F20009
Furfurylamine
≥99%
Sinonimo/i:
2-Aminomethylfuran
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About This Item
Formula empirica (notazione di Hill):
C5H7NO
Numero CAS:
Peso molecolare:
97.12
Beilstein:
1614
Numero CE:
Numero MDL:
Codice UNSPSC:
12352100
ID PubChem:
NACRES:
NA.22
Prodotti consigliati
Densità del vapore
3.35 (vs air)
Livello qualitativo
Tensione di vapore
4 mmHg ( 20 °C)
Saggio
≥99%
Forma fisica
liquid
Indice di rifrazione
n20/D 1.490 (lit.)
P. eboll.
145-146 °C (lit.)
Punto di fusione
−70 °C (lit.)
Densità
1.099 g/mL at 25 °C (lit.)
Stringa SMILE
NCc1ccco1
InChI
1S/C5H7NO/c6-4-5-2-1-3-7-5/h1-3H,4,6H2
DDRPCXLAQZKBJP-UHFFFAOYSA-N
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Applicazioni
- 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).
Avvertenze
Danger
Indicazioni di pericolo
Classi di pericolo
Acute Tox. 2 Dermal - Acute Tox. 3 Oral - Acute Tox. 4 Inhalation - Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1B
Codice della classe di stoccaggio
3 - Flammable liquids
Classe di pericolosità dell'acqua (WGK)
WGK 1
Punto d’infiammabilità (°F)
114.8 °F - DIN 51755 Part 1
Punto d’infiammabilità (°C)
46 °C - DIN 51755 Part 1
Dispositivi di protezione individuale
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
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Wei Gao et al.
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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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In this work, we prepared electrically conductive self-healing nanocomposites. The material consists of multi-walled carbon nanotubes (MWCNT) that are dispersed into thermally reversible crosslinked polyketones. The reversible nature is based on both covalent (Diels-Alder) and non-covalent (hydrogen bonding) interactions. The
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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
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