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dinor-12-oxo Phytodienoic Acid-d5

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    dinor-<wbr/>12-<wbr/>oxo Phytodienoic Acid-<wbr/>d<sub>5</sub>
  • dinor-<wbr/>12-<wbr/>oxo Phytodienoic Acid-<wbr/>d<sub>5</sub>
Cat No: 10696
Biochemicals - Isotopically Labeled Standards
Price is excluding VAT and does not include packaging neither shipping

dinor-12-oxo Phytodienoic acid-d5 (dinor-OPDA-d5) contains five deuterium atoms at the 4, 4', 5, 5, and 5 positions. It is intended for use as an internal standard for the quantification of dinor-OPDA by GC- or LC-mass spectrometry (MS). In plants, ce...


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Territorial Availability: Available through Bertin Pharma only in Europe
  • 4-oxo-5S-(2Z)-2-penten-4,4,5,5,5-d5-1-yl-2-cyclopentene-1S-hexanoic acid
Correlated keywords:
  • jasmonates pathways plants hormones senescence development intermediates jasmonic acids glycerolipids galactolipids arabidopsides dnOPDA dn-OPDA deuterateds deuteriums LC-MS LC/MS GC-MS GC/MS mass spectrometry MS LC GC standards
Product Overview:
dinor-12-oxo Phytodienoic acid-d5 (dinor-OPDA-d5) contains five deuterium atoms at the 4, 4', 5, 5, and 5 positions. It is intended for use as an internal standard for the quantification of dinor-OPDA by GC- or LC-mass spectrometry (MS). In plants, certain unsaturated fatty acids are oxygenated and then further modified along the jasmonate pathway to produce plant hormones that are involved in senescence, flower development, mechanotransduction, and the response to herbivory.{18450} dinor-OPDA is an intermediate in the synthesis of jasmonic acid from hexadecatrienoic acid.{19252,19254} dinor-OPDA can also be incorporated into glycerolipids and galactolipids, including certain arabidopsides.{19253,19255}
Size 50 µg
Shipping dry ice
Stability Store at -80 degrees; shelf life 365 days
Molecular Formula C16H19D5O3
SMILES O=C1[C@@H](C/C=C\C([2H])([2H])C([2H])([2H])[2H])[C@@H](CCCCCC(O)=O)C=C1
Molecular Weight 269,4
Formulation A solution in methanol
Purity ≥99% deuterated forms (d1-d5)
Custom Code 2937.50
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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