Mometasone Furoate-d3

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Mometasone Furoate-d₃

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Cat No: 33470

Biochemicals - Isotopically Labeled Standards

Mometasone furoate-d3 is intended for use as an internal standard for the quantification of mometasone furoate (Item No. 21365) by GC- or LC-MS. Mometasone furoate is a prodrug form of the synthetic glucocorticoid mometasone (Item No. 31702).{33206} I...

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Territorial Availability: Available through Bertin Technologies only in France

Synonyms:

(8S,9R,10S,11S,13S,14S,16R,17R)-9-chloro-17-(2-chloroacetyl)-11-hydroxy-10,13,16-trimethyl-3-oxo-6,7,8,9,10,11,12,13,14,15,16,17-dodecahydro-3H-cyclopenta[a]phenanthren-17-yl furan-2-carboxylate-d3

Correlated keywords:

SCH 32088 SCH32088 deuterated deuterium GCMS LCMS Asmanex Twisthaler Ecural Elocom Elocon Elomet Monovo Nasonex Ovixan

Product Overview:
Mometasone furoate-d3 is intended for use as an internal standard for the quantification of mometasone furoate (Item No. 21365) by GC- or LC-MS. Mometasone furoate is a prodrug form of the synthetic glucocorticoid mometasone (Item No. 31702).{33206} Intranasal administration of mometasone furoate (1 µg/nostril) reduces the frequency of sneezing and nasal rubbing in a rat model of histamine-induced allergic rhinitis.{61270} Topical application of mometasone furoate reduces croton oil-induced ear edema in mice (ED50 = 0.31 µg/ml).{61271} Formulations containing mometasone furoate have been used in the treatment of allergic rhinitis, atopic dermatitis, and asthma.

Size	500 µg
Shipping	dry ice
Molecular Formula	C₂₇H₂₇Cl₂D₃O₆
SMILES	O=C1C=C[C@@]2(C)C(CC[C@]3([H])[C@]2(Cl)[C@@H](O)C[C@@]4(C)[C@@]3([H])C[C@@H](C)[C@]4(OC(C5=C([2H])C([2H])=C([2H])O5)=O)C(CCl)=O)=C1
Molecular Weight	524,5
Formulation	A solid
Purity	≥99% deuterated forms (d1-d3)
Custom Code	3822.19
UNSPSC code	12352100

Technical File

MSDS

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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.