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Quinaldine

Quinaldine Structure
CAS No.
91-63-4
Chemical Name:
Quinaldine
Synonyms
2-METHYLQUINOLINE;2-Methylchinolin;QuinaL;2-Methylpuinoiline;2-METHYLQUINOLINES;NSC-3397;Quildine;Khinaldin;QUINALDINE;Chinaldine
CBNumber:
CB7373558
Molecular Formula:
C10H9N
Molecular Weight:
143.19
MOL File:
91-63-4.mol
MSDS File:
SDS
Modify Date:
2024/8/24 19:19:26

Quinaldine Properties

Melting point -2 °C
Boiling point 248 °C
Density 1.058 g/mL at 25 °C(lit.)
vapor pressure <0.1 hPa (20 °C)
refractive index n20/D 1.612(lit.)
Flash point 175 °F
storage temp. Store below +30°C.
solubility chloroform: soluble(lit.)
pka 5.83(at 20℃)
form Crystalline Powder
color White to slightly yellow
PH 6.9 (H2O, 20℃)(saturated aqueous solution)
Water Solubility PRACTICALLY INSOLUBLE
Sensitive Light Sensitive
Merck 14,8047
BRN 110309
Stability Stable, but may be light sensitive. Combustible. Incompatible with strong oxidizing agents.
LogP 2.59
CAS DataBase Reference 91-63-4(CAS DataBase Reference)
NIST Chemistry Reference Quinoline, 2-methyl-(91-63-4)
EPA Substance Registry System Quinaldine (91-63-4)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07,GHS08
Signal word  Warning
Hazard statements  H302+H312-H315-H319-H341-H412
Precautionary statements  P273-P280-P301+P312-P302+P352+P312-P305+P351+P338-P308+P313
Hazard Codes  Xn
Risk Statements  21/22-68-36/37/38
Safety Statements  36-45-36/37/39-26
RIDADR  NA 1993 / PGIII
WGK Germany  3
RTECS  UZ9625000
8-23
TSCA  Yes
HS Code  29334990
Toxicity LD50 orally in rats: 1.23 g/kg (Smyth)
NFPA 704
2
2 0

Quinaldine price More Price(14)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) Q2125 Quinaldine analytical standard, ≥90% (GC) 91-63-4 500ML ₹13607.03 2022-06-14 Buy
Sigma-Aldrich(India) Q2125 Quinaldine analytical standard, ≥90% (GC) 91-63-4 1L ₹27062.5 2022-06-14 Buy
Sigma-Aldrich(India) 8.05805 Quinaldine for synthesis 91-63-4 100ML ₹8450 2022-06-14 Buy
Sigma-Aldrich(India) 8.05805 Quinaldine for synthesis 91-63-4 250ML ₹11850 2022-06-14 Buy
Sigma-Aldrich(India) 22550 Quinaldine ≥95.0% (GC) 91-63-4 250ML ₹8530.1 2022-06-14 Buy
Product number Packaging Price Buy
Q2125 500ML ₹13607.03 Buy
Q2125 1L ₹27062.5 Buy
8.05805 100ML ₹8450 Buy
8.05805 250ML ₹11850 Buy
22550 250ML ₹8530.1 Buy

Quinaldine Chemical Properties,Uses,Production

Chemical Properties

Quinaldine or 2-methylquinoline is an organic compound with the formula CH3C9H6N. It is one of the methyl derivative of a heterocyclic compound quinoline. It is bioactive and is used in the preparation of various dyes. It is a colorless oil but commercial samples can appear colored.

Uses

Quinaldine is an anaesthetic used in fish transportation. Also used in anti-malaria drugs, in manufacturing dyes, food colorants , pharmaceuticals and pH indicators.

Definition

ChEBI: A quinoline compound in which the quinoline skeleton is substituted at C-2 with a methyl group.

Production Methods

High-temperature coal tar contains an average of 0.2% quinaldine. It is recovered from the quinoline base mixture by rectification and hydration. Quinaldine can be synthesized by the Skraup method from aniline and crotonaldehyde with sulfuric acid in the presence of a dehydrogenating agent.

General Description

A colorless oily liquid darkening to red-brown on exposure to air. Flash point 175°F. Denser than water and slightly soluble in water. Vapors heavier than air. Produces toxic oxides of nitrogen during combustion. Used to make dyes, pharmaceuticals and other chemicals.

Air & Water Reactions

Slightly soluble in water.

Reactivity Profile

Quinaldine 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. Keep tightly closed and protected from light .

Hazard

Strong irritant to mucous membranes.

Fire Hazard

Quinaldine is probably combustible.

Purification Methods

Dry it with Na2SO4 or by refluxing with BaO, then fractionally distil it under reduced pressure and redistil it from zinc dust. Purify it further by conversion to its phosphate (m 220o) or picrate (m 192o) from which after recrystallisation, the free base is regenerated. [Packer et al. J Am Chem Soc 80 905 1958.] Its ZnCl2 complex can be used for the same purpose. [Beilstein 20 III/IV 3454, 20 V 375.]

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