(±)-?-Tocopherol Acetate-d3

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(±)-?-Tocopherol Acetate-d₃

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Cat No: 30081

Biochemicals - Isotopically Labeled Standards

(±)-α-Tocopherol acetate-d3 is intended for use as an internal standard for the quantification of (±)-α-tocopherol acetate (Item No. 28399) by GC- or LC-MS. (±)-α-Tocopherol acetate is an acetate form of (±)-α-tocopherol (Item No. 25985), a biological...

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Territorial Availability: Available through Bertin Technologies only in France

Synonyms:

(2R)-rel-3,4-dihydro-2,5,7,8-tetramethyl-2-[(4R,8R)-4,8,12-trimethyltridecyl]-2H-1-benzopyran-6-ol, 6-(acetate-d3)

Correlated keywords:

deuterated deuterium vitE IL1? IL4 IFN?

Product Overview:
(±)-α-Tocopherol acetate-d3 is intended for use as an internal standard for the quantification of (±)-α-tocopherol acetate (Item No. 28399) by GC- or LC-MS. (±)-α-Tocopherol acetate is an acetate form of (±)-α-tocopherol (Item No. 25985), a biologically active form of vitamin E. It prevents reductions in the percentage of embryos developing into blastocysts and the levels of glutathione (GSH), as well as prevents increases in oxidative stress, in zygotes from mice exposed to heat stress prior to mating when administered to dams prior to heat stress at a dose of 1 g/kg.{48558} (±)-α-Tocopherol acetate (>1,050 IU/kg in the diet) prevents body weight loss and prevents decreases in pulmonary dynamic compliance in mice exposed to sidestream cigarette smoke but not in sham exposure animals.{48559} However, it also increases the levels of IL-1β, IL-4, and IFN-γ in the bronchoalveolar lavage fluid (BALF) of sidestream cigarette smoke-exposed, but not sham exposure, mice.

Size	500 µg
Shipping	dry ice
Molecular Formula	C₃₁H₄₉D₃O₃
SMILES	CC1=C2C(CC[C@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)O2)=C(C)C(OC(C([2H])([2H])[2H])=O)=C1C
Molecular Weight	475,8
Formulation	An oil
Purity	≥99% deuterated forms (d1-d3)
Custom Code	3822.19
UNSPSC code	12352100

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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.