D-Mannitol

CHF 48.00
In stock
CDX-M0228-G500500 gCHF 48.00
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Product Details
Synonyms Mannite; Osmitrol; Cordycepic acid
Product Type Chemical
Properties
Formula C6H14O6
MW 182.17
CAS 69-65-8
Purity Chemicals ≥97% (HPLC)
Appearance White crystalline powder.
Solubility Soluble in water, alcohol or glycerol.
Identity Determined by NMR.
Declaration Manufactured by Chemodex.
Other Product Data

Click here for Original Manufacturer Product Datasheet
Our product description may differ slightly from the original manufacturers product datasheet.

InChi Key FBPFZTCFMRRESA-KVTDHHQDSA-N
Smiles OC[C@H]([C@H]([C@@H]([C@@H](CO)O)O)O)O
Shipping and Handling
Shipping AMBIENT
Short Term Storage +20°C
Long Term Storage +20°C
Handling Advice Protect from light and moisture.
Use/Stability Stable for at least 2 years after receipt when stored at +20°C.
Documents
MSDS Inquire
Product Specification Sheet
Datasheet Download PDF

Sugar alcohol that can be used as an inert osmotic control substance. The uptake and phosphorylation of D-Mannitol is catalyzed by the mannitol-specific phosphoenolpyruvate-dependent phosphotransferase systems (PTS). Used in pharmacy as excipient and diluent for solids and liquids and in analytical chemistry for boron determinations. It is used as an anticaking and free-flow agent, flavoring agent, lubricant and release agent, stabilizer and thickener and nutritive sweetener in the food industry. Used in sweetness inhibition studies. Can interact with neutrophils and monocytes. Experiments have shown that it is able to decrease neutrophil apoptosis in vitro. Can lower fat digestibility and body fat accumulation in rats, as well as upregulate monocyte HLA-DR, monocyte and neutrophil CD11b.

Product References

(1) Q. Wang, et al.; Drug Metab. Dispos. 36, 2244 (2008) | (2) M. Turina, et al.; Inflammation 31, 74 (2008) | (3) A. Nishiyama, et al.; J. Nutr. Sci. Vitaminol. 55, 242 (2009) | (4) B.C. Saha & F.M. Racine; Appl. Microbiol. Biotechnol. 89, 879 (2011) | (5) A. Kumar, et al.; J. Clin. Diagn. Res. 8, GE01 (2014) | (6) H.L. Ohrem, et al.; Pharm. Dev. Technol. 19, 257 (2014) | (7) P. Andre & F. Villain; Int. J. Cosmet. Sci. (2016)

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