CAS Number67-47-0
SynonymsHMF; EINECS 200-654-9; 5-(Hydroxymethyl)furan-2-carboxaldehyde; T5OJ BVH E1Q; 5-(Hydroxymethyl)-2-furancarboxaldehyde; 5-(Hydroxymethyl)furan-2-carbaldehyde; Aes-103; 5-(Hydroxymethyl)furfural; 5-Hydroxymethylfurfural; MFCD00003234
Molecular FormulaC6H6O3
Molecular Weight126.11
Purity99%
Density1.3±0.1 g/cm3
Boiling Point114-116 °C/1 mmHg (lit.)
Melting Point28-34 °C (lit.)
AppearanceBeige colored crystalline solid
EINECS200-654-9
Symbol
Signal WordWarning
| Chemical & Physical Properties | |
|---|---|
| CAS Number | 67-47-0 |
| Catalog No. | 2A-9006571 |
| Chinese Name | 5-羟甲基糠醛 |
| Synonyms | HMF; EINECS 200-654-9; 5-(Hydroxymethyl)furan-2-carboxaldehyde; T5OJ BVH E1Q; 5-(Hydroxymethyl)-2-furancarboxaldehyde; 5-(Hydroxymethyl)furan-2-carbaldehyde; Aes-103; 5-(Hydroxymethyl)furfural; 5-Hydroxymethylfurfural; MFCD00003234 |
| Molecular Formula | C6H6O3 |
| Molecular Weight | 126.11 |
| Purity | 99 |
| Density | 1.3±0.1 g/cm3 |
| Boiling Point | 114-116 °C/1 mmHg (lit.) |
| Melting Point | 28-34 °C (lit.) |
| Appearance | Beige colored crystalline solid |
| Water Solubility | Water solubility: completely dissolved; easily sol |
| Storage Condition | This product should be sealed with argon gas and s |
| Packaging | III |
| Application | 5-(Hydroxymethyl)furan-2-carbaldehyde, derived from woody biomass, inhibits yeast growth and fermentation. |
| EINECS | 200-654-9 |
| HTC | 2932190090 |
| PubChem ID | 24895618 |
| MDL Number | MFCD00003234 |
| SMILES | [H]C(=O)c1ccc(CO)o1 |
| InChI | 1S/C6H6O3/c7-3-5-1-2-6(4-8)9-5/h1-3,8H,4H2 |
| InChI Key | NOEGNKMFWQHSLB-UHFFFAOYSA-N |
| Beilstein/REAXYS | 110889 |
| NACRES Code | NA.22 |
| UNSPSC | 12352100 |
| Hazard Symbols | Transport |
| MSDS | msds/6571_1_67_47_0.pdf |
| Bioactivity | 5-(Hydroxymethyl)furan-2-carbaldehyde, derived from lignocellulosic biomass, inhibits yeast growth and fermentation as stressors. Related Catalog Signaling Pathways >> Anti-infection >> Fungal Natural Products >> Acids and Aldehydes Research Areas >> Others Target Yeast[1]. In Vitro It is found that furfural and HMF cause the attenuation of bulk translation activity and the assembly of cytoplasmic mRNP granules in Saccharomyces cerevisiae. Notably, a combination of furfural and HMF induce the remarkable repression of translation initiation and SG formation. Furfural and HMF can induce the formation of cytoplasmic mRNP granules, HMF also causes a gradual reduction in the polysome fraction and a concomitant increase in the 80S monosome fraction[1]. References [1]. Iwaki A, et al. Biomass conversion inhibitors furfural and 5-hydroxymethylfurfural induce formation of messenger RNP granules and attenuate translation activity in Saccharomyces cerevisiae. Appl Environ Microbiol. 2013 Mar;79(5):1661-7. Chemical & Physical Properties Density 1.3±0.1 g/cm3 Boiling Point 291.5±30.0 °C at 760 mmHg Melting Point 28-34 °C(lit.) Molecular Formula C6H6O3 Molecular Weight 126.110 Flash Point 79.4±0.0 °C Exact Mass 126.031693 PSA 50.44000 LogP -0.45 Vapour Pressure 0.0±0.6 mmHg at 25°C Index of Refraction 1.563 InChIKey NOEGNKMFWQHSLB-UHFFFAOYSA-N SMILES O=Cc1ccc(CO)o1 Storage condition 2-8°C Stability Light Sensitive, Very Hygroscopic |
| Use of | 5-(Hydroxymethyl)furan-2-carbaldehyde, derived from lignocellulosic biomass, inhibits yeast growth and fermentation as stressors. Properties Articles87 Name 5-hydroxymethylfurfural Synonym More Synonyms 5-hydroxymethylfurfural Biological Activity Description 5-(Hydroxymethyl)furan-2-carbaldehyde, derived from lignocellulosic biomass, inhibits yeast growth and fermentation as stressors. Related Catalog Signaling Pathways >> Anti-infection >> Fungal Natural Products >> Acids and Aldehydes Research Areas >> Others In Vitro It is found that furfural and HMF cause the attenuation of bulk translation activity and the assembly of cytoplasmic mRNP granules in Saccharomyces cerevisiae. Notably, a combination of furfural and HMF induce the remarkable repression of translation initiation and SG formation. Furfural and HMF can induce the formation of cytoplasmic mRNP granules, HMF also causes a gradual reduction in the polysome fraction and a concomitant increase in the 80S monosome fraction[1]. References [1]. Iwaki A, et al. Biomass conversion inhibitors furfural and 5-hydroxymethylfurfural induce formation of messenger RNP granules and attenuate translation activity in Saccharomyces cerevisiae. Appl Environ Microbiol. 2013 Mar;79(5):1661-7. Chemical & Physical Properties Molecular Formula C6H6O3 Exact Mass 126.031693 PSA 50.44000 LogP -0.45 Index of Refraction 1.563 InChIKey NOEGNKMFWQHSLB-UHFFFAOYSA-N Stability Light Sensitive, Very Hygroscopic |
| Tax Rebate | 9.0% |
| Supervision | None MFN tariff: 6.5% Ordinary tariff: 20.0% |
| Transport Info | Shipping Name: UN |
| MSDS Transport Info | Module 14. Shipping information 14.1 UN dangerous goods number European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.2 United Nations shipping name European Land Transport Dangerous Regulations: Non-dangerous goods IMDG Code: Non-dangerous goods International air transport dangerous goods regulations: non-dangerous goods 14.3 Transport hazard categories European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.4 Package group European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.5 Environmental hazards European Land Transport Danger Regulations: No International Maritime Danger Regulations International Air Transport Danger Regulations: No Marine pollutants (yes/no): No 14.6 Special reminder to users No data available |
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