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4-METHOXY-3-HYDROXYACETOPHENONE 6100-74-9 4-METHOXY-3-HYDROXYACETOPHENONE 6100-74-9 4-METHOXY-3-HYDROXYACETOPHENONE 6100-74-9
Product Name: 4-METHOXY-3-HYDROXYACETOPHENONE
Synonyms: 3'-Hydroxy-4'-methoxyacetophenone 97%;-Hydroxy-4′;Diosmin EP Impurity A;Diosmin Impurity 1 (Diosmin EP Impurity A);3-HYDROXY-4-METHOXYACETOPHENONE;4'-METHOXY-3'-HYDROXYACETOPHENONE;4-METHOXY-3-HYDROXYACETOPHENONE;1-(3-hydroxy-4-methoxy-phenyl)ethanone
CAS: 6100-74-9
MF: C9H10O3
MW: 166.17
EINECS:
Product Categories: Aromatic Acetophenones & Derivatives (substituted)
Mol File: 6100-74-9.mol
4-METHOXY-3-HYDROXYACETOPHENONE Chemical Properties
Melting point 88-92 °C
Boiling point 329.9±27.0 °C(Predicted)
density 1.158
pka 9.15±0.10(Predicted)
Stability: Stable. Incompatible with strong oxidizing agents.
Safety Information
Hazard Codes Xn
Risk Statements 22
WGK Germany 3
MSDS Information
4-METHOXY-3-HYDROXYACETOPHENONE Usage And Synthesis
Chemical Properties solid
Uses Isoacetovanillone is a volatile compound isolated from oak wood. Also a byproduct in the production of Acetovanillone.
Preparation Preparation by saponification of 3-acetoxy-4-methoxy-acetophenone (90%) (59%).
Product Name: 4-METHOXY-3-HYDROXYACETOPHENONE
Synonyms: 3'-Hydroxy-4'-methoxyacetophenone 97%;-Hydroxy-4′;Diosmin EP Impurity A;Diosmin Impurity 1 (Diosmin EP Impurity A);3-HYDROXY-4-METHOXYACETOPHENONE;4'-METHOXY-3'-HYDROXYACETOPHENONE;4-METHOXY-3-HYDROXYACETOPHENONE;1-(3-hydroxy-4-methoxy-phenyl)ethanone
CAS: 6100-74-9
MF: C9H10O3
MW: 166.17
EINECS:
Product Categories: Aromatic Acetophenones & Derivatives (substituted)
Mol File: 6100-74-9.mol
4-METHOXY-3-HYDROXYACETOPHENONE Chemical Properties
Melting point 88-92 °C
Boiling point 329.9±27.0 °C(Predicted)
density 1.158
pka 9.15±0.10(Predicted)
Stability: Stable. Incompatible with strong oxidizing agents.
Safety Information
Hazard Codes Xn
Risk Statements 22
WGK Germany 3
MSDS Information
4-METHOXY-3-HYDROXYACETOPHENONE Usage And Synthesis
Chemical Properties solid
Uses Isoacetovanillone is a volatile compound isolated from oak wood. Also a byproduct in the production of Acetovanillone.
Preparation Preparation by saponification of 3-acetoxy-4-methoxy-acetophenone (90%) (59%).
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