quinoline
1-benzazine
 
Notes:
Alkaloid from various plant spp. incl. Mentha spp.. Also present in cocoa, black tea and scotch whiskey. Flavouring ingredient Quinoline is a heterocyclic aromatic organic compound. It has the formula C9H7N and is a colourless hygroscopic liquid with a strong odour. Aged samples, if exposed to light, become yellow and later brown. Quinoline is only slightly soluble in cold water but dissolves readily in hot water and most organic solvents.; Quinoline is mainly used as a building block to other specialty chemicals. Approximately 4 tonnes are produced annually according to a report published in 2005.[citation needed] Its principal use is as a precursor to 8-hydroxyquinoline, which is a versatile chelating agent and precursor to pesticides. Its 2- and 4-methyl derivatives are precursors to cyanine dyes. Oxidation of quinoline affords quinolinic acid (pyridine-2,3-dicarboxylic acid), a precursor to the herbicide sold under the name "Assert".
  • Charkit Chemical
    • Charkit Chemical Corporation
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      about: Since 1982, Charkit has been committed to expanding the markets we serve as our roster of products and services continues to grow with us. Our substantial portfolio of personal care ingredients now include a wide array of luxury and exotic components to compliment the key products we have always offered. We have expanded our offerings to the nutraceutical, industrial, and resin markets with a growing roster of versatile and unique ingredients. We continue to lead the way in our traditional markets such as Metal and Water Treatment, Imaging, Flavor & Fragrance, Aroma and Food. Our Pharmaceutical offerings continue to expand, still anchored by the Boronic Derivatives that meet the demands of Suzuki coupling reactions. Please contact us to learn how we can help you reach your goals.
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      For over 30 years, Penta Manufacturing Company has played a growing role in worldwide chemistry innovations and applications. As an industry leader, Penta continues to pioneer chemistry-based solutions for practically every area of commerce. Our products and expertise have helped fuel technical advances in dozens of commercial applications including flavoring, coloring, fragrances and chemical processes.
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  • TCI AMERICA
    • TCI AMERICA
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      Q0011 Quinoline >98.0%(GC)(T)
       
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    • Qingdao Free Trade Zone United International Co Ltd
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      7320 Quinoline
       
Synonyms   Articles   Notes   Search
CAS Number: 91-22-5Picture of molecule3D/inchi
ECHA EINECS - REACH Pre-Reg: 202-051-6
FDA UNII: E66400VT9R
Nikkaji Web: J3.922E
Beilstein Number: 0107477
MDL: MFCD00006736
CoE Number: 11364
XlogP3: 2.00 (est)
Molecular Weight: 129.16179000
Formula: C9 H7 N
BioActivity Summary: listing
NMR Predictor: Predict (works with chrome or firefox)
Category: information only not used for fragrances or flavors
 
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
FEMA Number: 3470-VOID
FDA:No longer provide for the use of these seven synthetic flavoring substances
FDA Mainterm (SATF):91-22-5 ; QUINOLINE--NLFG
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Physical Properties:
Appearance: pale yellow to amber clear liquid (est)
Assay: 97.00 to 100.00 % 
Food Chemicals Codex Listed: No
Specific Gravity: 1.09300 to 1.09600 @  20.00 °C.
Pounds per Gallon - (est).: 9.105 to  9.130
Refractive Index: 1.62400 to 1.62800 @  20.00 °C.
Melting Point: -16.00 to  -14.00 °C. @ 760.00 mm Hg
Boiling Point: 113.00 to  114.00 °C. @ 17.00 mm Hg
Boiling Point: 236.00 to  237.00 °C. @ 760.00 mm Hg
Vapor Pressure: 0.082000 mmHg @ 25.00 °C. (est)
Vapor Density: 4.5 ( Air = 1 )
Flash Point: 214.00 °F. TCC ( 101.11 °C. )
logP (o/w): 2.030
Soluble in:
 alcohol
 water, 1711 mg/L @ 25 °C (est)
 water, 6110 mg/L @ 25 °C (exp)
Insoluble in:
 water
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Organoleptic Properties:
 
Odor Type: medicinal
 
 medicinal  musty  tobacco  rubbery  earthy  
Odor Description:
at 1.00 % in triacetin. 
medical musty tobacco rubber earthy
 
 medicinal  musty  tobacco  leathery  
Odor Description:
at 1.00 %.  
Medical, musty, tobacco with a pyridine and leather nuance
Mosciano, Gerard P&F 26, No. 2, 40, (2001)
 
 
Flavor Type: earthy
 
 earthy  musty  nutty  coumarinic  chemical  
Taste Description:
at 2.00 - 10.00 ppm. 
Earthy, musty, nutty, coumarinic with a chemical nuance
Mosciano, Gerard P&F 26, No. 2, 40, (2001)
 
Odor and/or flavor descriptions from others (if found).
 
 
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Cosmetic Information:
CosIng: cosmetic data
Cosmetic Uses: not used anymore
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Suppliers:
Charkit Chemical
QUINOLINE 96%
Charkit Chemical
QUINOLINE 97.5% STD. GRADE
EMD Millipore
For experimental / research use only.
Quinoline
Penta International
QUINOLINE
Sigma-Aldrich
Quinoline, ≥97%
Certified Food Grade Products
TCI AMERICA
For experimental / research use only.
Quinoline >98.0%(GC)(T)
United International
Quinoline
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Safety Information:
Preferred SDS: View
European information :
Most important hazard(s):
Xn - Harmful.
R 21/22 - Harmful in contact with skin and if swallowed.
R 37/38 - Irritating to respiratory system and skin.
R 41 - Risk of serious damage to eyes.
S 02 - Keep out of the reach of children.
S 20/21 - When using do not eat, drink or smoke.
S 23 - Do not breath vapour.
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  331 mg/kg
"Prehled Prumyslove Toxikologie; Organicke Latky," Marhold, J., Prague, Czechoslovakia, Avicenum, 1986Vol. -, Pg. 848, 1986.

Dermal Toxicity:
skin-rabbit LD50 540 ul/kg
AMA Archives of Industrial Hygiene and Occupational Medicine. Vol. 4, Pg. 119, 1951.

subcutaneous-rabbit LD50 200 mg/kg
"Abdernalden's Handbuch der Biologischen Arbeitsmethoden." Vol. 4, Pg. 1289, 1935.

Inhalation Toxicity:
Not determined
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Safety in Use Information:
Category: information only not used for fragrances or flavors
IFRA Critical Effect: Carcinogenicity, mutagenicity
IFRA: View Standard
Recommendation for quinoline usage levels up to:
 PROHIBITED: Should not be used as a fragrance ingredient.
 
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
publication number: 9
Click here to view publication 9
 average usual ppmaverage maximum ppm
baked goods: -3.00000
beverages(nonalcoholic): -1.00000
beverages(alcoholic): --
breakfast cereal: --
cheese: --
chewing gum: --
condiments / relishes: --
confectionery froastings: -3.00000
egg products: --
fats / oils: --
fish products: --
frozen dairy: -2.50000
fruit ices: -2.50000
gelatins / puddings: -2.50000
granulated sugar: --
gravies: -2.50000
hard candy: --
imitation dairy: --
instant coffee / tea: --
jams / jellies: --
meat products: -2.50000
milk products: --
nut products: --
other grains: --
poultry: --
processed fruits: --
processed vegetables: --
reconstituted vegetables: --
seasonings / flavors: --
snack foods: --
soft candy: --
soups: -2.50000
sugar substitutes: --
sweet sauces: --
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Safety References:
EPI System: View
EPA-Iris: IRIS
NIOSH International Chemical Safety Cards: search
Chemical Carcinogenesis Research Information System: Search
AIDS Citations: Search
Cancer Citations: Search
Toxicology Citations: Search
EPA GENetic TOXicology: Search
EPA Substance Registry Services (TSCA): 91-22-5
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 7047
National Institute of Allergy and Infectious Diseases: Data
WISER: UN 2656
WGK Germany: 2
 quinoline
Chemidplus: 0000091225
EPA/NOAA CAMEO: hazardous materials
RTECS: 91-22-5
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References:
 quinoline
NIST Chemistry WebBook: Search Inchi
Canada Domestic Sub. List: 91-22-5
Pubchem (cid): 7047
Pubchem (sid): 134971443
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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
FDA Substances Added to Food (formerly EAFUS): View
CHEBI: View
CHEMBL: View
KEGG (GenomeNet): C06413
HMDB (The Human Metabolome Database): HMDB33731
FooDB: FDB011854
Export Tariff Code: 2933.49.7000
VCF-Online: VCF Volatile Compounds in Food
ChemSpider: View
Wikipedia: View
Formulations/Preparations:
•grades: reagent; technical •commercial quinoline is at least 90% pure. chromatographic composition of this product is typically 92% quinoline and 5% isoquinoline by weight.
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Potential Blenders and core components note
 
For Odor
amber
amber
 ambrette seed absoluteFL/FR
animal
2-isobutyl quinolineFR
isobutyl quinolineFR
isobutyl quinolineFR
6-methyl quinolineFL/FR
balsamic
 amyl phenyl acetateFL/FR
isobornyl formateFL/FR
burnt
 amber oilFR
cereal
 bran absoluteFR
earthy
 geosminFL/FR
1-octen-3-oneFL/FR
floral
alpha-amyl cinnamyl acetateFL/FR
 boronia butenalFR
 cananga oilFL/FR
 cananga oil chinaFL/FR
 citronellolFL/FR
delta-damasconeFL/FR
 dimethyl octanolFL/FR
 floral methanolFR
2-methyl-4-phenyl butanalFL/FR
 orris pyridine 25% IPMFR
 rhodinol substituesFL/FR
 tobacco flower absoluteFR
fruity
alpha-amyl cinnamyl isovalerateFL/FR
 cyclohexanone diethyl acetalFL/FR
beta-damasconeFL/FR
(E)-beta-damasconeFL/FR
(Z)-beta-damasconeFL/FR
 ethyl 3-hydroxyhexanoateFL/FR
 leather propionateFR
 osmanthus flower absoluteFL/FR
fungal
 methyl 2-furoateFL/FR
green
 phenoxyacetaldehyde 50% in benzyl alcoholFR
hay
 beeswax absoluteFL/FR
 hay absoluteFR
 tobacco leaf absoluteFL/FR
 woodruff absoluteFR
 matricaria chamomilla flower oilFL/FR
 methyl nicotinateFL/FR
 saffron indenoneFL/FR
 safranalFL/FR
 theaspiraneFL/FR
 thyme undecaneFR
 yerba mate absoluteFL/FR
honey
 phenyl acetic acidFL/FR
leathery
4-tert-butyl phenolCS
 castoreum absoluteFL/FR
 leather cyclohexanolFR
marine
 marine pyridineFR
mossy
 oakmoss absoluteFL/FR
musty
ketoisophoroneFL/FR
nutty
2,3-dimethyl pyrazineFL/FR
2,3,5-trimethyl pyrazineFL/FR
phenolic
meta-cresolFR
2'-hydroxyacetophenoneFL/FR
popcorn
2-acetyl pyridineFL/FR
4-carvomenthenolFL/FR
 cuminyl alcoholFL/FR
N,N-diethyl octanamideFR
 ginger oleoresinFL/FR
4-methyl guaiacolFL/FR
tobacco
para-cresyl isovalerateFL/FR
3-ethyl pyridineFL/FR
 methyl benzoxoleFL/FR
 tobacco concreteFR
(E,E/E,Z)-tobacco cyclohexenoneFL/FR
 veltonal (Bedoukian)FR
tonka
 deertongue absoluteFR
gamma-hexalactoneFL/FR
 mint lactoneFL/FR
 saffron resinoidFL/FR
 tonka undecanoneFR
tropical
 genet absoluteFL/FR
vanilla
 propenyl guaetholFL/FR
woody
 amber decatrieneFR
alpha-cedrene epoxideFR
isolongifolene ketoneFR
 methyl cedryl ketoneFL/FR
 tobacarol (IFF)FR
 tobacco noneneFR
 woody dioxolaneFR
 woody etherFR
 
For Flavor
 
No flavor group found for these
 amyl phenyl acetateFL/FR
 butyraldehyde sulfidedFL
 capsicum oleoresinFL
 cyclohexanone diethyl acetalFL/FR
2,6-dimethoxy-4-vinyl phenolFL
 fig leaf absoluteFL
2-furfurylidene butyraldehydeFL
 geosminFL/FR
 methyl nicotinateFL/FR
2-methyl-4-phenyl butanalFL/FR
2-propyl pyridineFL
beta-damasconeFL/FR
animal
6-methyl quinolineFL/FR
berry
 rhodinol substituesFL/FR
brown
 beeswax absoluteFL/FR
caramellic
3-ethyl pyridineFL/FR
 methyl 2-furoateFL/FR
citrus
ketoisophoroneFL/FR
cooling
4-carvomenthenolFL/FR
 theaspiraneFL/FR
corn
2-acetyl pyridineFL/FR
creamy
gamma-hexalactoneFL/FR
 mint lactoneFL/FR
earthy
alpha-amyl cinnamyl acetateFL/FR
1-octen-3-oneFL/FR
fatty
 dimethyl octanolFL/FR
floral
 cananga oilFL/FR
 cananga oil chinaFL/FR
 citronellolFL/FR
 phenyl acetic acidFL/FR
fruity
alpha-amyl cinnamyl isovalerateFL/FR
(E)-beta-damasconeFL/FR
(Z)-beta-damasconeFL/FR
 ethyl 3-hydroxyhexanoateFL/FR
 osmanthus flower absoluteFL/FR
grassy
 tobacco leaf absoluteFL/FR
green
 oakmoss absoluteFL/FR
isophoroneFL
hay
 genet absoluteFL/FR
herbal
 matricaria chamomilla flower oilFL/FR
 saffron indenoneFL/FR
 yerba mate absoluteFL/FR
leathery
 castoreum absoluteFL/FR
musty
2,3,5-trimethyl pyrazineFL/FR
naphthyl
2'-hydroxyacetophenoneFL/FR
nutty
2,3-dimethyl pyrazineFL/FR
 methyl benzoxoleFL/FR
(E,E/E,Z)-tobacco cyclohexenoneFL/FR
phenolic
para-cresyl isovalerateFL/FR
spicy
 cuminyl alcoholFL/FR
 ginger oleoresinFL/FR
4-methyl guaiacolFL/FR
 paprika oleoresinFL
sweet
 saffron resinoidFL/FR
vanilla
 propenyl guaetholFL/FR
woody
 ambrette seed absoluteFL/FR
isobornyl formateFL/FR
delta-damasconeFL/FR
 methyl cedryl ketoneFL/FR
 safranalFL/FR
 
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Potential Uses:
 cherryFL
 chocolate cocoaFL
 coffeeFL
 fishFL
 hazelnutFL
 lobsterFL
 potatoFL
 seafoodFL
 prawnFL
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Occurrence (nature, food, other): note
 bonito dried bonito
Search  PMC Picture
 cocoa
Search Trop  Picture
 coffee
Search  PMC Picture
 fig leaf
Search Trop  Picture
 rice cooked rice
Search  PMC Picture
 tea black tea
Search Trop  Picture
 tea plant
Search Trop  Picture
 tobacco burley
Search  Picture
 whiskey scotch whiskey
Search  Picture
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Synonyms:
1-benzazine
1-benzine
 benzo(b)pyridine
 benzo[b]pyridine
 benzopyridine
2,3-benzopyridine
 chinoleine
 chinolin
 leucol
 leukol
1-azanaphthalene
 quinolin
 quinoline pure
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