Identification

Namepatchouli hexanol
IUPAC4-tert-butylcyclohexan-1-ol
CAS Number98-52-2
EINECS202-676-4
FDA UNIIK0H1405S9C
Molecular FormulaC10 H20 O
Molecular Weight156.26860000
MDL NumberMFCD00001473
Nikkaji NumberJ23.542C
Beilstein1902277
XlogP33.00 (est)

Regulatory

Physical Properties

Appearance white solid (est)
Assay 98.00 to 100.00 sum of isomers
Food Chemicals Codex Listed No
Melting Point 65.00 to 70.00 °C. @ 760.00 mm Hg
Boiling Point 110.00 to 115.00 °C. @ 15.00 mm Hg
Vapor Pressure 0.035000 mmHg @ 25.00 °C. (est)
Flash Point 221.00 °F. TCC ( 105.00 °C. )
logP (o/w) 3.092 (est)
Shelf Life 36.00 month(s) or longer if stored properly.
Storage store in cool, dry place in tightly sealed containers, protected from heat and light.
Soluble in alcohol
Insoluble in water

Cosmetic Information

CosIngcosmetic data
Cosmetic Usesfragrance

Organoleptic Properties

Odor Description
at 100.00 %.
WOODY,PINE,BALSAMIC,CAMPHORACEUOS
Odor sample from Fragrance Resources Inc.

Safety Information

Preferred SDSView
European informationMost important hazard(s):
Oral/Parenteral Toxicityoral-rat LD50 4200 mg/kg
Dermal Toxicityskin-rabbit LD50 > 5000 mg/kg
Inhalation ToxicityNot determined

GHS Classification

['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']

Safety in Use

Categoryfragrance agents
RIFM Fragrance Material Safety AssessmentSearch
Recommendation for patchouli hexanol usage levels up to10.0000 % in the fragrance concentrate.
Recommendation for patchouli hexanol flavor usage levels up tonot for flavor use.

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Berje Inc.

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SRS Aromatics Ltd

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Synerzine, Inc.

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TCI AMERICA

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The John D. Walsh Company, Inc

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Ernesto Ventós S.A.

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Vigon International

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Potential Uses

FR acacia FR amber FR ambergris FR ambreine FR amyris FL/FR angelica FR ash mountain ash FR balsam FR bark FR bayberry FL/FR beech FL/FR benzoin absolute replacer FR bergamot FL/FR birch tar FR bois de rose FR boronia FR boxwood FL buchu leaf FR cabreuva wood FR cade oil replacer FR calamus oil replacer FL/FR camphor tree bark FR cardamom oil replacer FR cedar FR cedar forest FR cedarwood FR cedarwood atlas FR celery FR cigar FL/FR cistus FR citronella FR clary sage oil replacer FR costus FL/FR croton eluteria bark FR cypress oil replacer FR dogwood FR elemi FR fern FR fir needle oil replacer FR forest FR frankincense FL/FR galangal root FR galbanum FR ginger FR gingergrass FL/FR guaiacwood FR gurjun balsam FR hay new mown hay FR heather FR herbal FR hinoki oil replacer FL/FR hyssop FR iris blossom FR juniper FR juniper berry FR labdanum FR mace FR maja FR mimosa FR mint FR oakwood FR opoponax FL/FR orange bitter orange peel FR oregano FR oriental FR orris FR osmanthus FR patchouli FR pine forest FL/FR pine needle FL/FR pine scotch pine FR pinion FR redwood FR sandalwood FR spikenard oil replacer FR spruce FR sweet grass FL/FR tansy oil replacer FL/FR tarragon oil replacer FL tea black tea timber FR tolu balsam FL/FR valerian FR vetiver FR woody FR wormseed oil replacer

Natural Occurrence

not found in nature

Synonyms

p-t- BCH 4-tert- butyl cyclohexanol p-tert- butyl cyclohexanol para-tert- butyl cyclohexanol 4-(tert- butyl)cyclohexan-1-ol 4-tert- butylcyclohexan-1-ol 4-t- butylcyclohexanol 4-tert- butylcyclohexanol p-tert- butylcyclohexanol para-tert- butylcyclohexanol cyclohexanol, 4-(1,1-dimethylethyl)- cyclohexanol, 4-tert-butyl- 4-(1,1- dimethyl ethyl) cyclohexanol 4-(1,1- dimethylethyl)cyclohexanol 4-(2- methyl-2-propanyl)cyclohexanol padaryl patchone (IFF) patchone - PTBCH alcohol patchouli hexanol PTBCH PubMed: Nonivamide, a capsaicin analog, increases dopamine and serotonin release in SH-SY5Y cells via a TRPV1-independent pathway. PubMed: The antimicrobial profile of extracts of a Phormidium-like cyanobacterium changes with phosphate levels. PubMed: Cyclohexanol analogues are positive modulators of GABA(A) receptor currents and act as general anaesthetics in vivo. PubMed: Inhibition of TRPV1 for the treatment of sensitive skin. PubMed: Displacement chromatography on cyclodextrin silicas. IV. Separation of the enantiomers of ibuprofen. PubMed: The metabolism of the isomeric tert.-butylcyclohexanones.