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Dihomo-?-Linolenic Acid-d6

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    Dihomo-?-Linolenic Acid-d<sub>6</sub>
  • Dihomo-?-Linolenic Acid-d<sub>6</sub>
Cat No: 10458
Biochemicals - Isotopically Labeled Standards
Cayman

Dihomo-γ-Linolenic Acid-d6 (DGLA-d6) contains six deuterium atoms at the 8, 9, 11, 12, 14, and 15 positions. It is intended for use as an internal standard for the quantification of DGLA by GC- or LC-mass spectrometry. Dihomo-γ-Linolenic Acid (DGLA, 2...

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Territorial Availability: Available through Bertin Technologies only in France
Synonyms:
  • 8Z,11Z,14Z-eicosatrienoic-8,9,11,12,14,15-d6 acid
Correlated keywords:
  • deuterated LC/MS GC-MS LC-MS mass spectrometry polyunsaturated dihomo-g-linolenic dihomo-?-linolenic dihomo-gamma-linolenic omega-6 ?-6 fatty acids antagonists arachidonic receptors LTB4 deuterium
Product Overview:
Dihomo-γ-Linolenic Acid-d6 (DGLA-d6) contains six deuterium atoms at the 8, 9, 11, 12, 14, and 15 positions. It is intended for use as an internal standard for the quantification of DGLA by GC- or LC-mass spectrometry. Dihomo-γ-Linolenic Acid (DGLA, 20:3), an elongation product of γ-linolenic acid (18:3), is rapidly metabolized by fatty acid desaturases to produce arachidonic acid (20:4). DGLA is metabolized through the cyclooxygenase pathway to produce 1-series prostaglandins, (PGs), including PGE1.{2244,10906} In mice, DGLA supplementation in the diet can reduce atopic dermatitis and atherosclerosis.{19739,19738}
Size 100 µg
Shipping dry ice
CAS Number 81540-86-5
Molecular Formula C20H28D6O2
SMILES [2H]/C(CCCCCCC(O)=O)=C([2H])/C/C([2H])=C([2H])\C/C([2H])=C([2H])\CCCCC
Molecular Weight 312,5
Formulation A solution in methyl acetate
Purity ≥99% deuterated forms (d1-d6)
Custom Code 3822.19
UNSPSC code 12352100

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Our scientists are experts in the synthesis, purification, and characterization of biochemicals ranging from small drug-like heterocycles to complex biolipids, fatty acids, and many others. We are also highly skilled in all aspects of assay and antibody development, protein expression, crystallization, and structure determination.

Over the past thirty years, Cayman developed a deep knowledge base in lipid biochemistry, including research involving the arachidonic acid cascade, inositol phosphates, and cannabinoids. This knowledge enabled the production of reagents of exceptional quality for cancer, oxidative injury, epigenetics, neuroscience, inflammation, metabolism, and many additional lines of research.

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