para-tert-butyl quinoline
quinoline, (1,1-dimethylethyl)-
 
Notes:
None found
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5-tert-butylquinoline (Click)
CAS Number: 61702-91-8Picture of molecule
ECHA EINECS - REACH Pre-Reg: 262-927-9
Nikkaji Web: J561.524K
XlogP3-AA: 3.90 (est)
Molecular Weight: 185.26955000
Formula: C13 H15 N
NMR Predictor: Predict (works with chrome or firefox)
Category: fragrance agents
 
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Physical Properties:
Appearance: yellow to dark brown clear liquid (est)
Assay: 97.00 to 100.00 % 
Food Chemicals Codex Listed: No
Boiling Point: 286.00 to  287.00 °C. @ 760.00 mm Hg
Vapor Pressure: 0.005000 mm/Hg @ 25.00 °C. (est)
Flash Point: > 212.00 °F. TCC ( > 100.00 °C. )
logP (o/w): 3.741 (est)
Soluble in:
 alcohol
 water, 17.97 mg/L @ 25 °C (est)
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Organoleptic Properties:
Odor Type: animal
Odor Strength: high ,
recommend smelling in a 1.00 % solution or less
 castoreum  leathery  earthy  oakmoss  vetiver  
Odor Description:
at 100.00 %. 
castoreum leather earthy oakmoss vetiver
  
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Cosmetic Information:
CosIng: cosmetic data
Cosmetic Uses: perfuming agents
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Suppliers:
CG Herbals
para-tert-Butyl Quinoline
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Safety Information:
 
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
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Safety in Use Information:
Category: fragrance agents
Recommendation for para-tert-butyl quinoline usage levels up to:
  1.0000 % in the fragrance concentrate.
 
Recommendation for para-tert-butyl quinoline flavor usage levels up to:
 not for flavor use.
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Safety References:
EPI System: View
EPA Substance Registry Services (TSCA): 61702-91-8
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 109127
National Institute of Allergy and Infectious Diseases: Data
 5-tert-butylquinoline
Chemidplus: 0061702918
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References:
 5-tert-butylquinoline
NIST Chemistry WebBook: Search Inchi
Canada Domestic Sub. List: 61702-91-8
Pubchem (cid): 109127
Pubchem (sid): 135065978
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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: 2933.40.7050
ChemSpider: View
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Potential Blenders and core components note
 
For Odor
No odor group found for these
7-methyl coumarin replacerFR
amber
 ambergris tinctureFL/FR
animal
isobutyl quinolineFR
isobutyl quinolineFR
2-isobutyl quinolineFR
6-tert-butyl-meta-cresolFL/FR
 castoreum extractFL/FR
 castoreum liquidFL/FR
6-methyl quinolineFL/FR
para-methyl tetrahydroquinolineFL/FR
balsamic
 fir balsam absoluteFR
 peru balsam oilFL/FR
 peru balsam resinoidFL/FR
 styrax gum (liquidambar orientalis) 
burnt
 amber oilFR
chocolate
isoamyl phenyl acetateFL/FR
citrus
 tetrahydromyrcenyl acetateFR
floral
alpha-amyl cinnamyl acetateFL/FR
 cananga oilFL/FR
 cananga oil chinaFL/FR
 citronellolFL/FR
 dimethyl octanolFL/FR
 floral methanolFR
 orris pyridine 25% IPMFR
 prenyl salicylateFL/FR
 rhodinol substituesFL/FR
 rose carbonateFR
fruity
 ethyl 3-hydroxyhexanoateFL/FR
 leather propionateFR
 osmanthus flower absoluteFL/FR
 tropical iononeFL/FR
green
(E)-2-hexen-1-yl phenyl acetateFL/FR
 narcissus flower absoluteFR
 oakmoss oilFR
 phenoxyacetaldehyde 50% in benzyl alcoholFR
hay
 hay absoluteFR
 tobacco leaf absoluteFL/FR
herbal
 cananga fruit oilFR
 saffron indenoneFL/FR
 thyme undecaneFR
leathery
2-tert-butyl-6-methyl phenolFR
 castoreum absoluteFL/FR
 leather cyclohexanolFR
marine
green algae absoluteFL/FR
 marine pyridineFR
minty
 peppermint oil terpenesFR
mossy
 flouve oilFR
 oakmoss absoluteFL/FR
 oakmoss absolute replacerFR
 oakmoss phenolFR
 oriental specialtyFR
 sea resorcylateFR
 veramoss (IFF)FR
musty
3-acetyl-2,5-dimethyl furanFL/FR
nutty
2,3-dimethyl pyrazineFL/FR
smoky
 birch tar oilFL/FR
 cade oilFR
alpha-ethoxy-ortho-cresolFL/FR
spicy
 cananga leaf oilFR
beta-caryophyllene alcoholFL/FR
 caryophyllene alcoholFL/FR
 cuminyl alcoholFL/FR
 levisticum officinale root oilFL/FR
4-methyl guaiacolFL/FR
tobacco
3-ethyl pyridineFL/FR
tropical
 genet absoluteFL/FR
waxy
 decanal diethyl acetalFL/FR
woody
para-tert-butyl cyclohexanoneFR
 methyl cedryl ketoneFL/FR
delta-methyl iononeFL/FR
 patchouli hexanolFR
 
For Flavor
 
No flavor group found for these
green algae absoluteFL/FR
 ambergris tinctureFL/FR
 birch tar oilFL/FR
6-tert-butyl-meta-cresolFL/FR
beta-caryophyllene alcoholFL/FR
 caryophyllene alcoholFL/FR
alpha-ethoxy-ortho-cresolFL/FR
 ethyl 3-hydroxyhexanoateFL/FR
(E)-2-hexen-1-yl phenyl acetateFL/FR
 methyl cedryl ketoneFL/FR
delta-methyl iononeFL/FR
6-methyl quinolineFL/FR
para-methyl tetrahydroquinolineFL/FR
 osmanthus flower absoluteFL/FR
 saffron indenoneFL/FR
animal
 castoreum extractFL/FR
 castoreum liquidFL/FR
balsamic
 peru balsam oilFL/FR
 peru balsam resinoidFL/FR
 styrax gum (liquidambar orientalis) 
berry
 rhodinol substituesFL/FR
bitter
 tobacco leaf absoluteFL/FR
caramellic
3-ethyl pyridineFL/FR
earthy
alpha-amyl cinnamyl acetateFL/FR
fatty
 dimethyl octanolFL/FR
floral
isoamyl phenyl acetateFL/FR
 cananga oilFL/FR
 cananga oil chinaFL/FR
 citronellolFL/FR
 tropical iononeFL/FR
green
 oakmoss absoluteFL/FR
hay
 genet absoluteFL/FR
herbal
 prenyl salicylateFL/FR
leathery
 castoreum absoluteFL/FR
musty
2,3-dimethyl pyrazineFL/FR
nutty
3-acetyl-2,5-dimethyl furanFL/FR
spicy
 cuminyl alcoholFL/FR
 levisticum officinale root oilFL/FR
vanilla
4-methyl guaiacolFL/FR
waxy
 decanal diethyl acetalFL/FR
 
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Potential Uses:
 castoreumFR
 oakmoss mousse de chene mossFR
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Natural Occurrence in: note
 not found in nature
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Synonyms:
4-tert-butyl quinoline
p-tert-butyl quinoline
(tert-butyl) quinoline
(tert-butyl)quinoline
4-tert-butylquinoline
5-tert-butylquinoline
p-tert-butylquinoline
p-tertiary-butylquinoline
 quinoline, (1,1-dimethylethyl)-
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