-9-11-13-15(16)17/h14H,3-13H2,1-2H3,(H,16,17)

Clé InChI

XKLJLHAPJBUBNL-UHFFFAOYSA-N

Actions biochimiques/physiologiques

12-Methyltetradecanoic acid (12-methylmyristic acid) is an anteiso-C(15)-fatty acid used in studies on the properties and functions of medium-chain anteiso-fatty acids. 12-methyltetradecanoic acid is studied to understand its antibacterial properties. 12-methyltetradecanoic acid represses the extracellular production of surfactants required for swarming motility in Pseudomonas aeruginosa PAO1.

Pictogrammes

Exclamation mark
GHS07

Mention d'avertissement

Warning

Mentions de danger

H315,H319,H335

Classification des risques

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

Organes cibles

Respiratory system

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

dust mask type N95 (US), Eyeshields, Gloves

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Kenneth C Wright et al.
Journal of experimental therapeutics & oncology, 5(1), 55-68 (2006-01-19)
The purpose of this research was to evaluate the effects of targeted arterial delivery of the branched chain fatty acid 12-methyltetradecanoic acid (12-MTA) on the VX2 squamous cell carcinoma in rabbits. An intramuscular VX2 squamous cell carcinoma was induced at
T Kitahara et al.
Bioscience, biotechnology, and biochemistry, 59(1), 78-82 (1995-01-01)
Both the enantiomers of aseanostatin P5 (sarcinic acid), an inhibitor of myeloperoxidase (MPO) release from human polymorphonuclear leukocytes (PMN), with high optical purity were synthesized by starting from (S)-2-methylbutanol and methyl (S)-3-hydroxy-2-methylpropanoate. They were converted to four diastereomers of aggreceride
Ying Xu et al.
Marine biotechnology (New York, N.Y.), 11(4), 495-504 (2008-11-26)
Eleven strains of Streptomyces isolated from deep-sea sediments were screened for anti-larval settlement activity and all were active. Among those strains, Streptomyces sp. UST040711-290 was chosen for the isolation of bioactive antifouling compounds through bioassay-guided isolation procedure. A branched-chain fatty
M R Edgcomb et al.
Biochimica et biophysica acta, 1463(1), 31-42 (2000-01-13)
Listeria monocytogenes is a foodborne psychrotrophic pathogen that grows at refrigeration temperatures. Previous studies of fatty acid profiles of wild-type and cold-sensitive, branched-chain fatty acid deficient mutants of L. monocytogenes suggest that the fatty acid 12-methyltetradecanoic (anteiso-C(15:0)) plays a critical
Ana Valéria Colnaghi Simionato et al.
Journal of mass spectrometry : JMS, 42(4), 490-496 (2007-02-14)
Xylella fastidiosa (X.f.) is a plant pathogen with high levels of genomic similarity to Xanthomonas campestris pv. campestris (X.c.c.). It has been shown that X. fastidiosa synthesizes a putative diffusible signal factor (X.f.-DSF) that activates regulation of pathogenicity factor (rpf)
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