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Informacje o tej pozycji
Wzór empiryczny (zapis Hilla):
C15H30O2
Numer CAS:
Masa cząsteczkowa:
242.40
UNSPSC Code:
12352211
PubChem Substance ID:
MDL number:
Pomoc techniczna
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Pozwól nam pomócassay
≥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.
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signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Klasa składowania
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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Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.
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
