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Merck

04623

Supelco

Furfural

analytical standard

동의어(들):

2-Furaldehyde, Furan-2-carboxaldehyde

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크기 선택

제품정보 (DICE 배송 시 비용 별도)

실험식(Hill 표기법):
C5H4O2
CAS 번호:
98-01-1
Molecular Weight:
96.08
Beilstein:
105755
EC Number:
202-627-7
MDL number:
MFCD00003229
UNSPSC 코드:
85151701
PubChem Substance ID:
329747960
NACRES:
NA.24

주요 문서

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도움 문의

Quality Level

100

Grade

analytical standard

vapor density

3.31 (vs air)

vapor pressure

13.5 mmHg ( 55 °C)

분석

≥98.5% (GC)

autoignition temp.

599 °F

유통기한

limited shelf life, expiry date on the label

expl. lim.

19.3 %

불순물

≤0.5% water

refractive index

n20/D 1.522-1.528
n20/D 1.525 (lit.)

bp

162 °C (lit.)

mp

−36 °C (lit.)

density

1.16 g/mL at 25 °C (lit.)

응용 분야

cleaning products
cosmetics
flavors and fragrances
food and beverages
personal care

형식

neat

SMILES string

[H]C(=O)c1ccco1

InChI

1S/C5H4O2/c6-4-5-2-1-3-7-5/h1-4H

InChI key

HYBBIBNJHNGZAN-UHFFFAOYSA-N

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관련 카테고리

일반 설명

Furfural is a furan derivative obtained from renewable biomass-derived carbohydrates.

애플리케이션

Furfural is a sustainable alternative for petroleum-based building blocks used in the production of fine chemicals, plastics, etc and also offers a promising, rich platform for lignocellulosic biofuels.

픽토그램

FlameSkull and crossbonesHealth hazard
GHS02,GHS06,GHS08

신호어

Danger

Hazard Classifications

Acute Tox. 2 Inhalation - Acute Tox. 3 Oral - Acute Tox. 4 Dermal - Aquatic Chronic 3 - Carc. 2 - Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3

표적 기관

Respiratory system

Storage Class Code

3 - Flammable liquids

WGK

WGK 2

Flash Point (°F)

136.4 °F - closed cup

Flash Point (°C)

58 °C - closed cup

가장 최신 버전 중 하나를 선택하세요:

시험 성적서(COA)

Lot/Batch Number
BCCH1052
BCCD3142
BCCB3773
BCBT3539

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특정 버전이 필요한 경우 로트 번호나 배치 번호로 특정 인증서를 찾을 수 있습니다.

COA 검색

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문서 라이브러리에서 최근에 구매한 제품에 대한 문서를 찾아보세요.

문서 라이브러리 방문

Sofia Tallarico et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 250, 119367-119367 (2021-01-06)
Chemocatalytic conversion of cellulose into lactic acid is a valuable alternative to simple sugar fermentation. Nevertheless, the procedures still need optimization to be translated to the industrial scale. Such translation would benefit by on-line monitoring of reaction parameters by fast
Production of 5-hydroxymethylfurfural and furfural by dehydration of biomass-derived mono-and poly-saccharides.
Chheda JN, et al.
Green Chemistry, 9(4), 342-350 (2007)
T B Adams et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 35(8), 739-751 (1997-08-01)
The Expert Panel of the Flavor and Extract Manufacturers' Association (FEMA) has assessed the safety of furfural for its continued use as a flavour ingredient. The safety assessment takes into account the current scientific information on exposure, metabolism, pharmacokinetics, toxicology
Jean-Paul Lange et al.
ChemSusChem, 5(1), 150-166 (2012-01-04)
Furfural offers a promising, rich platform for lignocellulosic biofuels. These include methylfuran and methyltetrahydrofuran, valerate esters, ethylfurfuryl and ethyltetrahydrofurfuryl ethers as well as various C(10)-C(15) coupling products. The various production routes are critically reviewed, and the needs for improvements are
Reetta Karinen et al.
ChemSusChem, 4(8), 1002-1016 (2011-07-06)
Furfurals are important intermediates in the chemical industry. They are typically produced by homogeneous catalysis in aqueous solutions. However, heterogeneously catalyzed processes would be beneficial in view of the principles of green chemistry: the elimination of homogeneous mineral acids makes
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