Skip to Content
Merck
CN
All Photos(2)

Documents

Safety Information

F20009

Sigma-Aldrich

Furfurylamine

≥99%

Synonym(s):

2-Aminomethylfuran

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C5H7NO
CAS Number:
Molecular Weight:
97.12
Beilstein:
1614
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

vapor density

3.35 (vs air)

Quality Level

vapor pressure

4 mmHg ( 20 °C)

Assay

≥99%

form

liquid

refractive index

n20/D 1.490 (lit.)

bp

145-146 °C (lit.)

mp

−70 °C (lit.)

density

1.099 g/mL at 25 °C (lit.)

SMILES string

NCc1ccco1

InChI

1S/C5H7NO/c6-4-5-2-1-3-7-5/h1-3H,4,6H2

InChI key

DDRPCXLAQZKBJP-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Application

  • Synthesis of renewable furan-based flame retardants: Research describes the synthesis of renewable furan-based phosphate, utilizing furfurylamine, for superior flame retardancy in biodegradable polylactide, showcasing its potential in enhancing material safety (Li et al., 2024).
  • Flame retardant for biomass-based fabrics: The development of a molecularly engineered, fully bio-derived phosphorylated furan-based flame retardant, involving furfurylamine, for biomass-based fabrics highlights advancements in fire safety materials (Chen et al., 2024).
  • Near-infrared light-responsive composites: Furfurylamine is involved in the development of bio-benzoxazine/bio-urethane copolymers reinforced with graphene, which are NIR light-responsive shape memory composites, contributing to the field of smart materials (Jamnongpak et al., 2024).
  • Intelligent fire early-warning fabrics: A multifunctional polylactic acid sensing fabric, using biomass flame retardants including furfurylamine, is developed for intelligent fire early-warning, demonstrating an integration of safety and technology (Jin et al., 2024).

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 2 Dermal - Acute Tox. 3 Oral - Acute Tox. 4 Inhalation - Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1B

WGK

WGK 1

Flash Point(F)

114.8 °F

Flash Point(C)

46 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

危险化学品

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Eduardo D Gomes et al.
Biomaterials, 105, 38-51 (2016-08-10)
Spinal Cord Injury (SCI) is a highly incapacitating condition for which there is still no cure. Current clinical approaches are mainly based on palliative care, so there is a need to find possible treatments to SCI. Cellular transplantation is regarded
Víctor Flors et al.
Planta, 216(6), 929-938 (2003-04-11)
1,2,3,4-tetra-O-acetyl-6-ethyladipate-beta- D-glucopyranose (TOGE), a glycoside derivative of adipic acid monoethyl ester and 1,2,3,4-tetra-O-acetyl-beta- D-glucopyranose, was synthesized and the resistance-inducing activity shown by TOGE-1 (TOGE plus furfurylamine) and TOGE-2 (TOGE plus 1,3-diaminepropane) was assayed. TOGE-1 and TOGE-2 protected tomato plants against
Amine Garci et al.
Acta crystallographica. Section E, Structure reports online, 67(Pt 11), m1592-m1592 (2012-01-06)
The single-crystal X-ray structure analysis of [RuCl(2)(C(12)H(18))(C(5)H(7)NO)] reveals a distorted piano-stool geometry around the Ru(II) atom, with a hexa-methyl-benzene ligand, two chloride ligands and a furfuryl-amine ligand, the latter coordinating through the amine group. In the crystal, a dimeric structure
Esteban Araya-Hermosilla et al.
Polymers, 13(3) (2021-01-27)
Among smart materials, self-healing is one of the most studied properties. A self-healing polymer can repair the cracks that occurred in the structure of the material. Polyketones, which are high-performance thermoplastic polymers, are a suitable material for a self-healing mechanism:
Cécile Ouairy et al.
The Journal of organic chemistry, 75(12), 4311-4314 (2010-05-27)
N-Acylation of furfurylamines provided 1, which on double deprotonation with LDA led to the formation of N-acyl-5-aminopenta-2,4-dienals 2 via an isomerization involving opening of the furan ring. The scope and limitations of the procedure were examined by considering the influence

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service