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M7031

13-Methylmyristic acid

≥98% (capillary GC)

Synonym(e):

13-Methyltetradecanoic acid

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Über diesen Artikel

Empirische Formel (Hill-System):
C15H30O2
CAS-Nummer:
Molekulargewicht:
242.40
UNSPSC Code:
12352211
PubChem Substance ID:
MDL number:
Technischer Dienst
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assay

≥98% (capillary GC)

form

solid

functional group

carboxylic acid

shipped in

ambient

storage temp.

2-8°C

SMILES string

CC(C)CCCCCCCCCCCC(O)=O

InChI

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

InChI key

ZOCYQVNGROEVLU-UHFFFAOYSA-N

Biochem/physiol Actions

13-Methyltetradecanoic acid (13-Methylmyristic acid, 13-MTD, 13-MTDA), an iso-fatty acid, is used to study the induction of mitochondrial-mediated apoptosis via the AKT and MAPK pathways. 13-MTDA is used for the biosynthesis of methyl-branched polyhydroxyalkanoates.


pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Lagerklasse

11 - Combustible Solids

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves



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R A Klein et al.
Lipids, 15(8), 572-579 (1980-08-01)
We show in this paper that 13-methyltetradecanoic acid (13-MTD) can be used as a structually labeled marker for investigating the mobility of fatty acyl chains in adipose tissue in the rat. The presence of an omega-1 methyl group allows easy
Tianxin Lin et al.
Urologic oncology, 30(3), 339-345 (2010-09-17)
13-Methyltetradecanoic acid (13-MTD), a saturated branched-chain fatty acid purified from soy fermentation products, is known to induce apoptosis in many types of human cancer cells. This study was designed to investigate the molecular mechanisms involved in 13-MTD-induced apoptosis in human
Sawitree Wongtangtintharn et al.
Journal of nutritional science and vitaminology, 50(2), 137-143 (2004-07-10)
This paper describes the antitumoral activity of branched-chain fatty acid (BCFA) in human breast cancer cells with an emphasis on its effect on fatty acid biosynthesis. First, the relationship between chain-length and antitumoral activity was studied. The highest activity was