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(±)12(13)-EpOME-d4

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    (±)12(13)-EpOME-<wbr/>d<sub>4</sub>
  • (±)12(13)-EpOME-<wbr/>d<sub>4</sub>
Cat No: 10009996
Chemicals - Labeled Analytical Standards
Cayman
€119.00
Price is excluding VAT and does not include packaging neither shipping

Intended for use as an internal standard for the quantification of (±)12(13)-EpOME by GC- or LC-MS.
(±)12(13)-EpOME-d4 contains four deuterium atoms at the 9, 10, 12, and 13 positions. It is intended for use as an internal standard for the quantificati...

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Territorial Availability: Available through Bertin Technologies only in Europe
Product Overview:
Intended for use as an internal standard for the quantification of (±)12(13)-EpOME by GC- or LC-MS.
(±)12(13)-EpOME-d4 contains four deuterium atoms at the 9, 10, 12, and 13 positions. It is intended for use as an internal standard for the quantification of (±)12(13)-EpOME by GC- or LC-mass spectrometry (MS). (±)12(13)-EpOME is the 12,13-cis epoxide of linoleic acid, generated by neutrophils during the oxidative burst. The toxicity and biosynthesis of (±)12(13)-EpOME have not been well differentiated from (±)9(10)-EpOME (Item No. 52400), but have been presumed to be essentially the same. (±)9(10)-EpOME is generated by neutrophils during the oxidative burst. It has been recovered from the lungs of hyperoxic rats and from humans with acute respiratory distress syndrome.
Size: 25 µg
Shipping: wet ice
Stability: Store at -20 degrees; shelf life 365 days maximum after production
Molecular Formula: C18H28D4O3
SMILES: CCCCC[C@]1([2H])[C@](O1)([2H])C/C([2H])=C([2H])\CCCCCCCC(O)=O
Molecular Weight: 300.5
Formulation: A solution in methyl acetate
Purity: ≥99% deuterated forms (d1-d4)
Custom Code: 2916196000
UNSPSC code: 12352100
UN Number: UN1231

Cayman Chemical's mission is to help make research possible by supplying scientists worldwide with the basic research tools necessary for advancing human and animal health. Our utmost commitment to healthcare researchers is to offer the highest quality products with an affordable pricing policy.

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.

Our organic and analytical chemists specialize in the rapid development of manufacturing processes and analytical methods to carry out clinical and commercial GMP-API production. Pre-clinical drug discovery efforts are currently underway in the areas of bone restoration and repair, muscular dystrophy, oncology, and inflammation. A separate group of Ph.D.-level scientists are dedicated to offering Hit-to-Lead Discovery and Profiling Services for epigenetic targets. Our knowledgeable chemists can be contracted to perform complete sample analysis for analytes measured by the majority of our assays. We also offer a wide range of analytical services using LC-MS/MS, HPLC, GC, and many other techniques.

Accreditations
ISO/IEC 17025:2005
ISO Guide 34:2009

Cayman is a leader in the field of emerging drugs of abuse, providing high-purity Schedule I-V Controlled Substances to federally-licensed laboratories and qualified academic research institutions for forensic analyses. We are certified by ACLASS Accreditation Services with dual accreditation to ISO/IEC 17025:2005 and ISO Guide 34:2009.

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