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W270202

5-Methylfurfural

≥98%, FG

Synonym(e):

5-Methyl-furfural

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€ 48,00

100 G

€ 103,00

1 KG

€ 207,00

5 KG

€ 766,00

€ 48,00


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Über diesen Artikel

Empirische Formel (Hill-System):
C6H6O2
CAS-Nummer:
Molekulargewicht:
110.11
FEMA Number:
2702
Council of Europe no.:
119
UNSPSC Code:
12164502
PubChem Substance ID:
Flavis number:
13.001
EC Number:
210-622-6
NACRES:
NA.21
MDL number:
Beilstein/REAXYS Number:
106895
Organoleptic:
caramel; maple; spicy; sweet
Grade:
FG
Fragrance grade
Halal
Kosher
Biological source:
synthetic
Agency:
follows IFRA guidelines
meets purity specifications of JECFA
Food allergen:
no known allergens

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Produktname

5-Methylfurfural, ≥98%, FG

SMILES string

[H]C(=O)c1ccc(C)o1

InChI

1S/C6H6O2/c1-5-2-3-6(4-7)8-5/h2-4H,1H3

InChI key

OUDFNZMQXZILJD-UHFFFAOYSA-N

biological source

synthetic

grade

FG
Fragrance grade
Halal
Kosher

agency

follows IFRA guidelines
meets purity specifications of JECFA

reg. compliance

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

assay

≥98%

impurities

<0.1% DMF (residual starting material)

refractive index

n20/D 1.531 (lit.)

bp

187 °C (lit.)

density

1.107 g/mL at 25 °C (lit.)

application(s)

flavors and fragrances

documentation

see Safety & Documentation for available documents

food allergen

no known allergens

fragrance allergen

no known allergens

organoleptic

caramel; maple; spicy; sweet

storage temp.

2-8°C

Quality Level

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Dieser Artikel
W27021591307137316
grade

FG, Halal, Fragrance grade, Kosher

grade

FG, Fragrance grade, Halal, Kosher, natural

grade

analytical standard

grade

-

organoleptic

caramel; maple; spicy; sweet

organoleptic

bread; caramel; brown; spicy; sweet

organoleptic

-

organoleptic

-

biological source

synthetic

biological source

botanical

biological source

-

biological source

-

food allergen

no known allergens

food allergen

no known allergens

food allergen

-

food allergen

-

agency

follows IFRA guidelines, meets purity specifications of JECFA

agency

follows IFRA guidelines

agency

-

agency

-

documentation

see Safety & Documentation for available documents

documentation

see Safety & Documentation for available documents

documentation

-

documentation

-

Application


  • Metabolomics fingerprint of Philippine coffee by SPME-GC-MS for geographical and varietal classification.: This study employs solid-phase microextraction gas chromatography-mass spectrometry (SPME-GC-MS) to create a metabolomics fingerprint of Philippine coffee, identifying compounds like 5-Methylfurfural for the classification of coffee by geography and variety. This research highlights the potential of 5-Methylfurfural in distinguishing coffee varieties, showcasing its application in food biochemistry (Ongo et al., 2020).

General description

5-Methylfurfural has been identified as one of the volatile flavor compounds in tamarind[1], Dutch Coffee[2], barrel-aged wines[3] and deep fat-fried soybeans.[4]

Lagerklasse

10 - Combustible liquids

wgk

WGK 2

flash_point_f

161.6 °F - closed cup

flash_point_c

72 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


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Die Dokumentenbibliothek aufrufen

Volatile flavor components of deep fat-fried soybeans.
Wilkens WF & Lin FM.
Journal of Agricultural and Food Chemistry, 18, 337-339 (1970)
Studies on the Flavor Compounds of Dutch Coffee by Headspace GC-Mass.
Hwang SH, et al.
Korean journal of food and cookery science, 30(5), 596-602 (2014)
Formation and degradation of furfuryl alcohol, 5-methylfurfuryl alcohol, vanillyl alcohol, and their ethyl ethers in barrel-aged wines.
Spillman PJ, et al.
Journal of Agricultural and Food Chemistry, 46(2), 657-663 (1998)
Volatile flavor components of tamarind (Tamarindus indica L.).
Zhang Y, et al.
J. Essent. Oil Res., 2(4), 197-198 (1990)
Shahabuddin et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 29(10), 719-721 (1991-10-01)
The furans, furfural and methylfurfural, are dietary mutagens that are present in various food products and beverages. AT base-pair-depleted calf thymus DNA was prepared by the action of pea seed single-strand-specific nuclease on native DNA. Compared with furan-treated native DNA

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