EU/US Properties Organoleptics Cosmetics Suppliers Safety Safety in use Safety references References Other Blenders Uses Occurrence Synonyms Articles Notes
 

tetrahydroionol
cyclohexanepropanol, a,2,2,6-tetramethyl-

Supplier Sponsors

Name:4-(2,2,6-trimethylcyclohexyl)butan-2-ol
CAS Number: 4361-23-3Picture of molecule3D/inchi
ECHA EINECS - REACH Pre-Reg:224-445-7
Nikkaji Web:J191.440E
XlogP3-AA:4.30 (est)
Molecular Weight:198.34942000
Formula:C13 H26 O
NMR Predictor:Predict (works with chrome or firefox)
Category: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
 
Physical Properties:
Appearance:colorless clear liquid (est)
Assay: 98.00 to 100.00 sum of isomers
Food Chemicals Codex Listed: No
Specific Gravity:0.90000 to 0.81500 @ 25.00 °C.
Pounds per Gallon - (est).: 7.489 to 6.782
Boiling Point: 80.00 °C. @ 2.00 mm Hg
Boiling Point: 250.00 to 251.00 °C. @ 760.00 mm Hg
Vapor Pressure:0.004000 mmHg @ 25.00 °C. (est)
Flash Point: 220.00 °F. TCC ( 104.44 °C. )
logP (o/w): 4.616 (est)
Soluble in:
 alcohol
 water, 11.11 mg/L @ 25 °C (est)
Insoluble in:
 water
 
Organoleptic Properties:
Odor Type: floral
Odor Strength:medium
Substantivity: > 8 hour(s) at 100.00 %
floral violet woody leathery
Odor Description:at 100.00 %. mild floral violet woody leathery
Odor and/or flavor descriptions from others (if found).
Bedoukian Research
TETRAHYDROIONOL ≥97.0%, Kosher, Special Order
Odor Description:A mild floral, violet odor
Used mostly in woody and violet applications.
Nactis Flavours
TETRAHYDROIONOL
Odor Description:rich violet, woody and leathery note
 
Cosmetic Information:
CosIng:cosmetic data
Cosmetic Uses: perfuming agents
 
Suppliers:
Associate Allied Chemicals
Tetrahydro Ionol
About
Bedoukian Research
TETRAHYDROIONOL
≥97.0%, Kosher, Special Order
Odor: A mild floral, violet odor
Use: Used mostly in woody and violet applications.
BOC Sciences
For experimental / research use only.
TETRAHYDROIONOL 97.0%
Nactis Flavours
TETRAHYDROIONOL
Odor: rich violet, woody and leathery note
Penta International
TETRAHYDROIONOL
 
Safety Information:
European information :
Most important hazard(s):
Xi - Irritant
R 36/38 - Irritating to skin and 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 36 - Wear suitable protective clothing.
 
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:
Not determined
Inhalation Toxicity:
Not determined
 
Safety in Use Information:
Category: fragrance agents
Recommendation for tetrahydroionol usage levels up to:
  5.0000 % in the fragrance concentrate.
 
Recommendation for tetrahydroionol flavor usage levels up to:
 not for flavor use.
 
Safety References:
EPI System: View
EPA Substance Registry Services (TSCA):4361-23-3
EPA ACToR:Toxicology Data
EPA Substance Registry Services (SRS):Registry
Laboratory Chemical Safety Summary :107272
National Institute of Allergy and Infectious Diseases:Data
WGK Germany:1
4-(2,2,6-trimethylcyclohexyl)butan-2-ol
Chemidplus:0004361233
 
References:
Leffingwell:Chirality or Article
 4-(2,2,6-trimethylcyclohexyl)butan-2-ol
NIST Chemistry WebBook:Search Inchi
Canada Domestic Sub. List:4361-23-3
Pubchem (cid):107272
Pubchem (sid):135063055
 
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
HMDB (The Human Metabolome Database):Search
Export Tariff Code:2906.19.5000
ChemSpider:View
 
Potential Blenders and core components note
For Odor
No odor group found for these
(E+Z)-4,8-
dimethyl-3,7-nonadien-2-one
FL/FR
(E)-beta-
methyl ionone
FL/FR
alliaceous
alliaceous
dibutyl sulfide
FL/FR
animal
2-iso
butyl quinoline
FR
methyl (E)-2-octenoate
FL/FR
balsamic
benzyl cinnamate
FL/FR
citrus
citronellone
FR
2-
heptanol
FL/FR
fatty
butyl undecylenate
FL/FR
floral
acetal 318
FR
iso
amyl angelate
FL/FR
alpha-
amyl cinnamaldehyde
FL/FR
benzyl acetate
FL/FR
benzyl acetoacetate
FL/FR
benzyl formate
FL/FR
boronia absolute
FL/FR
boronia absolute replacer
FL/FR
boronia butenal
FR
boronia fragrance
FR
cassie absolute
FL/FR
cassie concrete
FR
dihydro-alpha-ionone
FL/FR
dimethyl alpha-ionone
FR
dimethyl benzyl carbinyl acetate
FL/FR
4-
dimethyl ionone
FR
floral methanol
FR
geraniol
FL/FR
hugonia specialty
FR
beta-
ionol
FL/FR
alpha-
ionol
FL/FR
alpha-
ionone
FL/FR
alpha-
ionyl acetate
FR
beta-
ionyl acetate
FL/FR
iris specialty
FR
alpha-
irone
FL/FR
menthadienyl formate
FR
ortho-
methoxybenzyl ethyl ether
FR
methoxymelonal
FL/FR
methyl benzyl acetate (mixed ortho-,meta-,para-)
FL/FR
beta-iso
methyl ionone
FL/FR
N-
methyl ionone
FR
alpha-iso
methyl ionone (50% min.)
FL/FR
alpha-iso
methyl ionone (60% min.)
FL/FR
alpha-iso
methyl ionone (70% min.)
FL/FR
alpha-iso
methyl ionone (80% min.)
FL/FR
alpha-iso
methyl ionone (90% min.)
FL/FR
methyl ionyl acetate
FL/FR
muguet carbinol
FL/FR
orris butenone
FR
orris pyridine 25% IPM
FR
orris rhizome absolute (iris germanica)
FL/FR
orris rhizome absolute (iris pallida)
FL/FR
orris rhizome concrete butter (iris pallida)
FL/FR
orris rhizome oil (iris germanica)
FL/FR
orris rhizome resinoid (iris pallida)
FL/FR
orris rhizome resinoid replacer
FR
petitgrain lemon oil
FL/FR
phenethyl isobutyrate
FL/FR
phenethyl isovalerate
FL/FR
star fruit oil cuba
FL/FR
tobacco flower absolute
FR
violet flower absolute
FL/FR
violet methyl carbonate
FR
fruity
beta-
ionone epoxide
FL/FR
3-
mercaptohexyl acetate
FL/FR
rhubarb pyran
FR
green
iso
amyl 3-(2-furan) propionate
FL/FR
1-
heptanol
FL/FR
(Z)-3-
hexen-1-yl (Z)-3-hexenoate
FL/FR
(Z)-3-
hexen-1-yl methyl carbonate
FL/FR
hexen-1-yl oxypropane nitrile
FR
hexoxyacetaldehyde dimethyl acetal
FR
(Z)-
leaf acetal
FL/FR
melon nonenoate
FL/FR
methyl heptine carbonate
FL/FR
methyl octine carbonate
FL/FR
3,6-
nonadien-1-ol
FL/FR
(E,Z)-2,6-
nonadien-1-ol
FL/FR
2,6-
nonadienal
FL/FR
(E,Z)-2,6-
nonadienal
FL/FR
(E)-2-
nonen-1-ol
FL/FR
2-
nonyn-1-al dimethyl acetal
FR
octanal dimethyl acetal
FL/FR
violet decenol
FR
violet dienyne
FR
violet leaf absolute
FL/FR
violet leaf concrete
FR
violet nitrile
FR
herbal
cananga fruit oil
FR
chamomile valerate
FR
clary propyl acetate
FR
methyl cyclogeranate (Firmenich)
FR
orris
beta-
methyl ionone
FL/FR
2(1)-
orris butanal
FL/FR
phenolic
meta-
cresol
FR
powdery
dimethyl ionone
FR
alpha-
methyl ionone
FL/FR
(E)-alpha-
methyl ionone (44-50%)
FL/FR
(E)-alpha-
methyl ionone (50-60%)
FL/FR
(E)-alpha-
methyl ionone (74-80%)
FL/FR
resinous
amber oil CO2 extract
FR
smoky
birch tar oil
FL/FR
tobacco
veltonal (Bedoukian)
FR
tonka
saffron resinoid
FL/FR
waxy
ethyl myristate
FL/FR
orris rhizome oil CO2 extract
FL/FR
woody
diethyl dimethyl-2-cyclohexenone
FR
1-(5',5',6'-
trimethyl bicyclo(2.2.1)hept-2'-yl) propan-2-one
FR
violet propanol
FR
(Z)-
woody amylene
FR
For Flavor
No flavor group found for these
iso
amyl angelate
FL/FR
birch tar oil
FL/FR
boronia absolute replacer
FL/FR
(E+Z)-4,8-
dimethyl-3,7-nonadien-2-one
FL/FR
beta-
ionone epoxide
FL/FR
methyl benzyl acetate (mixed ortho-,meta-,para-)
FL/FR
beta-iso
methyl ionone
FL/FR
(E)-beta-
methyl ionone
FL/FR
(E)-alpha-
methyl ionone (44-50%)
FL/FR
(E)-alpha-
methyl ionone (50-60%)
FL/FR
alpha-iso
methyl ionone (60% min.)
FL/FR
2,6-
nonadienal
FL/FR
2(1)-
orris butanal
FL/FR
iso
amyl 3-(2-furan) propionate
FL/FR
benzyl acetoacetate
FL/FR
apple
apple
(E,Z)-2,6-
nonadien-1-ol
FL/FR
berry
dihydro-alpha-ionone
FL/FR
citrus
petitgrain lemon oil
FL/FR
floral
dimethyl benzyl carbinyl acetate
FL/FR
geraniol
FL/FR
beta-
ionol
FL/FR
alpha-
ionone
FL/FR
beta-
methyl ionone
FL/FR
alpha-iso
methyl ionone (50% min.)
FL/FR
alpha-iso
methyl ionone (70% min.)
FL/FR
(E)-alpha-
methyl ionone (74-80%)
FL/FR
alpha-iso
methyl ionone (80% min.)
FL/FR
alpha-iso
methyl ionone (90% min.)
FL/FR
muguet carbinol
FL/FR
orris rhizome concrete butter (iris pallida)
FL/FR
orris rhizome oil (iris germanica)
FL/FR
orris rhizome resinoid (iris pallida)
FL/FR
violet flower absolute
FL/FR
fruity
benzyl acetate
FL/FR
benzyl formate
FL/FR
boronia absolute
FL/FR
2-
heptanol
FL/FR
methoxymelonal
FL/FR
methyl (E)-2-octenoate
FL/FR
alpha-
methyl ionone
FL/FR
phenethyl isovalerate
FL/FR
star fruit oil cuba
FL/FR
green
dibutyl sulfide
FL/FR
(Z)-3-
hexen-1-yl (Z)-3-hexenoate
FL/FR
(Z)-3-
hexen-1-yl methyl carbonate
FL/FR
(Z)-
leaf acetal
FL/FR
melon nonenoate
FL/FR
methyl heptine carbonate
FL/FR
methyl octine carbonate
FL/FR
3,6-
nonadien-1-ol
FL/FR
(E,Z)-2,6-
nonadienal
FL/FR
(E)-2-
nonen-1-ol
FL/FR
octanal dimethyl acetal
FL/FR
violet leaf absolute
FL/FR
honey
phenethyl isobutyrate
FL/FR
solvent
1-
heptanol
FL/FR
spicy
benzyl cinnamate
FL/FR
cassie absolute
FL/FR
sweet
orris rhizome absolute (iris germanica)
FL/FR
orris rhizome absolute (iris pallida)
FL/FR
saffron resinoid
FL/FR
tropical
alpha-
amyl cinnamaldehyde
FL/FR
3-
mercaptohexyl acetate
FL/FR
waxy
butyl undecylenate
FL/FR
ethyl myristate
FL/FR
woody
alpha-
ionol
FL/FR
beta-
ionyl acetate
FL/FR
alpha-
irone
FL/FR
methyl ionyl acetate
FL/FR
orris rhizome oil CO2 extract
FL/FR
 
Potential Uses:
FRfloral
FRmoss
FRoriental
FRviolet
FRwoody
 
Occurrence (nature, food, other):note
 not found in nature
 
Synonyms:
 cyclohexanepropanol, a,2,2,6-tetramethyl-
 tetrahydroional
 tetrahydroionol
alpha,2,2,6-tetramethyl cyclohexane propanol
4-(2,2,6-trimethylcyclohexyl)butan-2-ol
 
 
Notes:
None found
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