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Q2125

Supelco

Quinaldine

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
Beilstein:
110309
EC Number:
202-085-1
MDL number:
MFCD00006756
UNSPSC Code:
41116107
PubChem Substance ID:
329823861
NACRES:
NA.24

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)

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Application

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

Pictograms

Health hazardExclamation mark
GHS08,GHS07

Signal Word

Warning

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Irrit. 2 - Muta. 2 - Skin Irrit. 2

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

174.2 °F - closed cup

Flash Point(C)

79 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

FSL

Group 4: Flammable liquids
Type 3 petroleums
Hazardous rank III
Water insoluble liquid

JAN Code

Q2125-1L:
Q2125-VAR:
Q2125-BULK:
Q2125-100ML:
Q2125-500ML:

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Certificates of Analysis (COA)

Lot/Batch Number
MKCR0717
MKCN2375
MKCC0876
MKCK4174
MKCJ5033

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J L Allen et al.
Veterinary and human toxicology, 28 Suppl 1, 21-24 (1986-01-01)
Residue concentrations of drugs that are administered to fish by bath immersion are related primarily to passage of the drugs across the gills. The elimination of these chemicals by fish can be mediated by biotransformation, but the route of elimination
Heiko Niewerth et al.
BMC genomics, 13, 534-534 (2012-10-09)
Bacteria of the genus Arthrobacter are ubiquitous in soil environments and can be considered as true survivalists. Arthrobacter sp. strain Rue61a is an isolate from sewage sludge able to utilize quinaldine (2-methylquinoline) as sole carbon and energy source. The genome
Daniela Pucci et al.
Chemical communications (Cambridge, England), (19)(19), 2254-2256 (2008-05-09)
The synthesis of the first gallium(III)-based liquid crystal has been achieved grafting around the metal centre two chelating 2-methylquinolin-8-olate anions and one monodentate 3,4,5-tris(hexadecyloxy)benzoyloxy ligand, allowing the resulting complex to be a soft luminescent material with the typical high quantum
H Cope et al.
European journal of medicinal chemistry, 41(10), 1124-1143 (2006-06-20)
Transmissible spongiform encephalopathies (TSEs) are thought to arise from aggregation of a protease resistant protein denoted PrP(Sc), which is a misfolded isoform of the normal cellular prion protein PrP(C). Using virtual high-throughput screening we have selected structures analogous to acridine
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
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