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Merck

F20009

Furfurylamine

≥99%

Sinónimos:

2-Aminomethylfuran

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5 G

US$ 48,80

100 G

US$ 51,20

US$ 48,80

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Fórmula empírica (notación de Hill):
C5H7NO
Número CAS:
617-89-0
Peso molecular:
97.12
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24894804
EC Number:
210-536-9
Beilstein/REAXYS Number:
1614
MDL number:
MFCD00003258

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Nombre del producto

Furfurylamine, ≥99%

InChI

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

InChI key

DDRPCXLAQZKBJP-UHFFFAOYSA-N

SMILES string

NCc1ccco1

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.)

Quality Level

100

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1 of 4

Este artículo
319910A77997A88182
Furfurylamine ≥99%

Sigma-Aldrich

F20009

Furfurylamine

Furfural ACS reagent, 99%

Sigma-Aldrich

319910

Furfural

2-Aminopyridine 99%

Sigma-Aldrich

A77997

2-Aminopyridine

o-Anisidine ≥99%

Sigma-Aldrich

A88182

o-Anisidine

assay

≥99%

assay

99%

assay

99%

assay

≥99%

Quality Level

100

Quality Level

200

Quality Level

100

Quality Level

200

form

liquid

form

liquid

form

crystals

form

liquid

refractive index

n20/D 1.490 (lit.)

refractive index

n20/D 1.525 (lit.)

refractive index

-

refractive index

n20/D 1.574 (lit.)

density

1.099 g/mL at 25 °C (lit.)

density

1.16 g/mL at 25 °C (lit.)

density

-

density

1.092 g/mL at 25 °C (lit.)

mp

−70 °C (lit.)

mp

−36 °C (lit.)

mp

54-58 °C (lit.)

mp

3-6 °C (lit.)

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).

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Danger

Hazard Classifications

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

Clase de almacenamiento

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

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

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Certificados de análisis (COA)

Lot/Batch Number
MKDB0225
MKCX4666
MKCV7972
MKCR4489
MKCP2937

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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
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
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:
Wei Gao et al.
Ultrasonics sonochemistry, 44, 152-161 (2018-04-24)
The present study has reported an optimized fabrication and application of a novel PVA/TEOS/Schiff base nanofibers membrane as a highly sensitive copper (II) ions in aqueous environment. Here in, for first time, an ultrasound-assisted synthesized symmetric Schiff base has been
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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