P6617
Pristanic acid
≥97% (GC), ethanol solution
别名:
2,6,10,14-四甲基十五烷酸
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关于此项目
经验公式（希尔记法）:
C19H38O2
化学文摘社编号:
分子量:
298.50
UNSPSC Code:
12352106
PubChem Substance ID:
NACRES:
NA.77
EC Number:
200-578-6
MDL number:
产品名称
降植烷酸 溶液, mixture of isomers, ethanol solution, ≥97% (GC)
SMILES string
CC(C)CCCC(C)CCCC(C)CCCC(C)C(O)=O
InChI key
PAHGJZDQXIOYTH-UHFFFAOYSA-N
InChI
1S/C19H38O2/c1-15(2)9-6-10-16(3)11-7-12-17(4)13-8-14-18(5)19(20)21/h15-18H,6-14H2,1-5H3,(H,20,21)
assay
≥97% (GC)
form
ethanol solution
storage temp.
−20°C
Quality Level
相关类别
Biochem/physiol Actions
饮食中脂肪酸（特别是植烷酸）的氧化产物。植烷酸通过α氧化反应进行氧化，生成降植烷酸，其随后通过过氧化物酶体β氧化降解。一些论文描述了一种或多种植烷酸或降植烷酸分解缺陷的一些先天代谢疾病。
signalword
Danger
hcodes
Hazard Classifications
Eye Irrit. 2 - Flam. Liq. 2
存储类别
3 - Flammable liquids
wgk
WGK 2
flash_point_f
55.4 °F
flash_point_c
13 °C
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
危险化学品
此项目有
S Ferdinandusse et al.
American journal of human genetics, 78(6), 1046-1052 (2006-05-11)
In this report, we describe the first known patient with a deficiency of sterol carrier protein X (SCPx), a peroxisomal enzyme with thiolase activity, which is required for the breakdown of branched-chain fatty acids. The patient presented with torticollis and
Antonella Peduto et al.
Molecular genetics and metabolism, 82(3), 224-230 (2004-07-06)
Peroxisomal disorders include a complex spectrum of diseases, characterized by a high heterogeneity from both the clinical and the biochemical points of view. Specific assays are required for the study of peroxisome metabolism. Among these, pipecolic acid evaluation is considered
D S Roe et al.
Molecular genetics and metabolism, 87(1), 40-47 (2005-11-22)
The differentiation of carnitine-acylcarnitine translocase deficiency (CACT) from carnitine palmitoyltransferase type II deficiency (CPT-II) and long-chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency from mitochondrial trifunctional protein deficiency (MTP) continues to be ambiguous using current acylcarnitine profiling techniques either from plasma or blood
R J Wanders et al.
European journal of pediatrics, 153(7 Suppl 1), S44-S48 (1994-01-01)
Peroxisomal disorders represent a recently recognized group of inherited diseases in man, now comprising 14 different disorders. If discussion is restricted to those peroxisomal disorders in which there is neurological involvement (thereby excluding hyperoxaluria and acatalasaemia), results over the least
Phytanic and pristanic acid are naturally occuring ligands.
Anna W M Zomer et al.
Advances in experimental medicine and biology, 544, 247-254 (2004-01-10)
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