D-Pinitol Basic information
Product Name: |
D-Pinitol |
Synonyms: |
PINITOL;3-O-METHYL-D-CHIRO-INOSITOL;D-PINITOL;D-chiro-Inositol, 3-O-methyl-;D-PINTIOL;D-Pinitol 98.0%min;Pinit;D-Pinitol,95% |
CAS: |
10284-63-6 |
MF: |
C7H14O6 |
MW: |
194.18 |
EINECS: |
|
Product Categories: |
Miscellaneous Natural Products;chemical reagent;pharmaceutical intermediate;phytochemical;reference standards from Chinese medicinal herbs (TCM).;standardized herbal extract;reagent;standard substance;Miscellaneous |
Mol File: |
10284-63-6.mol |
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D-Pinitol Chemical Properties |
mp |
179-185 °C(lit.) |
alpha |
56 º (c=1, H2O) |
EPA Substance Registry System |
D-chiro-Inositol, 3-O-methyl-(10284-63-6) |
Hazard Codes |
F,C |
Risk Statements |
11-34 |
Safety Statements |
22-24/25-45-36/37/39-26-16 |
WGK Germany |
3
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Pinitol is a cyclitol, a cyclic polyol. It is a known anti-diabetic agent isolated from Sutherlandia frutescens leaves. Gall plant tannins can be differentiated by their content of pinitol. It was first identified in the sugar pine (Pinus lambertiana).
Certain variants of the bacteria Pseudomonas putida have been used in organic synthesis, the first example being the oxidation of benzene, employed by Steven Ley in the synthesis of (+/-)pinitol.
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