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F20009

Sigma-Aldrich

Furfurylamine

≥99%

Synonym(s):

2-Aminomethylfuran

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About This Item

Empirical Formula (Hill Notation):
C5H7NO
CAS Number:
617-89-0
Molecular Weight:
97.12
Beilstein:
1614
EC Number:
210-536-9
MDL number:
MFCD00003258
UNSPSC Code:
12352100
PubChem Substance ID:
24894804
NACRES:
NA.22

vapor density

3.35 (vs air)

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

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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

H226,H301,H310,H314,H332

Hazard Classifications

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

Storage Class Code

3 - Flammable liquids

WGK

WGK 1

Flash Point(F)

114.8 °F - DIN 51755 Part 1

Flash Point(C)

46 °C - DIN 51755 Part 1

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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’.

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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
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:
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
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
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