ChemicalBook > CAS DataBase List > 6-Methylquinoline

6-Methylquinoline

Product Name
6-Methylquinoline
CAS No.
91-62-3
Chemical Name
6-Methylquinoline
Synonyms
7-bromo-6-chloroquinazolin-4(3H)-one;PARA METHYL QUINOLINE;FEMA 2744;P-TOLUQUINOLINE;6-methyquinoline;6-Methylchinolin;6-METHYLQUINOLINE;p-Methylquinoline;6-methyl-quinolin;6-Methylquinoline50
CBNumber
CB9138173
Molecular Formula
C10H9N
Formula Weight
143.19
MOL File
91-62-3.mol
More
Less

6-Methylquinoline Property

Melting point:
-22°C
Boiling point:
256-260 °C (lit.)
Density 
1.067 g/mL at 20 °C (lit.)
vapor density 
>1 (vs air)
refractive index 
n20/D 1.614(lit.)
FEMA 
2744 | 6-METHYLQUINOLINE
Flash point:
>230 °F
storage temp. 
Store below +30°C.
solubility 
Chloroform (Slightly), Methanol (Slightly), soluble in alcohol and oils, and in Propylene glycol.
form 
Liquid
pka
5.21±0.10(Predicted)
color 
green-yellow
Specific Gravity
1.07
Odor
blossom odor, sweet, animalic upon dilution
Odor Type
animal
Water Solubility 
Not miscible or difficult to mix with water.
Sensitive 
Light Sensitive
JECFA Number
1302
BRN 
110336
LogP
2.54
CAS DataBase Reference
91-62-3(CAS DataBase Reference)
NIST Chemistry Reference
Quinoline, 6-methyl-(91-62-3)
EPA Substance Registry System
6-Methylquinoline (91-62-3)
More
Less

Safety

Hazard Codes 
Xn
Risk Statements 
22-38-68-36/37/38
Safety Statements 
26-36-45-36/37/39
WGK Germany 
3
RTECS 
VC0550000
TSCA 
Yes
HS Code 
29334990
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

H315Causes skin irritation

Precautionary statements

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P270Do not eat, drink or smoke when using this product.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P301+P312IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P332+P313IF SKIN irritation occurs: Get medical advice/attention.

More
Less

N-Bromosuccinimide Price

Sigma-Aldrich
Product number
108928
Product name
6-Methylquinoline
Purity
98%
Packaging
25g
Price
$94.1
Updated
2024/03/01
Sigma-Aldrich
Product number
108928
Product name
6-Methylquinoline
Purity
98%
Packaging
100g
Price
$180
Updated
2024/03/01
TCI Chemical
Product number
M0416
Product name
6-Methylquinoline
Purity
>98.0%(GC)(T)
Packaging
5g
Price
$23
Updated
2024/03/01
TCI Chemical
Product number
M0416
Product name
6-Methylquinoline
Purity
>98.0%(GC)(T)
Packaging
25g
Price
$68
Updated
2024/03/01
Alfa Aesar
Product number
B21892
Product name
6-Methylquinoline, 98%
Packaging
5g
Price
$18.65
Updated
2024/03/01
More
Less

6-Methylquinoline Chemical Properties,Usage,Production

Chemical Properties

6-Methylquinoline is a clear light yellow to light orange liquid that has a pungent, heavy odor. dissolved in 4 volumes of 50% ethanol or 60% ethanol of the same volume and in oily fragrances. May be synthesized from p-amino-benzaldehyde and acetone.

Occurrence

Reported found in Finnish and Japanese whiskey.

Application

6-Methylquinoline, is a building block used for the synthesis of various pharmaceutical compounds, and biologically active compounds. It can be used for the preparation of pyranobenzopyrone compounds, having anti-norovirus activity.

Uses

6-Methylquinoline can be used as primary carbon source in culture of Pseudomonas putida QP1. 6-Methylquinoline was used in the synthesis of fluorescent halide-sensitive quinolinium dyes and fluorescent probes for determination of chloride in biological systems.

Definition

ChEBI: 6-methylquinoline is a member of quinolines.

General Description

Clear pale yellow liquid or oil with a quinoline odor.

Air & Water Reactions

Insoluble in water.

Reactivity Profile

6-Methylquinoline is sensitive to prolonged exposure to light. May react vigorously with strong oxidizing agents and strong acids . Neutralizes acids in exothermic reactions to form salts plus water. May be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. Flammable gaseous hydrogen may be generated in combination with strong reducing agents, such as hydrides.

Fire Hazard

6-Methylquinoline is probably combustible.

Biochem/physiol Actions

6-Methylquinoline undergoes biodegradation by quinoline-degrading culture of Pseudomonas putida.

Synthesis

6-Methylquinoline is obtain from coal tar, by synthesis from p-aminobenzaldehyde and acetone.

Purification Methods

Reflux it with BaO, then fractionally distil it. Further purified it via its recrystallised ZnCl2 complex (m 190o). [Cumper et al. J Chem Soc 1176 1962, Beilstein 20 III/IV 3498, 20/7 V 400.]

6-Methylquinoline Preparation Products And Raw materials

Raw materials

Preparation Products

More
Less

6-Methylquinoline Suppliers

HBCChem, Inc.
Tel
+1-510-219-6317
Fax
+1-650-486-1361
Email
sales@hbcchem.com
Country
United States
ProdList
10648
Advantage
60
Alchem Pharmtech,Inc.
Tel
8485655694
Email
sales@alchempharmtech.com
Country
United States
ProdList
63687
Advantage
58
Aladdin Scientific
Tel
+1-+1(833)-552-7181
Email
sales@aladdinsci.com
Country
United States
ProdList
57505
Advantage
58
Abblis Chemicals LLC
Tel
--
Fax
--
Email
info@abblis.com
Country
United States
ProdList
1272
Advantage
0
Alfa Chemistry
Tel
--
Fax
--
Email
info@Alfa-Chemistry.com
Country
United States
ProdList
6814
Advantage
0
SLN Pharmachem
Tel
--
Fax
--
Email
slnpharmachem@vsnl.net
Country
United States
ProdList
188
Advantage
43
Panslavia Chemicals, LLC
Tel
--
Fax
--
Country
United States
ProdList
310
Advantage
50
Rintech, Inc.
Tel
--
Fax
--
Email
info@rintechinc.com
Country
United States
ProdList
3416
Advantage
60
Panslavia Chemicals
Tel
--
Fax
--
Country
United States
ProdList
121
Advantage
58
Synerzine, Inc. (formerly Pyrazine Specialties and CTC Organics)
Tel
--
Fax
--
Email
info@synerzine.com
Country
United States
ProdList
270
Advantage
58
Wilshire Technologies, Inc.
Tel
--
Fax
--
Email
info@wilshiretechnologies.com
Country
United States
ProdList
893
Advantage
58
Wilshire Technologies
Tel
--
Fax
--
Country
United States
ProdList
428
Advantage
58
Frutarom (F&F Ingredients)
Tel
--
Fax
--
Email
info@frutarom.com
Country
United States
ProdList
280
Advantage
58
Admiral Chemicals LLC
Tel
--
Fax
--
Email
office@admiralchemicals.com
Country
United States
ProdList
49
Advantage
58
Penta Manufacturing Company (a division of Penta International Corporation)
Tel
--
Fax
--
Email
@pentamfg.com
Country
United States
ProdList
901
Advantage
58
Fine Chem Trading LTD
Tel
--
Fax
--
Email
chemfinder@chemfinder.co.uk
Country
United States
ProdList
1609
Advantage
64
Chiral Management
Tel
--
Fax
--
Email
sales@chiralmanagement.com
Country
United States
ProdList
1332
Advantage
30
CTC Organics, Inc.
Tel
--
Fax
--
Country
United States
ProdList
95
Advantage
58
Augustus Oils Ltd
Tel
--
Fax
--
Email
essentials@augustus-oils.ltd.uk
Country
United States
ProdList
1404
Advantage
58
Lluch Essence S.L.
Tel
--
Fax
--
Email
web@lluche.com
Country
United States
ProdList
2352
Advantage
58
OQEMA
Tel
--
Fax
--
Email
fandf@oqema.co.uk
Country
United States
ProdList
578
Advantage
58
Indukern, S.A. F&F Ingredients Division
Tel
--
Fax
--
Email
info@indukern.es
Country
United States
ProdList
1321
Advantage
58
R C Treatt and Co Ltd
Tel
--
Fax
--
Email
enquiries@treatt.com
Country
United States
ProdList
1690
Advantage
58
Pyrazine Specialties, Inc.
Tel
--
Fax
--
Country
United States
ProdList
1265
Advantage
30
Penta International Corporation
Tel
--
Fax
--
Email
lisaa@pentamfg.com
Country
United States
ProdList
5042
Advantage
58
Moellhausen S.P.A.
Tel
--
Fax
--
Country
United States
ProdList
1676
Advantage
58
TCI America
Tel
--
Fax
--
Email
sales@tciamerica.com
Country
United States
ProdList
6909
Advantage
75
Riedel-de Haen AG
Tel
--
Fax
--
Country
United States
ProdList
6773
Advantage
87
Frontier Scientific, Inc.
Tel
--
Fax
--
Email
sales@frontiersci.com
Country
United States
ProdList
6222
Advantage
86
Matrix Scientific
Tel
--
Fax
--
Email
sales@matrixscientific.com
Country
United States
ProdList
6632
Advantage
80
3B Scientific Corporation
Tel
--
Fax
--
Email
sales@3bsc.com
Country
United States
ProdList
6962
Advantage
56
Reddy Chemtech Inc.
Tel
--
Fax
--
Email
sales@reddychemtech.com
Country
United States
ProdList
224
Advantage
0
Combi-Blocks Inc.
Tel
--
Fax
--
Email
sales@combi-blocks.com
Country
United States
ProdList
6618
Advantage
69
Waterstone Technology, LLC
Tel
--
Fax
--
Email
sales@waterstonetech.com
Country
United States
ProdList
6786
Advantage
30
Chem-Impex International, Inc.
Tel
--
Fax
--
Country
United States
ProdList
6730
Advantage
64
Ryan Scientific, Inc.
Tel
--
Fax
--
Email
ryan.reichlyn@ryansci.com
Country
United States
ProdList
6439
Advantage
60
Penta Manufacturing Company
Tel
--
Fax
--
Email
sales@pentamfg.com
Country
United States
ProdList
5076
Advantage
65
Alfa Aesar
Tel
--
Fax
--
Email
tech@alfa.com
Country
United States
ProdList
6814
Advantage
81
Beta Pharma, Inc.
Tel
--
Fax
--
Email
sales@betapharma.com
Country
United States
ProdList
6226
Advantage
60
HONEST JOY HOLDINGS LIMITED
Tel
--
Fax
--
Email
sales@honestjoy.cn
Country
United States
ProdList
6675
Advantage
54
2A PharmaChem USA
Tel
--
Fax
--
Email
sales@2apharmachem.com
Country
United States
ProdList
6137
Advantage
39
3B Scientific Corporation
Tel
--
Fax
--
Email
sales@3bsc.com
Country
United States
ProdList
6718
Advantage
47
Chemiplus Corporation
Tel
--
Fax
--
Email
okazaki@chemiplus.com
Country
United States
ProdList
3198
Advantage
38
Advance Scientific & Chemical
Tel
--
Fax
--
Email
sales@advance-scientific.com
Country
United States
ProdList
6419
Advantage
71
Spectrum Chemicals & Laboratory Products
Tel
--
Fax
--
Email
sales@spectrumchemical.com
Country
United States
ProdList
6699
Advantage
77
MP Biomedicals, Inc.
Tel
--
Fax
--
Country
United States
ProdList
6561
Advantage
81
City Chemicals Corporation
Tel
--
Fax
--
Country
United States
ProdList
6460
Advantage
72
Wilshire Chemical Company Inc.
Tel
--
Fax
--
Email
WilshrChem@AOL.COM
Country
United States
ProdList
3498
Advantage
58
More
Less

View Lastest Price from 6-Methylquinoline manufacturers

Hebei Chuanghai Biotechnology Co,.LTD
Product
6-Methylquinoline 91-62-3
Price
US $10.70/kg
Min. Order
10kg
Purity
99%
Supply Ability
10000kg
Release date
2024-08-20
Hebei Kingfiner Technology Development Co.Ltd
Product
6-Methylquinoline 91-62-3
Price
US $0.00-0.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
50000kg
Release date
2023-11-03
Shaanxi Dideu Medichem Co. Ltd
Product
6-Methylquinoline 91-62-3
Price
US $0.00-0.00/Kg
Min. Order
100G
Purity
99.0%+
Supply Ability
100 tons
Release date
2020-01-17

91-62-3, 6-MethylquinolineRelated Search:


  • 6-methyl-quinolin
  • p-Methylquinoline
  • FEMA 2744
  • 6-METHYLQUINOLINE
  • P-TOLUQUINOLINE
  • PARA METHYL QUINOLINE
  • 6-METHYLQUINOLINE 98+%
  • Quinoline, 6-methyl-
  • 8-Methyl-5-(trifluoromethyl)quinoline
  • 6-methyquinoline
  • 4-Quinoline-carboxamide
  • 4-Quinoline-carboxylic Hydrazide
  • 4-Thioquinoline-carboxamide
  • Ethyl 4-Quinoline-carboxylate
  • 3-Chloro-7-methylisoquinoline
  • 4-(Piperidin-1-yl)-8-(trifluoromethyl)quinoline
  • 7-bromo-6-chloroquinazolin-4(3H)-one
  • 6-Methylquinoline,95%
  • 6-Methylchinolin
  • M & S BASAL MEDIUM w/VITAMINS
  • 6-Methylquinoline&gt
  • 6-Methylquinoline USP/EP/BP
  • Phytotech-M&S BASAL MEDIUM w/VITAMINS MS
  • 6-Methylquinoline50
  • Glycerol Impurity 113
  • 6-Methylquinoline, ≥ 98.0%
  • 6-Methylquinoline in isooctane
  • 91-62-3
  • CH3C6H3NCHCHCH
  • Alkylquinolines
  • Quinolines
  • Heterocyclic Building Blocks
  • Building Blocks
  • Alkylquinolines
  • FluoroCompounds
  • blocks
  • Quinolines
  • Quinoline&Isoquinoline
  • Quinoline Derivertives