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Merck

W248924

Sigma-Aldrich

糠醛

greener alternative

natural, ≥98%, FCC, FG

别名:

2-呋喃醛, 呋喃-2-甲醛

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About This Item

经验公式(希尔记法):
C5H4O2
CAS号:
分子量:
96.08
FEMA號碼:
2489
Beilstein:
105755
EC號碼:
MDL號碼:
分類程式碼代碼:
12164502
PubChem物質ID:
Flavis號碼:
13.018
NACRES:
NA.21

等級

FG
Fragrance grade
Halal
Kosher
natural

品質等級

agency

follows IFRA guidelines
meets purity specifications of JECFA

法律遵循

EU Regulation 1223/2009
EU Regulation 1334/2008 & 178/2002
FCC
FDA 21 CFR 117
FDA 21 CFR 175.105

蒸汽密度

3.31 (vs air)

蒸汽壓力

13.5 mmHg ( 55 °C)

化驗

≥98%

形狀

liquid

自燃溫度

599 °F

expl. lim.

19.3 %

環保替代產品特色

Less Hazardous Chemical Syntheses
Use of Renewable Feedstocks
Learn more about the Principles of Green Chemistry.

sustainability

Greener Alternative Product

折射率

n20/D 1.525 (lit.)

bp

162 °C (lit.)

mp

−36 °C (lit.)

溶解度

95% ethanol: soluble 1 mL/mL, clear

密度

1.16 g/mL at 25 °C (lit.)

應用

flavors and fragrances

文件

see Safety & Documentation for available documents

食物過敏原

no known allergens

香料過敏原

no known allergens

環保替代類別

感官的

almond; baked; bread; woody; sweet

SMILES 字串

[H]C(=O)c1ccco1

InChI

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

InChI 密鑰

HYBBIBNJHNGZAN-UHFFFAOYSA-N

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一般說明

Furfural is a furan derivative. Production of furfural by dehydration of fructose, glucose and xylose using a biphasic reactor system has been reported. Furfural, a Maillard reaction product, is reported to inhibit the growth and alcohol production bySaccharomyces cerevisiae.
We are committed to bringing you Greener Alternative Products, which adhere to one of the four categories of Greener Alternatives . This product is a Biobased products, showing key improvements in Green Chemistry Principles “Less Hazardous Chemical Syntheses” and “Use of Renewable Feedstock”.

訊號詞

Danger

危險分類

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

標靶器官

Respiratory system

儲存類別代碼

3 - Flammable liquids

水污染物質分類(WGK)

WGK 2

閃點(°F)

136.4 °F - closed cup

閃點(°C)

58 °C - closed cup

個人防護裝備

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


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分析证书(COA)

Lot/Batch Number

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访问文档库

Inhibition of glycolysis by furfural in Saccharomyces cerevisiae.
Banerjee N, et al.
Europ. J. Appl. Microbiol. Biotechnol., 11(4), 226-228 (1981)
Selective conversion of furfural to methylfuran over silica-supported Ni Fe bimetallic catalysts.
Sitthisa S, et al.
J. Catal., 284(1), 90-101 (2011)
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)
Selective hydrogenation of furfural and levulinic acid to biofuels on the ecofriendly Cu-Fe catalyst.
Yan K and Chen A.
Fuel: The Science and Technology of Fuel and Energy, 115, 101-108 (2014)
Jianmin Zhang et al.
Journal of medicinal chemistry, 50(8), 1850-1864 (2007-03-27)
The 3C-like protease (3CLpro), which controls the severe acute respiratory syndrome (SARS) coronavirus replication, has been identified as a potential target for drug design in the treatment of SARS. A series of tetrapeptide phthalhydrazide ketones, pyridinyl esters, and their analogs

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