Menthoglycol

Base Information Edit

Chemical Name:Menthoglycol
CAS No.:3564-98-5
Deprecated CAS:81176-88-7
Molecular Formula:C₁₀H₂₀O₂
Molecular Weight:172.268
Hs Code.:2906199090
European Community (EC) Number:622-019-9
UNII:AAL436QJ5W,EB999AF32A
DSSTox Substance ID:DTXSID5035084,DTXSID801033610
Nikkaji Number:J451.638I
Wikidata:Q27088421
Pharos Ligand ID:A1QR87AGUNLC
Metabolomics Workbench ID:28151
Mol file:3564-98-5.mol

Synonyms:Menthoglycol;3564-98-5;trans-p-Menthane-3,8-diol;Isopulegol hydrate;(1R,2R,5R)-2-(2-hydroxypropan-2-yl)-5-methylcyclohexan-1-ol;(-)-3,8-p-Menthanediol;PMD38;(1R,3R,4R)-p-menthane-3,8-diol;p-MENTHANE-3,8-DIOL, cis-1,3,trans-1,4-;91739-72-9;(+-)-Isopulegol hydrate;UNII-AAL436QJ5W;EPA Pesticide Chemical Code 011550;AAL436QJ5W;UNII-EB999AF32A;1beta,3beta,4alpha-p-menthane-3,8-diol;EB999AF32A;(+/-)-trans-p-Menthane-3,8-diol;(1R,2R,5R)-2-(1-hydroxy-1-methylethyl)-5-methylcyclohexanol;(1R,3R,4R)-2-hydroxy-alpha,alpha,4-trimethylcyclohexanemethanol;Cyclohexanemethanol, 2-hydroxy-.alpha.,.alpha.,4-trimethyl-, (1R,2R,4R)-;Cyclohexanemethanol, 2-hydroxy-alpha,alpha,4-trimethyl-, (1-alpha,2-beta,4-beta)-;PMD;8-hydroxymenthol;(1R,2R,5R)-2-(2-hydroxypropan-2-yl)-5-methylcyclohexanol;Cyclohexanemethanol, 2-hydroxy-alpha,alpha,4-trimethyl-, (1R,2R,4R)-;Cyclohexanemethanol, 2-hydroxy-alpha,alpha,4-trimethyl-, (1R,2R,4E)-rel-;( -)-Isopulegol hydrate;trans-2-(2-Hydroxypropan-2-yl)-5-methylcyclohexanol;D03NZW;1,4-menthane-3,8-diol;SCHEMBL80732;GTPL2472;Cyclohexanemethanol, 2-hydroxy-.alpha.,.alpha.,4-trimethyl-, (1R,2R,4E)-;DTXSID5035084;CHEBI:16053;MENTHOGLYCOL, (+/-)-;DTXSID801033610;(+/-)-ISOPULEGOL HYDRATE;Cyclohexanemethanol, 2-hydroxy-.alpha.,.alpha.,4-trimethyl-, (1-.alpha.,2-.beta.,4-.beta.)-;MFCD00191552;AKOS037646772;3,8-P-MENTHANEDIOL, (-)-;LMPR0102090063;AS-70737;LS-89494;1beta,3beta,4alpha--p-menthane-3,8-diol;TRANS-P-MENTHANE-3,8-DIOL 95+%;1beta,3beta,4alpha-para-menthane-3,8-diol;p-Menthane-3,8-diol (cis-1,3,trans-1,4);C02904;Q27088421;2-(1-hydroxy-1-methyl-ethyl)-5-methyl-cyclohexan-1-ol;(1R,2R,4R)-2-Hydroxy-alpha,alpha,4-trimethylcyclohexanemethanol;Cyclohexanemethanol, 2-hydroxy-a,a,4-trimethyl-, (1R,2R,4R)-;cyclohexanemethanol, 2-hydroxy-alpha,alpha,4-trimethyl-, (1R,2R, 4E)-rel;rel-(1R,2R,4R)-2-Hydroxy-alpha,alpha,4-trimethylcyclohexanemethanol;CYCLOHEXANEMETHANOL, 2-HYDROXY-.ALPHA.,.ALPHA.,4-TRIMETHYL-, (1R,2R,4R)-REL-;cyclohexanemethanol, 2-hydroxy-alpha,alpha,4-trimethyl-, (1- alpha,2-beta,4-beta);CYCLOHEXANEMETHANOL, 2-HYDROXY-.ALPHA.,.ALPHA.,4-TRIMETHYL-, (1.ALPHA.,2.BETA.,4.BETA.)-;CYCLOHEXANEMETHANOL, 2-HYDROXY-.ALPHA.,.ALPHA.,4-TRIMETHYL-, (1R-(1.ALPHA.,2.BETA.,4.BETA.))-

Suppliers and Price of Menthoglycol

Supply Marketing:Edit

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Crysdot
trans-2-(2-Hydroxypropan-2-yl)-5-methylcyclohexanol 95+%
250mg
$ 352.00

Crysdot
trans-2-(2-Hydroxypropan-2-yl)-5-methylcyclohexanol 95+%
1g
$ 880.00

Chemenu
trans-2-(2-Hydroxypropan-2-yl)-5-methylcyclohexanol 95%
1g
$ 823.00

Total 13 raw suppliers

Chemical Property of Menthoglycol Edit

Chemical Property:

Melting Point:78°C
Boiling Point:267.6°Cat760mmHg
Flash Point:120.7°C
PSA：40.46000
Density:1.009g/cm³
LogP:1.55440
XLogP3:2.2
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:1
Exact Mass:172.146329876
Heavy Atom Count:12
Complexity:154

Purity/Quality:

100% ^*data from raw suppliers

trans-2-(2-Hydroxypropan-2-yl)-5-methylcyclohexanol 95+% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:
Safety Statements: 24/25

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1CCC(C(C1)O)C(C)(C)O
Isomeric SMILES:C[C@@H]1CC[C@H]([C@@H](C1)O)C(C)(C)O
Uses Menthoglycol is used in the making of insect repellant compositions. A mosquito repellents from leaves of Eucalyptus.

Technology Process of Menthoglycol

There total 15 articles about Menthoglycol which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 90.0%