Quinaldine

Modify Date: 2024-01-02 18:51:29

Quinaldine Structure
Quinaldine structure
 Common Name Quinaldine
CAS Number 91-63-4 Molecular Weight 143.185
Density 1.1±0.1 g/cm3 Boiling Point 246.5±0.0 °C at 760 mmHg
Molecular Formula C10H9N Melting Point -2 °C
MSDS Chinese USA Flash Point 79.4±0.0 °C
Symbol GHS07
GHS07		 Signal Word Warning

 Names

Name 2-Methylquinoline
Synonym More Synonyms

 Chemical & Physical Properties

Density 1.1±0.1 g/cm3
Boiling Point 246.5±0.0 °C at 760 mmHg
Melting Point -2 °C
Molecular Formula C10H9N
Molecular Weight 143.185
Flash Point 79.4±0.0 °C
Exact Mass 143.073502
PSA 12.89000
LogP 2.54
Vapour Pressure 0.0±0.4 mmHg at 25°C
Index of Refraction 1.625
Stability Stable, but may be light sensitive. Combustible. Incompatible with strong oxidizing agents.
Water Solubility PRACTICALLY INSOLUBLE

 Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :
UZ9625000
CHEMICAL NAME :
Quinaldine
CAS REGISTRY NUMBER :
91-63-4
BEILSTEIN REFERENCE NO. :
0110309
LAST UPDATED :
199806
DATA ITEMS CITED :
9
MOLECULAR FORMULA :
C10-H9-N
MOLECULAR WEIGHT :
143.20
WISWESSER LINE NOTATION :
T66 BNJ C1

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
Standard Draize test
ROUTE OF EXPOSURE :
Administration onto the skin
SPECIES OBSERVED :
Rodent - rabbit
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
1230 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Administration onto the skin
SPECIES OBSERVED :
Rodent - rabbit
DOSE/DURATION :
1870 uL/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value

MUTATION DATA

TYPE OF TEST :
Mutation in microorganisms
TEST SYSTEM :
Bacteria - Salmonella typhimurium
DOSE/DURATION :
2 umol/plate
REFERENCE :
CPBTAL Chemical and Pharmaceutical Bulletin. (Japan Pub. Trading Co., USA, 1255 Howard St., San Francisco, CA 94103) V.6- 1958- Volume(issue)/page/year: 36,4630,1988 *** NIOSH STANDARDS DEVELOPMENT AND SURVEILLANCE DATA *** NIOSH OCCUPATIONAL EXPOSURE SURVEY DATA : NOHS - National Occupational Hazard Survey (1974) NOHS Hazard Code - T0823 No. of Facilities: 33 (estimated) No. of Industries: 1 No. of Occupations: 4 No. of Employees: 28314 (estimated) NOES - National Occupational Exposure Survey (1983) NOES Hazard Code - T0823 No. of Facilities: 514 (estimated) No. of Industries: 9 No. of Occupations: 12 No. of Employees: 4782 (estimated) No. of Female Employees: 1548 (estimated)

 Safety Information

Symbol GHS07
GHS07
Signal Word Warning
Hazard Statements H302 + H312
Precautionary Statements P280
Personal Protective Equipment Eyeshields;Faceshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter
Hazard Codes Xn:Harmful
Risk Phrases R21/22;R36/37/38;R68
Safety Phrases S36-S45-S36/37/39-S26
RIDADR 2810.0
WGK Germany 3
RTECS UZ9625000
Hazard Class 6.1
HS Code 29334990

 Synthetic Route

 Customs

HS Code 2933499090
Summary 2933499090. other compounds containing in the structure a quinoline or isoquinoline ring-system (whether or not hydrogenated), not further fused. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

 Articles29

More Articles
The PaaX-type repressor MeqR2 of Arthrobacter sp. strain Rue61a, involved in the regulation of quinaldine catabolism, binds to its own promoter and to catabolic promoters and specifically responds to anthraniloyl coenzyme A.

J. Bacteriol. 195(5) , 1068-80, (2013)

The genes coding for quinaldine catabolism in Arthrobacter sp. strain Rue61a are clustered on the linear plasmid pAL1 in two upper pathway operons (meqABC and meqDEF) coding for quinaldine conversion ...

Quantitative structure-activity relationship analysis of inhibitors of the nicotine metabolizing CYP2A6 enzyme.

J. Med. Chem. 48 , 440-9, (2005)

The purpose of this study was to develop screening and in silico modeling methods to obtain accurate information on the active center of CYP2A6, a nicotine oxidizing enzyme. The inhibitory potencies o...

Exploring QSAR and QAAR for inhibitors of cytochrome P450 2A6 and 2A5 enzymes using GFA and G/PLS techniques

Eur. J. Med. Chem. 44 , 1941-51, (2009)

A series of naphthalene and non-naphthalene derivatives ( n = 42) having cytochrome P450 2A6 and 2A5 inhibitory activities, reported by Rahnasto et al., were subjected to QSAR and QAAR studies. The an...

 Synonyms

Quinoline, 2-methyl-
Quinaldine
MFCD00006756
EINECS 202-085-1
2-Methylquinoline
Fasudil Impurity 10
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