isopropyl quinoline
quinoline, 6-isopropyl-
 
Notes:
Blends well with moss, vetiver and tobacco notes.
  • Berjé
    • Berje Inc.
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      Product(s):
      isoPropyl Quinolene
       
  • BOC Sciences
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      Product(s):
      135-79-5 isoPROPYL QUINOLINE 98.0%
       
  • Lluch Essence
    • Lluch Essence S.L.
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      ISOPROPYLQUINOLEINE
       
  • Moellhausen
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      09-58000 ISOPROPYL QUINOLINE
       
  • TCI AMERICA
    • TCI AMERICA
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      I0529 6-isoPropylquinoline >98.0%(GC)
       
  • Ernesto Ventós
  • Vigon International
    • Vigon International
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      500904 Isopropyl Quinoline
       
Synonyms   Articles   Notes   Search
Fragrance Demo Formulas
CAS Number: 135-79-5Picture of molecule3D/inchi
ECHA EINECS - REACH Pre-Reg: 205-220-2
FDA UNII: 8GE3N8WV7Y
Nikkaji Web: J184.395H
MDL: MFCD00047615
XlogP3: 3.30 (est)
Molecular Weight: 171.24261000
Formula: C12 H13 N
NMR Predictor: Predict (works with chrome, Edge or firefox)
Also(can) Contains: 8-isopropyl quinoline
Category: fragrance agents
 
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Google Scholar: Search
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PubMed: Search
NCBI: Search
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Physical Properties:
Appearance: yellow to brownish yellow liquid (est)
Assay: 98.00 to 100.00 % sum of isomers
Food Chemicals Codex Listed: No
Specific Gravity: 1.01900 to 1.02500 @  25.00 °C.
Pounds per Gallon - (est).: 8.479 to  8.529
Refractive Index: 1.58600 to 1.59300 @  20.00 °C.
Boiling Point: 100.00 °C. @ 0.50 mm Hg
Vapor Pressure: 0.011000 mmHg @ 25.00 °C. (est)
Flash Point: 196.00 °F. TCC ( 91.11 °C. )
logP (o/w): 3.537 (est)
Soluble in:
 alcohol
 water, 287 mg/L @ 20 °C (exp)
Insoluble in:
 water
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Organoleptic Properties:
 
Odor Type: green
 
Odor Strength: high ,
recommend smelling in a 1.00 % solution or less
 
Substantivity: 320 hour(s) at 100.00 %
 
 weedy  green  metallic  earthy  leafy  cortex  phenolic  nutty  
Odor Description:
at 1.00 % in dipropylene glycol. 
weedy green metallic earthy leafy cortex phenolic nutty
Luebke, William tgsc, (1989)
 
Odor and/or flavor descriptions from others (if found).
 
Bedoukian Research
ISOPROPYL QUINOLINE ≥98.0%, Kosher
Odor Description: vegetable leaf, earthy green
Used in fragrances, soaps and lotions.
 
Givaudan
Isopropyl Quinoline
Odor Description: Leather, Woody, Moss
Isopropyl Quinoline is an indispensable element in the formulation of masculine notes, where it blends very well with mossy vetiver, chypre and tobacco accords, as well as with animal and spicy types. It is a rich and vibrant material which leads to great originality in compounds. Its influence is constant throughout the evaporation of a fragrance and gives volume, strength and diffusion.
 
 
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Cosmetic Information:
CosIng: cosmetic data
Cosmetic Uses: perfuming agents
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Suppliers:
Berjé
isoPropyl Quinolene
Media
BOC Sciences
For experimental / research use only.
isoPROPYL QUINOLINE 98.0%
Ernesto Ventós
ISOPROPYLQUINOLINE
Givaudan
Isopropyl Quinoline
Odor: Leather, Woody, Moss
Use: Isopropyl Quinoline is an indispensable element in the formulation of masculine notes, where it blends very well with mossy vetiver, chypre and tobacco accords, as well as with animal and spicy types. It is a rich and vibrant material which leads to great originality in compounds. Its influence is constant throughout the evaporation of a fragrance and gives volume, strength and diffusion.
Lluch Essence
ISOPROPYLQUINOLEINE
Moellhausen
6-ISOPROPYL QUINOLINE (80/20)
Moellhausen
6-ISOPROPYL QUINOLINE 98%
Penta International
ISOPROPYL QUINOLINE
Santa Cruz Biotechnology
For experimental / research use only.
6-isoPropylquinoline
TCI AMERICA
For experimental / research use only.
6-isoPropylquinoline >98.0%(GC)
Vigon International
Isopropyl Quinoline
Odor: EARTHY, WOODY, ROOT-LIKE
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Safety Information:
Preferred SDS: View
European information :
Most important hazard(s):
T - Toxic.
R 22 - Harmful if swallowed.
R 24 - Toxic in contact with skin.
R 38 - Irritating to skin.
S 02 - Keep out of the reach of children.
S 20/21 - When using do not eat, drink or smoke.
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  940 mg/kg
Food and Cosmetics Toxicology. Vol. 13, Pg. 821, 1975.

Dermal Toxicity:
skin-rabbit LD50 160 mg/kg
Food and Cosmetics Toxicology. Vol. 13, Pg. 821, 1975.

Inhalation Toxicity:
Not determined
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Safety in Use Information:
Category: fragrance agents
RIFM Fragrance Material Safety Assessment: Search
IFRA Code of Practice Notification of the 49th Amendment to the IFRA Code of Practice
Recommendation for isopropyl quinoline usage levels up to:
  2.0000 % in the fragrance concentrate.
 
Recommendation for isopropyl quinoline flavor usage levels up to:
 not for flavor use.
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Safety References:
EPI System: View
AIDS Citations: Search
Cancer Citations: Search
Toxicology Citations: Search
EPA Substance Registry Services (TSCA): 135-79-5
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 67285
National Institute of Allergy and Infectious Diseases: Data
WISER: UN 2810
WGK Germany: 3
 6-propan-2-ylquinoline
Chemidplus: 0000135795
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References:
 6-propan-2-ylquinoline
NIST Chemistry WebBook: Search Inchi
Canada Domestic Sub. List: 135-79-5
Pubchem (cid): 67285
Pubchem (sid): 135025803
Pherobase: View
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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
CHEMBL: View
HMDB (The Human Metabolome Database): Search
Export Tariff Code: 2933.49.7000
ChemSpider: View
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Potential Blenders and core components note
 
For Odor
aldehydic
 fresh carbaldehydeFR
 green hexanalFL/FR
alliaceous
 dipropyl disulfideFL/FR
balsamic
 bornyl formateFL/FR
 hemlock western oil (tsuga heterophylla) canadaFR
 propyl cinnamateFL/FR
 spruce needle absoluteFL/FR
 tetrahydrofurfuryl cinnamateFL/FR
 neroli ketoneFR
 petitgrain combava oilFR
coconut
delta-heptalactoneFL/FR
earthy
1-nonen-3-olFL/FR
scotch pine needle oilFL/FR
scotch pine needle oil estoniaFL/FR
scotch pine needle oil yugoslaviaFL/FR
ethereal
 ethyl acetateFL/FR
fatty
5-methyl-5-hexen-2-oneFL/FR
(E)-2-octenalFL/FR
(Z)-2-octenal 
floral
 allyl anthranilateFL/FR
 anisyl propanal / methyl anthranilate schiff's baseFR
 cassie absoluteFL/FR
 cassie concreteFR
 dimethyl benzyl carbinolFL/FR
2,4-dimethyl cyclohexyl methyl acetateFR
 gardenia oxideFR
 geranium oil africaFL/FR
(Z)-3-hexen-1-yl salicylateFL/FR
 hyacinth etherFR
 ocean propanal / methyl anthranilate schiff's baseFR
 octyl acetateFL/FR
bitter orangeflower absolute moroccoFL/FR
 phenethyl butyl etherFR
 phenyl acetaldehyde diisobutyl acetalFL/FR
2-phenyl propyl acetateFL/FR
isopropyl phenyl acetateFL/FR
 rose absolute (rosa damascena) bulgariaFL/FR
laevo-rose oxideFL/FR
 styralyl propionateFL/FR
fruity
 amyl formateFL/FR
 ethyl 3-hexenoateFL/FR
(E)-2-hexen-1-olFL/FR
2-hexen-1-olFL/FR
2-nonanoneFL/FR
2-pentyl furanFL/FR
green
 acetaldehyde butyl phenethyl acetalFL/FR
 acetaldehyde di-(Z)-3-hexen-1-yl acetalFL/FR
 acetaldehyde ethyl phenethyl acetalFL/FR
 benzhydrolFR
2-isobutyl thiazoleFL/FR
 cumin acetaldehydeFL/FR
3,5,6-neocyclocitralFR
 galbanum absolute replacerFR
 galbanum oil terpenelessFL/FR
 geranium absoluteFL/FR
 green etherFL/FR
isogreen methanoindeneFR
 green specialtyFR
1-hepten-3-olFL/FR
 heptyl cinnamateFL/FR
3-hexen-1-olFL/FR
(Z)-2-hexen-1-olFL/FR
(E)-2-hexen-1-yl acetateFL/FR
(Z)-3-hexen-1-yl benzoateFL/FR
(Z)-3-hexen-1-yl lactateFL/FR
(Z)-3-hexen-1-yl methyl carbonateFL/FR
(Z)-3-hexen-1-yl octanoateFL/FR
(Z)-3-hexen-1-yl tiglateFL/FR
3-hexenalFL/FR
 hexoxyacetaldehyde dimethyl acetalFR
2,4-ivy carbaldehydeFL/FR
3,6-ivy carbaldehydeFL/FR
 ivy carbaldehydeFL/FR
3,5-ivy carbaldehydeFL/FR
2,4-ivy carbaldehyde / methyl anthranilate schiff's baseFR
 ivy dioxolaneFR
(Z)-leaf acetalFL/FR
 leafy acetalFL/FR
 leafy oximeFR
 methyl heptine carbonateFL/FR
 narcissus flower absoluteFR
 nerol oxideFL/FR
(E,Z)-2,6-nonadien-1-yl acetateFL/FR
 octanal dimethyl acetalFL/FR
(Z)-5-octen-1-yl propionateFL/FR
 phenethyl acetalFR
 phenoxyacetaldehyde 50% in benzyl alcoholFR
3-phenyl propionaldehydeFL/FR
1-phenyl-2-pentanolFL/FR
 pineapple heptadienone 10%FR
isopropyl phenyl propionaldehydeFR
4-isopropyl quinolineFL/FR
 rose leaf absolute (rosa centifolia)FL/FR
 styralyl acetateFL/FR
3,5,5-trimethyl hexanolFL/FR
 triplal / ethyl anthranilate schiff's baseFR
herbal
sweet basil absoluteFL/FR
 herbal heptaneFR
 herbal ketoneFR
 lovage tinctureFL/FR
 rosemary oleoresinFL/FR
minty
isopulegyl formateFL/FR
sulfurous
 cassis pentanoneFL/FR
waxy
 allyl nonanoateFL/FR
 octyl isobutyrateFL/FR
woody
1,3,5,7-undecatetraeneFL/FR
 
For Flavor
 
No flavor group found for these
 acetaldehyde di-(Z)-3-hexen-1-yl acetalFL/FR
 allyl anthranilateFL/FR
 bornyl formateFL/FR
 epoxy-2-decenalFL
 heptyl cinnamateFL/FR
3-hexen-1-olFL/FR
2-hexenalFL
(E)-2-hexenalFL
 ivy carbaldehydeFL/FR
3,5-ivy carbaldehydeFL/FR
3-methyl-3-pentanolFL
(Z)-2-octenal 
2-phenyl propyl acetateFL/FR
scotch pine needle oilFL/FR
scotch pine needle oil estoniaFL/FR
scotch pine needle oil yugoslaviaFL/FR
2-isopropyl pyridineFL
3-propyl pyridineFL
4-isopropyl quinolineFL/FR
isopulegyl formateFL/FR
 tetrahydrofurfuryl cinnamateFL/FR
1,3,5,7-undecatetraeneFL/FR
alliaceous
 dipropyl disulfideFL/FR
aromatic
 leafy acetalFL/FR
balsamic
 spruce needle absoluteFL/FR
2-nonanoneFL/FR
citrus
 styralyl propionateFL/FR
creamy
 octyl isobutyrateFL/FR
earthy
1-nonen-3-olFL/FR
ethereal
 ethyl acetateFL/FR
5-methyl-5-hexen-2-oneFL/FR
fatty
(Z)-3-hexen-1-yl benzoateFL/FR
(E)-2-octenalFL/FR
floral
 geranium oil africaFL/FR
bitter orangeflower absolute moroccoFL/FR
 rose absolute (rosa damascena) bulgariaFL/FR
laevo-rose oxideFL/FR
fruity
 amyl formateFL/FR
 ethyl 3-hexenoateFL/FR
2-hexen-1-olFL/FR
1-phenyl-2-pentanolFL/FR
 propyl cinnamateFL/FR
 styralyl acetateFL/FR
green
 acetaldehyde butyl phenethyl acetalFL/FR
 acetaldehyde ethyl phenethyl acetalFL/FR
2-isobutyl thiazoleFL/FR
 cassis pentanoneFL/FR
 cumin acetaldehydeFL/FR
 galbanum oil terpenelessFL/FR
 geranium absoluteFL/FR
 green etherFL/FR
1-hepten-3-olFL/FR
(E)-2-hexen-1-olFL/FR
(Z)-2-hexen-1-olFL/FR
(E)-2-hexen-1-yl acetateFL/FR
(Z)-3-hexen-1-yl lactateFL/FR
(Z)-3-hexen-1-yl methyl carbonateFL/FR
(Z)-3-hexen-1-yl octanoateFL/FR
(Z)-3-hexen-1-yl salicylateFL/FR
(Z)-3-hexen-1-yl tiglateFL/FR
3-hexenalFL/FR
2,4-ivy carbaldehydeFL/FR
3,6-ivy carbaldehydeFL/FR
(Z)-leaf acetalFL/FR
 methyl heptine carbonateFL/FR
 nerol oxideFL/FR
(E,Z)-2,6-nonadien-1-yl acetateFL/FR
 octanal dimethyl acetalFL/FR
(Z)-5-octen-1-yl propionateFL/FR
2-pentyl furanFL/FR
 phenyl acetaldehyde diisobutyl acetalFL/FR
3-phenyl propionaldehydeFL/FR
 rose leaf absolute (rosa centifolia)FL/FR
3,5,5-trimethyl hexanolFL/FR
herbal
sweet basil absoluteFL/FR
 green hexanalFL/FR
 lovage tinctureFL/FR
 rosemary oleoresinFL/FR
honey
isopropyl phenyl acetateFL/FR
lactonic
delta-heptalactoneFL/FR
medicinal
 dimethyl benzyl carbinolFL/FR
onion
 methyl propyl trisulfideFL
spicy
 cassie absoluteFL/FR
sulfurous
 methyl benzyl disulfideFL
vegetable
alpha-benzylidene methionalFL
waxy
 allyl nonanoateFL/FR
 octyl acetateFL/FR
 
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Potential Uses:
 castoreumFR
 chypreFR
 cortexFR
 earthFR
 fernFR
 greenFR
 leaf 
 metallic 
 mossFR
 orchidFR
 smokeFR
 tobaccoFR
 vetiverFR
 weedy 
 woodyFR
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Occurrence (nature, food, other): note
 not found in nature
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Synonyms:
 base 3
6-(methylethyl)quinoline
6-(propan-2-yl)quinoline
6-propan-2-ylquinoline
isopropyl quinolene
6-isopropyl quinoline
6(8)-isopropyl quinoline
6-isopropyl quinoline (8020)
8-(isopropyl) quinoline
6-(isopropyl)quinoline
6-isopropylquinoline
 quinoline, 6-(1-methylethyl)-
 quinoline, 6-isopropyl-
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