Product Detail
Myo-Inositol-d6
Inositol Stable Isotope Reagent
Stock Status: Enquire
Live
For Research & Analytical Purposes. Not for Personal use.
Category
Stable Isotope Reagent
API Family
Inositol
Storage
Refer MSDS for complete information.
Hazard Information
Refer MSDS for complete information.
Myo-Inositol-d6 Product Information
Myo-Inositol-d6 is listed under Stable Isotope Reagent. It is associated with Inositol and is intended for analytical research, quality control and pharmaceutical reference standard applications. The product is supplied by Clearsynth under CAT No. CS-T-103453.
Clearsynth provides this compound for research and analytical use, with product information including CAS number, molecular formula, molecular weight, stock enquiry details and supporting documentation.
Technical Data
Product Name
Myo-Inositol-d6
CAS No.
87-89-8(unlabelled)
CAT No.
CS-T-103453
Molecular Formula
C6H6D6O6
Molecular Weight
186.19
Category
API Family
Storage Condition
Refer MSDS for complete information.
SMILES
[2H]O[C@@H]1[C@H](O[2H])[C@@H](O[2H])[C@H](O[2H])[C@@H](O[2H])[C@@H]1O[2H]
IUPAC Name
(1R,2R,3S,4R)-cyclohexane-1,2,3,4,5,6-hexaol; d6
Hazard Compound
Refer MSDS for complete information.
Description
Overview
myo-Inositol-d6 is an intermediate in the synthesis of scyllo-Inositol-d6 (I666053), the labeled analogue of scyllo-Inositol (I666050), a cyclohexanehexol derivative used in the treatment of amyotrophic lateral sclerosis.
Synonyms
Cyclohexitol-d6; Dambose-d6; Inosital-d6; Inosite-d6; Inositene-d6; Inositina-d6; Inositol-d6; MI; Mesoinosit-d6; Mesoinosite-d6; Mesoinositol-d6; Mesol-d6; Mesovit-d6; Myoinosite-d6; Nucite-d6; Phaseomannite-d6; Phaseomannitol-d6; Scyllite-d6; cis-1,2,3,5-trans-4,6-Cyclohexanehexol-d6; i-Inositol-d6;
Application Notes
myo-Inositol-d6 is an intermediate in the synthesis of scyllo-Inositol-d6 (I666053), the labeled analogue of scyllo-Inositol (I666050), a cyclohexanehexol derivative used in the treatment of amyotrophic lateral sclerosis.
References
Chishti, M., et al.: J. Biol. Chem., 276, 21562 (2001); Fisher, S., et al.: J. Neurochem., 82, 736 (2002); McLaurin, J., et al.: Nat. Med., 12, 801 (2006); Fenili, D., et al.: J. Mol. Med., 85, 603 (2007)
