Bornesitol
{{Chembox
| Watchedfields = changed
| verifiedrevid = 443426693
| ImageFile = Bornesitol.svg
| ImageSize = 150px
| IUPACName = 1D-1-O-Methyl-myo-inositol
| SystematicName = (1R,2R,3S,4S,5R,6S)-6-Methoxycyclohexane-1,2,3,4,5-pentol
| OtherNames = D-(−)-Bornesitol
|Section1={{Chembox Identifiers
| CASNo = 484-71-9
| CASNo_Ref = {{cascite|correct|CAS}}
| UNII_Ref = {{fdacite|correct|FDA}}
| UNII = RW8AP5YP8U
| PubChem = 440078
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
| ChemSpiderID = 10254649
| ChEBI_Ref = {{ebicite|correct|EBI}}
| ChEBI = 18427
| KEGG = C03659
| SMILES = O[C@@H]1[C@@H](O)[C@@H](O)[C@@H](OC)[C@H](O)[C@H]1O
| StdInChI_Ref = {{stdinchicite|correct|chemspider}}
| StdInChI=1S/C7H14O6/c1-13-7-5(11)3(9)2(8)4(10)6(7)12/h2-12H,1H3/t2-,3-,4+,5-,6-,7-/m1/s1
| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}}
| StdInChIKey = DSCFFEYYQKSRSV-AGZHHQKVSA-N
}}
|Section2={{Chembox Properties
| C=7 | H=14 | O=6
| Appearance =
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|Section3={{Chembox Hazards
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Bornesitol is a cyclitol. It can be found in the gentianaceae and menyanthaceae plant families.{{cite journal | doi = 10.1016/S0031-9422(00)94463-7 | title = Distribution of l-(+)-bornesitol in the gentianaceae and menyanthaceae | author = Norbert Schilling | journal = Phytochemistry | volume = 15 | issue = 5 | year = 1976 | pages = 824–826| bibcode = 1976PChem..15..824S }}{{dead link|date=March 2019|bot=medic}}{{cbignore|bot=medic}} Chemically, it is a methyl ether of D-myo-inositol.