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Quinaldine

Name: Quinaldine
Brand: SIAL

analytical standard, ≥90% (GC)

Synonym(s):

2-Methylquinoline

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About This Item

Empirical Formula (Hill Notation):

C₁₀H₉N

CAS Number:

91-63-4

Molecular Weight:

143.19

UNSPSC Code:

41116107

NACRES:

NA.24

PubChem Substance ID:

329823861

EC Number:

202-085-1

Beilstein/REAXYS Number:

110309

MDL number:

MFCD00006756

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Properties

grade

analytical standard

Quality Level

100

assay

≥90% (GC)

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

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.)

application(s)

forensics and toxicology
pharmaceutical (small molecule)

format

neat

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

Gene Information

human ... CYP1A2(1544)

Description

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

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This Item	Q2626	22550	A79000
Supelco Q2125 Quinaldine	Supelco Q2626 Quinaldine phosphate salt	Sigma-Aldrich 22550 Quinaldine	Sigma-Aldrich A79000 4-Aminoquinaldine
grade analytical standard	grade analytical standard	grade -	grade -
format neat	format neat	format -	format -
density 1.058 g/mL at 25 °C (lit.)	density 1.06 g/mL (lit.)	density 1.058 g/mL at 25 °C (lit.)	density -
mp −9-−3 °C (lit.)	mp -	mp −9-−3 °C (lit.)	mp 162-166 °C (lit.)
refractive index n20/D 1.612 (lit.)	refractive index -	refractive index n20/D 1.612 (lit.)	refractive index -
bp 105-107 °C/10 mmHg (lit.), 248 °C (lit.)	bp -	bp 105-107 °C/10 mmHg (lit.), 248 °C (lit.)	bp 333 °C (lit.)

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pictograms

GHS08,GHS07

signalword

Warning

hcodes

H302 + H312,H315,H319,H341,H412

pcodes

P273 - P280 - P301 + P312 - P302 + P352 + P312 - P305 + P351 + P338 - P308 + P313

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

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An in situ attenuated total reflection infrared study of a chiral catalytic solid-liquid interface: cinchonidine adsorption on pt.

D Ferri et al.

Journal of the American Chemical Society, 123(48), 12074-12084 (2001-11-29)

An in situ attenuated total reflection study of the chiral solid-liquid interface created by cinchonidine adsorption on a Pt/Al(2)O(3) model catalyst is presented. Experiments were performed in the presence of dissolved hydrogen, that is under conditions used for the heterogeneous

Effects of four anaesthetics on the innate immune response of gilthead seabream (Sparus aurata L.).

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)

Nitrate-dependent biodegradation of quinoline, isoquinoline, and 2-methylquinoline by acclimated activated sludge.

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

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Global Trade Item Number

SKU	GTIN
Q2125-500ML	04061838190444
Q2125-1L	04061838190437

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