N-Ethylaniline manufacturers and suppliers

N-Ethylaniline suppliers

Properties

Melting point:: -63 °C

Boiling point:: 205 °C(lit.)

Density: 0.963 g/mL at 25 °C(lit.)

vapor density: 4.2 (vs air)

vapor pressure: 0.2 mm Hg ( 25 °C)

refractive index: n20/D 1.554(lit.)

Flash point:: 185 °F

storage temp.: Store below +30°C.

solubility: 2.7g/l

form: Liquid

pka: 5.12(at 24℃)

color: Clear light yellow to light brown

PH: 11 (2.7g/l, H2O, 20℃)

explosive limit: 1.8-10.0%(V)

Water Solubility: 50 g/L (20 ºC)

Sensitive: Air & Light Sensitive

Merck: 14,3764

BRN: 507468

Exposure limits: NIOSH: IDLH 100 ppm

Dielectric constant: 5.9（20℃）

Stability:: Stable, but decomposes upon prolonged exposure to air or light. Combustible. Incompatible with strong oxidizing agents. May react violently with nitric acid.

LogP: 2.26 at 25℃ and pH6-8

Safety Information

Symbol(GHS): GHS06,GHS08

Signal word: Danger

Hazard statements: H301+H311+H331-H373

Precautionary statements: P260-P280-P301+P310-P302+P352+P312-P304+P340+P311-P314

Hazard Codes: T

Risk Statements: 23/24/25-33

Safety Statements: 28-37-45-28A

RIDADR: UN 2272 6.1/PG 3

WGK Germany: 1

RTECS: BX9780000

F: 8

Hazard Note: Toxic

TSCA: Yes

HazardClass: 6.1

PackingGroup: III

HS Code: 29214200

Toxicity: LD50 in rats (g/kg): 0.18 i.p., 0.28 orally, 4.7 s.c. (Sziza, Podhragyai)

Use

The metabolism of N-ethylaniline has been studied more as a tool to understanding microsomal drug metabolizing activity than as the central item of inquiry. However, the following have been clearly defined as metabolic products of N-ethylaniline: phenylhydroxylamine, N-hydroxyl, N-ethylaniline; N-ethyl-p-aminophenol; and aniline (Appel et al 1965; Heinze 1970; Hlavica 1970; Hlavica and Kiese 1969; Kampffmeyer and Kiese 1965; Kroeber et al 1970; Lange 1967 and Lange 1968). Nonmicrosomal metabolism has not been reported. Species shown capable of metabolism include rabbit, mouse, rat, dog, pig, and guinea pig with the proportions of the various metabolites often species dependent. Compounds similar to N-ethylaniline such as N-methyl-N-ethylaniline can form N-ethylaniline via demethylation (Gorrod et al 1975a,b).

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