Furfurylamine

Structural formula
General
Surname	Furfurylamine
other names	2-furan methanamine α-furfurylamine Furan-2-methylamine 2-aminomethylfuran 2-furylmethylamine
Molecular formula	C 5 H 7 NO
Brief description	colorless liquid with an amine-like odor
External identifiers / databases
CAS number 617-89-0 EC number 210-536-9 ECHA InfoCard 100.009.580 PubChem 3438 Wikidata Q5509528
properties
Molar mass	97.12 g mol −1
Physical state	liquid
density	1.05 g cm −3
Melting point	-70 ° C
boiling point	146 ° C
Vapor pressure	4 hPa (20 ° C)
solubility	completely miscible with water
Refractive index	1.4886
safety instructions
GHS labeling of hazardous substances danger H and P phrases H: 226-302-312-332-314 P: 210-280-301 + 330 + 331-303 + 361 + 353-305 + 351 + 338-304 + 340-310
As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions . Refractive index: Na-D line , 20 ° C

Furfurylamine is a chemical compound from the group of amines and furans . It was described as early as the 19th century.

Extraction and presentation

Furfurylamine can be obtained from furfural and ammonia by catalytic reductive amination .

use

Furfurylamine is used as a synthesis base for dyes, synthetic resins, pharmaceuticals and rubber chemicals.

Individual evidence

1. ↑ ^{a b c d e f g} Entry on furfurylamine in the GESTIS substance database of the IFA , accessed on February 1, 2016(JavaScript required) .
2. ↑ Data sheet 2-Fufurylamine ( Memento of the original from January 9, 2015 in the Internet Archive ) Info: The archive link has been inserted automatically and has not yet been checked. Please check the original and archive link according to the instructions and then remove this notice. . 
3. ↑ ^{a b} Author collective: Organikum: organic-chemical basic internship . Wiley-VCH, Weinheim u. a. 2001, ISBN 3-527-29985-8 , p. 585.
4. ↑ GL Ciamician, M. Dennstedt: Ueber das Furfurylamin . In: Reports of the German Chemical Society . tape 14 , no. 1 , January 1881, p. 1475-1477 , doi : 10.1002 / cber.188101401309 .
5. ↑ Entry on furfurylamine. In: Römpp Online . Georg Thieme Verlag, accessed on January 9, 2015.