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Merck

F20009

Sigma-Aldrich

Furfurylamin

≥99%

Synonym(e):

2-Aminomethyl-furan

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About This Item

Empirische Formel (Hill-System):
C5H7NO
CAS-Nummer:
Molekulargewicht:
97.12
Beilstein:
1614
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352100
PubChem Substanz-ID:
NACRES:
NA.22

Dampfdichte

3.35 (vs air)

Dampfdruck

4 mmHg ( 20 °C)

Assay

≥99%

Form

liquid

Brechungsindex

n20/D 1.490 (lit.)

bp

145-146 °C (lit.)

mp (Schmelzpunkt)

−70 °C (lit.)

Dichte

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

InChIKey

DDRPCXLAQZKBJP-UHFFFAOYSA-N

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Anwendung

  • 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).

Signalwort

Danger

Gefahreneinstufungen

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

Lagerklassenschlüssel

3 - Flammable liquids

WGK

WGK 1

Flammpunkt (°F)

114.8 °F - DIN 51755 Part 1

Flammpunkt (°C)

46 °C - DIN 51755 Part 1

Persönliche Schutzausrüstung

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


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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
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
Guilherme R Macedo Lima et al.
Polymers, 11(11) (2019-11-20)
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
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

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