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P6617

Sigma-Aldrich

Pristanic acid

≥97% (GC), ethanol solution

Synonyma:

2,6,10,14-Tetramethylpentadecanoic acid

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About This Item

Empirický vzorec (Hillův zápis):
C19H38O2
Číslo CAS:
1189-37-3
Molekulová hmotnost:
298.50
EC Number:
200-578-6
MDL number:
MFCD05664739
UNSPSC Code:
12352106
PubChem Substance ID:
329820250
NACRES:
NA.77

Název produktu

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

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.

pictograms

FlameExclamation mark
GHS02,GHS07

signalword

Danger

hcodes

H225,H319

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 2

Storage Class

3 - Flammable liquids

wgk_germany

WGK 2

flash_point_f

55.4 °F

flash_point_c

13 °C

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

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Osvědčení o analýze (COA)

Lot/Batch Number
0000343311
0000335727
SLCQ5703
SLCN4022
SLCM1895

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Elaidic acid ≥99.0% (GC)

Sigma-Aldrich

E4637

Elaidic acid

Erucic acid ≥99% (capillary GC)

Sigma-Aldrich

E3385

Erucic acid

Behenic acid analytical standard

Supelco

11909

Behenic acid

Erucic acid analytical standard

Supelco

45629

Erucic acid

Palmitoleic acid ≥98.5% (GC), liquid

Sigma-Aldrich

P9417

Palmitoleic acid

Paraffin oil puriss., meets analytical specification of Ph. Eur., BP, viscous liquid

Sigma-Aldrich

18512

Paraffin oil

Oleic acid ≥99% (GC)

Sigma-Aldrich

O1008

Oleic acid

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
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)
James A Mobley et al.
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 12(8), 775-783 (2003-08-15)
An enzyme previously identified as alpha-methylacyl-CoA racemase (AMACR) is overexpressed in high-grade prostatic intraepithelial neoplasia and in a majority (60-100%) of prostate cancers (CaPs) as compared with normal and benign hyperplastic lesions of the prostate, where it is minimally expressed.
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
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