trans-para-menthane-3,8-diol
cyclohexanemethanol, 2-hydroxy-a,a,4-trimethyl-,(1R,2R)-rel-
 
Notes:
None found
  • BOC Sciences
    • BOC Sciences
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      Product(s):
      3564-98-5 Trans-p-Menthane-3,8-diol 95+%
       
  • Glentham Life Sciences
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CAS Number: 3564-98-5Picture of molecule3D/inchi
Other(deleted CASRN): 81176-88-7
FDA UNII: EB999AF32A
Beilstein Number: 5240317
MDL: MFCD00191552
XlogP3-AA: 2.20 (est)
Molecular Weight: 172.26780000
Formula: C10 H20 O2
NMR Predictor: Predict (works with chrome, Edge or firefox)
Category: natural substances and extractives
 
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
Google Patents: Search
US Patents: Search
EU Patents: Search
Pubchem Patents: Search
PubMed: Search
NCBI: Search
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Physical Properties:
Appearance: white crystals (est)
Assay: 98.00 to 100.00 % 
Food Chemicals Codex Listed: No
Melting Point: 34.00 to  35.00 °C. @ 760.00 mm Hg
Boiling Point: 267.00 to  268.00 °C. @ 760.00 mm Hg
Vapor Pressure: 0.001000 mmHg @ 25.00 °C. (est)
Flash Point: 249.00 °F. TCC ( 120.56 °C. )
logP (o/w): 1.607 (est)
Soluble in:
 alcohol
 water, 670.7 mg/L @ 25 °C (est)
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Organoleptic Properties:
 
Odor Type: herbal
 
 herbal  eucalyptus  minty  
Odor Description:
at 100.00 %. 
herbal eucalyptus minty
 
Odor and/or flavor descriptions from others (if found).
 
 
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Cosmetic Information:
None found
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Suppliers:
BOC Sciences
For experimental / research use only.
Trans-p-Menthane-3,8-diol 95+%
Glentham Life Sciences
trans-p-Menthane-3,8-diol
Santa Cruz Biotechnology
For experimental / research use only.
trans-p-Menthane-3,8-diol 95%
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Safety Information:
Preferred SDS: View
 
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:
Not determined
Dermal Toxicity:
subcutaneous-mouse LD50 1240 mg/kg
BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD
Sapporo Igaku Zasshi. Sapporo Medical Journal. Vol. 3, Pg. 73, 1952.

Inhalation Toxicity:
Not determined
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Safety in Use Information:
Category: natural substances and extractives
Recommendation for trans-para-menthane-3,8-diol usage levels up to:
 not for fragrance use.
 
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
 average usual ppmaverage maximum ppm
baked goods: --
beverages(nonalcoholic): 5.0000025.00000
beverages(alcoholic): 5.0000025.00000
breakfast cereal: 5.0000020.00000
cheese: 5.0000025.00000
chewing gum: 75.00000150.00000
condiments / relishes: 5.0000025.00000
confectionery froastings: 5.0000025.00000
egg products: --
fats / oils: 5.0000025.00000
fish products: --
frozen dairy: 5.0000025.00000
fruit ices: 5.0000025.00000
gelatins / puddings: 10.0000050.00000
granulated sugar: --
gravies: 5.0000035.00000
hard candy: 30.00000100.00000
imitation dairy: 5.0000035.00000
instant coffee / tea: --
jams / jellies: 10.0000050.00000
meat products: --
milk products: --
nut products: 10.0000050.00000
other grains: --
poultry: --
processed fruits: 5.0000025.00000
processed vegetables: 5.0000025.00000
reconstituted vegetables: 5.0000025.00000
seasonings / flavors: --
snack foods: 5.0000025.00000
soft candy: 10.0000050.00000
soups: 7.0000035.00000
sugar substitutes: --
sweet sauces: 5.0000050.00000
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Safety References:
EPI System: View
AIDS Citations: Search
Cancer Citations: Search
Toxicology Citations: Search
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 21310069
National Institute of Allergy and Infectious Diseases: Data
 (1R,2R)-2-(2-hydroxypropan-2-yl)-5-methylcyclohexan-1-ol
Chemidplus: 0003564985
RTECS: OS9110000 for cas# 3564-98-5
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References:
 (1R,2R)-2-(2-hydroxypropan-2-yl)-5-methylcyclohexan-1-ol
NIST Chemistry WebBook: Search Inchi
Pubchem (cid): 21310069
Pubchem (sid): 134984565
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Other Information:
(IUPAC): Atomic Weights of the Elements 2011 (pdf)
Videos: The Periodic Table of Videos
tgsc: Atomic Weights use for this web site
(IUPAC): Periodic Table of the Elements
CHEBI: View
KEGG (GenomeNet): C02904
HMDB (The Human Metabolome Database): Search
VCF-Online: VCF Volatile Compounds in Food
ChemSpider: View
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Potential Blenders and core components note
 
For Odor
anisic
 estragoleFL/FR
camphoreous
 herbal ethanoneFR
citrus
 petitgrain combava oilFR
floral
 menthadienyl formateFR
1,8-cineoleFL/FR
ortho-cresyl salicylateFL/FR
isodihydrolavandulolFR
(Z)-isodihydrolavandulyl acetateFR
 herbal undecaneFR
 herbal undecanolFR
 hyssop oilFL/FR
spike lavender oilFL/FR
spike lavender oil spainFL/FR
 melaleuca leucadendron cajaputi oilFL/FR
 niaouli oilFR
 piperitoneFL/FR
 rosemary absoluteFL/FR
 sabinene hydrateFL/FR
mentholic
 cornmint oilFL/FR
laevo-menthyl acetateFL/FR
minty
homomenthyl acetateFL/FR
spicy
 elettaria cardamomum seed oilFL/FR
 marjoram oil (thymus mastichina) spainFL/FR
thujonic
 sage oil dalmatianFL/FR
 
For Flavor
 
No flavor group found for these
ortho-cresyl salicylateFL/FR
 piperitenone oxideFL
cooling
spike lavender oilFL/FR
homomenthyl acetateFL/FR
 sabinene hydrateFL/FR
herbal
2-acetoxy-1,8-cineoleFL
 hyssop oilFL/FR
spike lavender oil spainFL/FR
 melaleuca leucadendron cajaputi oilFL/FR
 rosemary absoluteFL/FR
licorice
 estragoleFL/FR
mentholic
 cornmint oilFL/FR
minty
1,8-cineoleFL/FR
laevo-menthyl acetateFL/FR
 piperitoneFL/FR
spicy
 elettaria cardamomum seed oilFL/FR
 marjoram oil (thymus mastichina) spainFL/FR
thujonic
 sage oil dalmatianFL/FR
 
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Potential Uses:
 eucalyptus oil replacerFR
 herbalFR
 papayaFR
 rosemaryFR
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Occurrence (nature, food, other): note
 found in nature
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Synonyms:
 cyclohexanemethanol, 2-hydroxy-a,a,4-trimethyl-,(1R,2R)-rel-
 cyclohexanemethanol, 2-hydroxy-a,a,4-trimethyl-, (1R,2R)-
(1R,2R)-2-(1-hydroxy-1-methylethyl)-5-methylcyclohexanol
(1R,2R)-2-hydroxy-a,a,4-trimethylcyclohexanemethanol
(1-alpha,2-beta,4-beta)-2-hydroxy-alpha,alpha,4-trimethyl cyclohexane methanol
(1R,2R)-2-hydroxy-alpha,alpha,4-trimethyl cyclohexane methanol
(1-alpha,2-beta,4-beta)-2-hydroxy-alpha,alpha,4-trimethylcyclohexanemethanol
(1R,2R)-2-hydroxy-alpha,alpha,4-trimethylcyclohexanemethanol
(1R,2R)-2-(2-hydroxypropan-2-yl)-5-methylcyclohexan-1-ol
(1R,2R)-2-(2-hydroxypropan-2-yl)-5-methylcyclohexanol
(1R,3R)-p-menthan-3,8-diol
cis-1,3,trans-1,4-p-menthan-3,8-diol
cis-1,3,trans-1,4-para-menthan-3,8-diol
trans-p-menthan-3,8-diol
trans-para-menthan-3,8-diol
p-menthan-3,8-diol, cis-1,3,trans-1,4-
(1R,3R)-p-menthane-3,8-diol
cis-1,3,trans-1,4-p-menthane-3,8-diol
cis-1,3,trans-1,4-para-menthane-3,8-diol
trans-p-menthane-3,8-diol
p-menthane-3,8-diol, cis-1,3,trans-1,4-
 menthoglycol
(-)-isopulegol hydrate
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