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P6617

Pristanic acid

Name: Pristanic acid
Brand: SIGMA

≥97% (GC), ethanol solution

Synonym(s):

2,6,10,14-Tetramethylpentadecanoic acid

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About This Item

Empirical Formula (Hill Notation):

C₁₉H₃₈O₂

CAS Number:

1189-37-3

Molecular Weight:

298.50

UNSPSC Code:

12352106

PubChem Substance ID:

329820250

NACRES:

NA.77

EC Number:

200-578-6

MDL number:

MFCD05664739

Assay:

≥97% (GC)

Form:

ethanol solution

Quality level:

200

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Product Name

Pristanic acid solution, mixture of isomers, ethanol solution, ≥97% (GC)

Quality Level

200

assay

≥97% (GC)

form

ethanol solution

storage temp.

−20°C

SMILES string

CC(C)CCCC(C)CCCC(C)CCCC(C)C(O)=O

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)

InChI key

PAHGJZDQXIOYTH-UHFFFAOYSA-N

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Related Categories

Bioactive Small Molecules

Biochem/physiol Actions

Oxidation product of fatty acids in the diet, particularly phytanic acid. Phytanic acid is oxidized by alpha oxidation yielding pristanic acid, which is subsequently degraded by peroxisomal beta oxidation. Several inborn errors of metabolism with one or more deficiencies in the phytanic acid and pristanic acid breakdown have been described.

Disclaimer

Supply conditions do not apply to the regions and states of Brazil: North, Northeast, Mato Grosso do Sul, Mato Grosso, and Rio Grande do Sul.

pictograms

GHS02,GHS07

signalword

Danger

hcodes

H225,H319

pcodes

P210 - P233 - P240 - P241 - P242 - P305 + P351 + P338

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 2

Storage Class

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

Regulatory Information

危险化学品

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Certificates of Analysis (COA)

Lot/Batch Number

0000497891

0000495802

0000468872

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Mutations in the gene encoding peroxisomal sterol carrier protein X (SCPx) cause leukencephalopathy with dystonia and motor neuropathy.

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

Hyperpipecolic acidaemia: a diagnostic tool for peroxisomal disorders.

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

Clinical and biochemical characteristics of peroxisomal disorders: an update.

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)

Differentiation of long-chain fatty acid oxidation disorders using alternative precursors and acylcarnitine profiling in fibroblasts.

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

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Global Trade Item Number

SKU	GTIN
P6617-5MG	04061834393672

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