homomenthol
3,3,5-trimethylcyclohexanol
 
Notes:
Menthol replacer. Flavouring ingredient
  • Lluch Essence
    • Lluch Essence S.L.
      A family company dedicated to sales and distribution
      Flexibility, availability, price and quality.
      Flexibility, availability, price and quality make LLUCH ESSENCE S.L. one of Europe’s references when it comes to essential oils and aroma chemicals, and it is now well known all around the world.
      Email: Info
      Voice: 34 93 379 38 49
      Fax: 34 93 370 65 04
      Linkedin
      Product(s):
      TRIMETHYLCYCLOHEXANOL MIX
       
  • Moellhausen
  • Penta International
    • Penta International Corporation
      Chemistry innovation
      At Penta, our products and services help businesses do business better.
      For over 30 years, Penta Manufacturing Company has played a growing role in worldwide chemistry innovations and applications. As an industry leader, Penta continues to pioneer chemistry-based solutions for practically every area of commerce. Our products and expertise have helped fuel technical advances in dozens of commercial applications including flavoring, coloring, fragrances and chemical processes.
      US Email: Technical Services
      US Email: Sales
      US Voice: (973) 740-2300
      US Fax: (973) 740-1839
      Product(s):
      20-79600 3,3,5-TRIMETHYLCYCLOHEXANOL
       
  • TCI AMERICA
    • TCI AMERICA
      Moving Your Chemistry Forward
      We continuously strive to advance our technology.
      With East & West Coast distribution centers, count on TCI to deliver products quickly and reliably. Over 28,000 Reagents available today in benchtop to bulk quantities. Sign up for a TCI account today for fast and free shipping!
      Tokyo Chemical Industry Co., Ltd. (TCI) is a leading worldwide manufacturer of specialty organic chemicals founded in 1946. TCI provides organic laboratory chemicals as well as pharmaceutical, cosmetic and functional materials. More than 60 years of synthesis experience and multi-purpose plants enable TCI to offer more than 28,000 products as well as custom synthesis. TCI has established overseas facilities in North America, Europe, China and India to serve customers worldwide.
      US Email: Sales
      Email: Technical Support
      Voice: 1-800-423-8616
      Fax: 1- 888-520-1075
      Facebook
      Twitter
      Instagram
      Linkedin
      RSS
      Product(s):
      T0472 3,3,5-Trimethylcyclohexanol (cis- and trans- mixture) >90.0%(GC)
       
  • Vigon International
    • Vigon International, Inc.
      Passion for Simplicity
      Manufacturer and supplier of high quality flavor and fragrance ingredients.
      The growth and success of Vigon is due in large part to a unique corporate concept that Vigon has developed and established within the industry: Creative Partnerships. This partnership concept has been and continues to be the foundation and guiding principle for all of Vigon's activities.
      US Email: Sales
      US Voice: 570-476-6300
      US Fax: 570-476-1110
      Facebook
      Twitter
      Linkedin
      Newsletter
      Blog
      Products List: View
      Product(s):
      501616 Trimethyl-3,3,5 Cyclohexanol (Homomenthol)
       
Synonyms   Articles   Notes   Search
CAS Number: 116-02-9Picture of molecule3D/inchi
ECHA EINECS - REACH Pre-Reg: 204-122-7
FDA UNII: 08CL3G94GH
Nikkaji Web: J46.555K
Beilstein Number: 2203314
MDL: MFCD00019378
XlogP3-AA: 2.60 (est)
Molecular Weight: 142.24166000
Formula: C9 H18 O
BioActivity Summary: listing
NMR Predictor: Predict (works with chrome or firefox)
EFSA/JECFA Comments: JECFA name: 3,3,5-Trimethyl cyclohexanol. Racemate (EFFA, 2010a).
Category: flavor and fragrance agents
 
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Google Scholar: Search
Google Books: Search
Google Scholar: with word "volatile"Search
Google Scholar: with word "flavor"Search
Google Scholar: with word "odor"Search
Perfumer and Flavorist: Search
Google Patents: Search
US Patents: Search
EU Patents: Search
Pubchem Patents: Search
PubMed: Search
NCBI: Search
JECFA Food Flavoring: 1099  3,3,5-trimethyl cyclohexanol
FLAVIS Number: 02.209 (Old)
DG SANTE Food Flavourings: 02.209  3,3,5-trimethylcyclohexan-1-ol
FEMA Number: 3962  3,3,5-trimethylcyclohexanol
FDA:No longer provide for the use of these seven synthetic flavoring substances
FDA Mainterm (SATF):116-02-9 ; 3,3,5-TRIMETHYLCYCLOHEXANOL
Synonyms   Articles   Notes   Search   Top
Physical Properties:
Appearance: white crystals (est)
Assay: 98.00 to 100.00 % sum of isomers
Food Chemicals Codex Listed: No
Melting Point: 30.00 to  34.00 °C. @ 760.00 mm Hg
Boiling Point: 80.00 °C. @ 20.00 mm Hg
Boiling Point: 193.00 to  196.00 °C. @ 760.00 mm Hg
Acid Value: 1.00 max. KOH/g
Vapor Pressure: 0.173000 mmHg @ 25.00 °C. (est)
Flash Point: 180.00 °F. TCC ( 82.22 °C. )
logP (o/w): 2.734 (est)
Soluble in:
 water, 840.8 mg/L @ 25 °C (est)
Synonyms   Articles   Notes   Search   Top
Organoleptic Properties:
 
Odor Type: minty
 
Odor Strength: medium
 
Substantivity: 20 hour(s) at 100.00 %
 
 minty  cooling  mentholic  musty  spicy  
Odor Description:
at 100.00 %. 
mint cool mentholic musty spicy
Luebke, William tgsc, (1986)
 
 
Flavor Type: minty
 
 mentholic  cooling  minty  spicy  
Taste Description:
mentholic cooling minty spicy
 
Odor and/or flavor descriptions from others (if found).
 
 
Synonyms   Articles   Notes   Search   Top
Cosmetic Information:
CosIng: cosmetic data
Cosmetic Uses: perfuming agents
Synonyms   Articles   Notes   Search   Top
Suppliers:
EMD Millipore
For experimental / research use only.
3,3,5-Trimethylcyclohexanol
Inoue Perfumery
3,3,5-TRIMETHYLCYCLOHEXANOL
Lluch Essence
TRIMETHYLCYCLOHEXANOL MIX
Moellhausen
3,3,5-TRIMETHYLCYCLOHEXANOL
Penta International
3,3,5-TRIMETHYLCYCLOHEXANOL
Santa Cruz Biotechnology
For experimental / research use only.
3,3,5-Trimethylcyclohexanol
Sigma-Aldrich: Aldrich
For experimental / research use only.
3,3,5-Trimethylcyclohexanol
TCI AMERICA
For experimental / research use only.
3,3,5-Trimethylcyclohexanol (cis- and trans- mixture) >90.0%(GC)
Vigon International
Trimethyl-3,3,5 Cyclohexanol (Homomenthol)
Odor: Mint cool mentholic musty spicy
Synonyms   Articles   Notes   Search   Top
Safety Information:
Preferred SDS: View
European information :
Most important hazard(s):
Xi - Irritant
R 37/38 - Irritating to respiratory system and skin.
R 41 - Risk of serious damage to eyes.
S 02 - Keep out of the reach of children.
S 24/25 - Avoid contact with skin and eyes.
S 26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S 37/39 - Wear suitable gloves and eye/face protection.
 
Hazards identification
 
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
None found.
GHS Label elements, including precautionary statements
 
Pictogram
 
Hazard statement(s)
None found.
Precautionary statement(s)
None found.
Oral/Parenteral Toxicity:
oral-rat LD50  [sex: M,F] 3250 mg/kg
(Smyth & Carpenter, 1948)

oral-rat LD50  3250 mg/kg
Journal of Industrial Hygiene and Toxicology. Vol. 31, Pg. 60, 1949.

Dermal Toxicity:
skin-rabbit LD50 2800 mg/kg
Journal of Industrial Hygiene and Toxicology. Vol. 31, Pg. 60, 1949.

Inhalation Toxicity:
Not determined
Synonyms   Articles   Notes   Search   Top
Safety in Use Information:
Category: flavor and fragrance agents
IFRA Code of Practice Notification of the 49th Amendment to the IFRA Code of Practice
Recommendation for homomenthol usage levels up to:
  4.0000 % in the fragrance concentrate.
 
Maximised Survey-derived Daily Intakes (MSDI-EU): 0.12 (μg/capita/day)
Maximised Survey-derived Daily Intakes (MSDI-USA): 0.10 (μg/capita/day)
Structure Class: I
Use levels for FEMA GRAS flavoring substances on which the FEMA Expert Panel based its judgments that the substances are generally recognized as safe (GRAS).
The Expert Panel also publishes separate extensive reviews of scientific information on all FEMA GRAS flavoring substances and can be found at FEMA Flavor Ingredient Library
publication number: 19
Click here to view publication 19
 average usual ppmaverage maximum ppm
baked goods: 0.100000.20000
beverages(nonalcoholic): 0.400001.00000
beverages(alcoholic): --
breakfast cereal: --
cheese: --
chewing gum: --
condiments / relishes: --
confectionery froastings: 0.500001.00000
egg products: --
fats / oils: --
fish products: --
frozen dairy: 1.000002.00000
fruit ices: --
gelatins / puddings: 0.500001.00000
granulated sugar: --
gravies: --
hard candy: --
imitation dairy: --
instant coffee / tea: --
jams / jellies: --
meat products: --
milk products: --
nut products: --
other grains: --
poultry: --
processed fruits: --
processed vegetables: --
reconstituted vegetables: --
seasonings / flavors: --
snack foods: --
soft candy: 2.000005.00000
soups: --
sugar substitutes: --
sweet sauces: --
Synonyms   Articles   Notes   Search   Top
Safety References:
European Food Safety Athority(efsa): Flavor usage levels; Subacute, Subchronic, Chronic and Carcinogenicity Studies; Developmental / Reproductive Toxicity Studies; Genotoxicity Studies...
European Food Safety Authority (EFSA) reference(s):
Flavouring Group Evaluation 51, (FGE.51)[1] - Consideration of alicyclic ketones and secondary alcohols and related esters evaluated by JECFA (59th meeting) and structurally related to alicyclic ketones, secondary alcohols and related esters evaluated by EFSA in FGE.09 (2004) - Opinion of the Scientific Panel on Food Additives, Flavourings, Processing Aids and Materials in Contact with Food
View page or View pdf
Flavouring Group Evaluation 9, Revision 1: (FGE.09 Rev1)[1] - Secondary alicyclic saturated and unsaturated alcohols, ketones and esters containing secondary alicyclic alcohols from chemical groups 8 and 30, and an ester of a phenol carboxylic acid from chemical group 25 - Scientific Opinion of the Panel on Food Additives, Flavourings, Processing Aids and Materials in Contact with Food
View page or View pdf
Flavouring Group Evaluation 9, Revision 2 (FGE.09Rev2): Secondary alicyclic saturated and unsaturated alcohols, ketones and esters containing secondary alicyclic alcohols from chemical group 8 and 30, and an ester of a phenol derivative from chemical group 25
View page or View pdf
Scientific Opinion on Flavouring Group Evaluation 51, Revision 1 (FGE.51Rev1): Consideration of alicyclic ketones and secondary alcohols and related esters evaluated by the JECFA (59th meeting) structurally related to alicyclic ketones secondary alcohols and related esters in FGE.09Rev3 (2011)
View page or View pdf
Flavouring Group Evaluation 51, Revision 2 (FGE.51Rev2): Consideration of alicyclic ketones and secondary alcohols and related esters evaluated by JECFA (59th meeting) structurally related to alicyclic ketones secondary alcohols and related esters in FGE.09Rev6 (2015)
View page or View pdf
EPI System: View
NLM Hazardous Substances Data Bank: Search
EPA Substance Registry Services (TSCA): 116-02-9
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 8298
National Institute of Allergy and Infectious Diseases: Data
WGK Germany: 1
 3,3,5-trimethylcyclohexan-1-ol
Chemidplus: 0000116029
RTECS: GW0875000 for cas# 116-02-9
Synonyms   Articles   Notes   Search   Top
References:
 3,3,5-trimethylcyclohexan-1-ol
NIST Chemistry WebBook: Search Inchi
Canada Domestic Sub. List: 116-02-9
Pubchem (cid): 8298
Pubchem (sid): 134975364
Synonyms   Articles   Notes   Search   Top
Other Information:
(IUPAC): Atomic Weights of the Elements 2009
(IUPAC): Atomic Weights of the Elements 2009 (pdf)
Videos: The Periodic Table of Videos
tgsc: Atomic Weights use for this web site
(IUPAC): Periodic Table of the Elements
FDA Substances Added to Food (formerly EAFUS): View
CHEBI: View
CHEMBL: View
HMDB (The Human Metabolome Database): HMDB29557
FooDB: FDB000708
Export Tariff Code: 2906.12.0000
Haz-Map: View
ChemSpider: View
Wikipedia: View
RSC Learn Chemistry: View
Synonyms   Articles   Notes   Search   Top
Potential Blenders and core components note
 
For Odor
No odor group found for these
 fenchoneFL/FR
 laurel leaf concreteFR
 yarrow oil greeceFL/FR
 yarrow oil hungaryFL/FR
 camphenilone 
 feverfew leaf oil belgium 
 laurel leaf absoluteFL/FR
laevo-monomenthyl glutarateFL/FR
2-methyl-3-butanoneFL/FR
 xanthoxylin 
 yarrow oilFL/FR
anisic
bitter fennel seed oil spainFR
balsamic
dextro,laevo-borneolFL/FR
dextro,laevo-isoborneolFL/FR
dextro-borneolFL/FR
laevo-borneolFL/FR
isobornyl acetateFL/FR
isobornyl formateFL/FR
isobornyl methyl etherFL/FR
isobornyl propionateFL/FR
dextro-fenchoneFL/FR
camphoreous
3-benzylidene-2-butanoneFL/FR
 bornyl isobutyrateFL/FR
 butyrophenoneFL/FR
alpha-campholenic alcoholFL/FR
dextro-camphorFL/FR
(±)-camphorFL/FR
 camphor tree bark oilFL/FR
beta-homocyclocitralFL/FR
 fencholFL/FR
laevo-fenchoneFL/FR
 herbal ethanoneFR
 hinoki leaf oilFR
 thujyl alcoholFL/FR
 verbenoneFL/FR
citrus
 ocimene quintoxideFL/FR
earthy
2-ethyl fencholFL/FR
ethereal
 methyl ethyl ketoneFL/FR
floral
 dihydrocarvyl acetateFL/FR
 dihydrolinaloolFL/FR
 linalool oxide (furanoid)FL/FR
fruity
 cherry propanolFL/FR
herbal
1-allyl-2,2,7,7-tetramethyl cycloheptanolFR
 barosma betulina leaf oilFL/FR
(-)-bornyl isovalerateFL/FR
 chamomile oil moroccoFR
1,8-cineoleFL/FR
1,4-cineoleFL/FR
 dehydroxylinalool oxideFL/FR
 dimethyl cyclormol (IFF)FR
2,10-epoxypinaneFR
 eucalyptus globulus oilFL/FR
 geranic oxideFL/FR
 herbal dioxaneFR
 herbal undecanolFR
6-hydroxydihydrotheaspirane (mixture of isomers)FL/FR
 hyssop oilFL/FR
 laurel bark oil 
 laurel stem oil 
 lavandin concreteFL/FR
abrialis lavandin oilFL/FR
spike lavender absoluteFL/FR
spike lavender oilFL/FR
spike lavender oil spainFL/FR
 melaleuca leucadendron var. cajuputi leaf oilFL/FR
 methyl cyclogeranate (Firmenich)FR
 myrtenolFL/FR
 myrtle oilFL/FR
 niaouli oilFR
 origanum oilFL/FR
 origanum oil greeceFL/FR
 pine hexanolFR
alpha-pineneFL/FR
 pinocarveolFL/FR
 piperitoneFL/FR
 rosemary absoluteFL/FR
 rosemary oil egyptFL/FR
 rosemary oil moroccoFL/FR
 rosemary oil spainFL/FR
 sabinene hydrateFL/FR
 sage absolute spainFL/FR
 theaspiraneFL/FR
white thyme oilFL/FR
 thyme oil (thymus zygis gracillis) spainFL/FR
 thymolFL/FR
mentholic
 cornmint oil chinaFL/FR
 cornmint oil terpenelessFL/FR
dextro,laevo-mentholFL/FR
dextro-neomentholFL/FR
(±)-mentholFL/FR
(±)-isomenthoneFL/FR
laevo-menthyl acetateFL/FR
 menthyl acetate racemicFL/FR
 peppermint cyclohexanoneFL/FR
dextro-piperitoneFL/FR
minty
 camphene hydrate 
dextro-carvoneFL/FR
cis-carvone-5,6-oxideFL/FR
 cornmint oil japanFL/FR
dextro-dihydrocarvoneFL/FR
(-)-menthoneFL/FR
(±)-menthoneFL/FR
laevo-menthyl lactateFL/FR
 pennyroyal oil fractionsFL/FR
 peppermint absoluteFL/FR
 peppermint oil americaFL/FR
 peppermint oil idahoFL/FR
isopropyl tiglateFL/FR
(-)-isopulegolFL/FR
isopulegolFL/FR
(R)-(+)-pulegoneFR
naphthyl
ortho-methyl anisoleFL/FR
1-methyl naphthaleneFL/FR
 carvacrolFL/FR
 elettaria cardamomum seed oilFL/FR
 galangal root oilFL/FR
 laurel berry absoluteFL/FR
 laurus nobilis fruit oilFL/FR
 laurus nobilis leaf oilFL/FR
 laurus nobilis leaf oil turkeyFL/FR
 marjoram absolute spain 
 marjoram oil (thymus mastichina) spainFL/FR
 myrtenalFL/FR
 origanum majorana oilFL/FR
 origanum majorana oil cubaFL/FR
white sassafras oilFL/FR
 sugandha kokila berry oilFR
 tea tree oilFR
laevo-verbenoneFL/FR
 zvoulimba leaf oilFR
thujonic
 armoise oilFR
 cedarleaf oil terpenelessFR
 sage oil (salvia lavandulifolia vahl.) spainFL/FR
woody
isobornyl isovalerateFL/FR
 bornyl valerateFL/FR
2-tert-butyl cyclohexanoneFR
 campheneFL/FR
(+)-campheneFL/FR
 hinoki root oilFR
 orris hexanoneFR
 patchouli ethanolFR
 patchouli hexanolFR
 sandal glycol acetalFR
 zedoary bark oilFL/FR
 
For Flavor
 
No flavor group found for these
3-benzylidene-2-butanoneFL/FR
dextro-borneolFL/FR
dextro,laevo-borneolFL/FR
 bornyl isobutyrateFL/FR
(-)-bornyl isovalerateFL/FR
isobornyl methyl etherFL/FR
 butyrophenoneFL/FR
(+)-campheneFL/FR
 camphene hydrate 
 camphenilone 
alpha-campholenic alcoholFL/FR
 capsicum oleoresin CO2 extractFL
 epoxyoxophoroneFL
 fenchoneFL/FR
 feverfew leaf oil belgium 
 laurel bark oil 
 laurel berry absoluteFL/FR
 laurel stem oil 
 laurus nobilis fruit oilFL/FR
 laurus nobilis leaf oilFL/FR
 laurus nobilis leaf oil turkeyFL/FR
 linalool oxide (furanoid)FL/FR
 marjoram absolute spain 
 melaleuca leucadendron var. cajuputi leaf oilFL/FR
 menthyl acetate racemicFL/FR
laevo-monomenthyl glutarateFL/FR
 menthyl propylene glycol carbonateFL
3-methyl cyclohexanoneFL
2-methyl-3-butanoneFL/FR
(Z,Z)-photocitral AFL
white sassafras oilFL/FR
laevo-verbenoneFL/FR
 verbenoneFL/FR
 xanthoxylin 
 yarrow oilFL/FR
 yarrow oil greeceFL/FR
 yarrow oil hungaryFL/FR
 laurel leaf absoluteFL/FR
 thujyl alcoholFL/FR
balsamic
isobornyl propionateFL/FR
camphoreous
dextro,laevo-isoborneolFL/FR
laevo-borneolFL/FR
 campheneFL/FR
(±)-camphorFL/FR
 camphor tree bark oilFL/FR
 fencholFL/FR
laevo-fenchoneFL/FR
 geranic oxideFL/FR
6-hydroxydihydrotheaspirane (mixture of isomers)FL/FR
ortho-methyl anisoleFL/FR
 pinocarveolFL/FR
chemical
 methyl ethyl ketoneFL/FR
cooling
1,4-cineoleFL/FR
beta-homocyclocitralFL/FR
dextro-fenchoneFL/FR
spike lavender oilFL/FR
dextro,laevo-mentholFL/FR
isomentholFL
laevo-menthyl lactateFL/FR
 peppermint oil americaFL/FR
 sabinene hydrateFL/FR
 theaspiraneFL/FR
 WS-3FL
 WS-5FL
earthy
2-ethyl fencholFL/FR
floral
 dihydrocarvyl acetateFL/FR
 dihydrolinaloolFL/FR
fruity
 cherry propanolFL/FR
green
dextro-dihydrocarvoneFL/FR
 ocimene quintoxideFL/FR
isopropyl tiglateFL/FR
herbal
 barosma betulina leaf oilFL/FR
 eucalyptus globulus oilFL/FR
 hyssop oilFL/FR
 lavandin concreteFL/FR
abrialis lavandin oilFL/FR
spike lavender absoluteFL/FR
spike lavender oil spainFL/FR
 origanum majorana oilFL/FR
 origanum oilFL/FR
 origanum oil greeceFL/FR
 rosemary absoluteFL/FR
 rosemary oil egyptFL/FR
 rosemary oil moroccoFL/FR
 rosemary oil spainFL/FR
 sage absolute spainFL/FR
 sage oil (salvia lavandulifolia vahl.) spainFL/FR
white thyme oilFL/FR
 thyme oil (thymus zygis gracillis) spainFL/FR
medicinal
dextro-camphorFL/FR
mentholic
 cornmint oil terpenelessFL/FR
dextro-neomentholFL/FR
(±)-mentholFL/FR
 peppermint cyclohexanoneFL/FR
minty
dextro-carvoneFL/FR
cis-carvone-5,6-oxideFL/FR
1,8-cineoleFL/FR
 cornmint oil chinaFL/FR
 cornmint oil japanFL/FR
(-)-menthoneFL/FR
(±)-isomenthoneFL/FR
(±)-menthoneFL/FR
laevo-menthyl acetateFL/FR
 myrtenalFL/FR
 myrtenolFL/FR
 pennyroyal oil fractionsFL/FR
 peppermint absoluteFL/FR
 peppermint oil idahoFL/FR
 piperitoneFL/FR
dextro-piperitoneFL/FR
(-)-isopulegolFL/FR
isopulegolFL/FR
naphthyl
1-methyl naphthaleneFL/FR
phenolic
 thymolFL/FR
spicy
 carvacrolFL/FR
 cubeb oleoresinFL
 elettaria cardamomum seed oilFL/FR
 galangal root oilFL/FR
 marjoram oil (thymus mastichina) spainFL/FR
 myrtle oilFL/FR
 origanum majorana oil cubaFL/FR
woody
isobornyl acetateFL/FR
isobornyl formateFL/FR
isobornyl isovalerateFL/FR
 bornyl valerateFL/FR
 dehydroxylinalool oxideFL/FR
alpha-pineneFL/FR
 zedoary bark oilFL/FR
 
Synonyms   Articles   Notes   Search   Top
Potential Uses:
 camphor tree barkFL/FR
 cistusFL/FR
 coolingFL
 eucalyptus oil replacerFR
 hay new mown hayFR
 herbalFR
 mintFR
 pennyroyalFL/FR
 peppermintFR
Synonyms   Articles   Notes   Search   Top
Occurrence (nature, food, other): note
 not found in nature
Synonyms   Articles   Notes   Search   Top
Synonyms:
 cyclohexanol, 3,3,5-trimethyl-
 cyclonol
 dihydroisophorol
homomenthol
1-methyl-3-dimethyl cyclohexanol-5
 TMCH
3,3,5-trimethyl cyclohexan-1-ol
3,3,5-trimethyl cyclohexanol
3,3,5-trimethyl-1-cyclohexanol
 trimethyl-3 3 5 cyclohexanol
3,3,5-trimethyl-cyclohexanol
3,3,5-trimethylcyclohexan-1-ol
3,3,5-trimethylcyclohexanol
3,5,5-trimethylcyclohexanol
Synonyms   Articles   Notes   Search   Top
Synonyms   Articles   Notes   Search   Top
Please share your Comments.
Email Address:
 
 
 
 
Top of Page Home
Copyright © 1980-2020 Perflavory ™ Disclaimer Privacy Policy