Q809
Quinaldine
≥95%
Synonym(s):
2-Methylquinoline
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About This Item
Empirical Formula (Hill Notation):
C10H9N
CAS Number:
Molecular Weight:
143.19
EC Number:
202-085-1
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
110309
MDL number:
Quality Level
assay
≥95%
refractive index
n20/D 1.612 (lit.)
bp
105-107 °C/10 mmHg (lit.), 248 °C (lit.)
mp
−9-−3 °C (lit.)
density
1.058 g/mL at 25 °C (lit.)
SMILES string
Cc1ccc2ccccc2n1
InChI
1S/C10H9N/c1-8-6-7-9-4-2-3-5-10(9)11-8/h2-7H,1H3
InChI key
SMUQFGGVLNAIOZ-UHFFFAOYSA-N
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signalword
Warning
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Irrit. 2 - Muta. 2 - Skin Irrit. 2
Storage Class
10 - Combustible liquids
wgk
WGK 3
flash_point_f
174.2 °F - closed cup
flash_point_c
79 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Regulatory Information
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Yongmei Li et al.
Journal of hazardous materials, 173(1-3), 151-158 (2009-09-08)
The anaerobic degradation of quinoline, isoquinoline and 2-methylquinoline was investigated under nitrate-reducing conditions with acclimated activated sludge. Quinoline was completely transformed during degradation with an optimum COD/NO(3)-N ratio of 7. Isoquinoline and 2-methylquinoline were also completely transformed; however, nitrate consumption
J Ortuño et al.
Fish & shellfish immunology, 12(1), 49-59 (2002-02-28)
Anaesthesia may depress the immune system in mammals, but there is no available information on this topic in fish. In the present work, four anaesthetics that are used in aquaculture, MS222 (0 19 mM), benzocaine (0.21 mM), 2-phenoxyethanol (16 mM)
M Naoi et al.
Life sciences, 40(11), 1075-1082 (1987-03-16)
Type A monoamine oxidase (MAO-A) in human placental mitochondria was competitively inhibited by naturally occurring substances, quinoline and quinaldine, using kynuramine as substrate. Quinoline had a higher affinity for MAO than kynuramine. MAO-A in human brain synaptosomal mitochondria was also