Merck
CN
All Photos(1)

Documents

Safety Information

04623

Supelco

Furfural

analytical standard

Sign Into View Organizational & Contract Pricing

Synonym(s):
2-Furaldehyde, Furan-2-carboxaldehyde
Empirical Formula (Hill Notation):
C5H4O2
CAS Number:
Molecular Weight:
96.08
Beilstein:
105755
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.24

Quality Level

grade

analytical standard

vapor density

3.31 (vs air)

vapor pressure

13.5 mmHg ( 55 °C)

Assay

≥98.5% (GC)

autoignition temp.

599 °F

shelf life

limited shelf life, expiry date on the label

expl. lim.

19.3 %

impurities

≤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.)

application(s)

cleaning products
cosmetics
flavors and fragrances
food and beverages
personal care

format

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

Looking for similar products? Visit Product Comparison Guide

General description

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

Application

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.

Signal Word

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

Target Organs

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

Regulatory Information

危险化学品

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’.

Already Own This Product?

Documents related to the products that you have purchased in the past have been gathered in the Document Library for your convenience.

Visit the Document Library

Difficulty Finding Your Product Or Lot/Batch Number?

Product numbers are combined with Pack Sizes/Quantity when displayed on the website (example: T1503-25G). Please make sure you enter ONLY the product number in the Product Number field (example: T1503).

Example:

T1503
Product Number
-
25G
Pack Size/Quantity

Additional examples:

705578-5MG-PW

PL860-CGA/SHF-1EA

MMYOMAG-74K-13

1000309185

enter as 1.000309185)

Having trouble? Feel free to contact Technical Service for assistance.

Lot and Batch Numbers can be found on a product's label following the words 'Lot' or 'Batch'.

Aldrich Products

  • For a lot number such as TO09019TO, enter it as 09019TO (without the first two letters 'TO').

  • For a lot number with a filling-code such as 05427ES-021, enter it as 05427ES (without the filling-code '-021').

  • For a lot number with a filling-code such as STBB0728K9, enter it as STBB0728 without the filling-code 'K9'.

Not Finding What You Are Looking For?

In some cases, a COA may not be available online. If your search was unable to find the COA you can request one.

Request COA

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

Protocols

Separation of 5-Hydroxymethyl-2-furaldehyde; Furfuryl alcohol; Furfural; 2-Furyl methyl ketone; 5-Methyl-2-furaldehyde

Separation of Acetone; Acetic acid; Propionic acid; Ethyl butyrate; Ethanol; Isoamyl acetate; Isobutyric acid; 3-Methyl-2-butanol; Methyl acetate; 1-Propanol; Acetal, ≥98%, FG; 2-Methyl-1-pentanol; Butyl acetate; Ethyl propionate; 3-Pentanol; 2-Pentanol, 98%; Ethyl isobutyrate; Isobutyl acetate; Acetaldehyde; Furfural; Butyric acid; Methanol; Ethyl acetate

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service