| Identification | More | [Name]
CINNAMYLIDENEACETOPHENONE | [CAS]
614-57-3 | [Synonyms]
1,5-DIPHENYL-PENTA-2,4-DIEN-1-ONE
A-CINNAMYLIDENEACETOPHENONE
CINNAMYLIDENEACETOPHENONE
1,5-diphenyl-4-pentadien-1-one
2,4-Pentadien-1-one, 1,5-diphenyl-
5-phenyl-2,4-pentadienophenone
5-phenyl-4-pentadienophenone
alpha-Cinnamylideneacetophenone
cinnamalacetophenone
5-phenylpenta-2,4-dienophenone
Cinnamylideneacetophenone, 98+%
1,5-diphenyl-2,4-pentadien-1-one
(4-Phenyl-1,3-butadienyl)phenyl ketone
Phenyl(4-phenyl-1,3-butadienyl) ketone | [EINECS(EC#)]
210-385-9 | [Molecular Formula]
C17H14O | [MDL Number]
MFCD00020692 | [Molecular Weight]
234.29 | [MOL File]
614-57-3.mol |
| Safety Data | Back Directory | [Symbol(GHS) ]
GHS07 | [Signal word ]
Warning | [Hazard statements ]
H315-H319-H335 | [Precautionary statements ]
P261-P280a-P304+P340-P305+P351+P338-P405-P501a | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection . | [RTECS ]
RZ2477000 |
| Hazard Information | Back Directory | [Description]
Colorless. viscous liquid. B.P. 239℃. Sp,Gr. 0.895. The aldehyde is conventionally sold in reduced strength, either 50% or 70% aldehyde content. The diluent may be the corresponding acetal, or an odorless solvent, e. g. Diethyl - phthalate. | [Uses]
Cinnamylideneacetophenone is used in perfume compositions as a floralizing aldehydic topnote ingredient, primariIy in Muguet-Lily fragrances, but also in Rose, Peony (where the Geranyl-isomer is claimed to lx superior), and various modifications of modern-aldehydic fragrance types. Occasionally used in flavor compositions for floral or fruity types, and in Rose type flavors. The concentration is usually mere traces in the finished product. | [Synthesis]
Cinnamylideneacetophenone is prepared from Citronellol, reacted with Sodium methylate or Sodium iso-propylate. The acetal is then prepared by reaction with Chlorodimethylacetal. The resulting acetal is finally hydrolyzed with diluted oxalic acid to yield the aldehyde. |
|
| Company Name: |
Alfa Aesar
|
| Tel: |
400-6106006 |
| Website: |
http://chemicals.thermofisher.cn |
| Company Name: |
Energy Chemical
|
| Tel: |
021-021-58432009 400-005-6266 |
| Website: |
http://www.energy-chemical.com |
| Company Name: |
Merck KGaA
|
| Tel: |
21-20338288 |
| Website: |
www.sigmaaldrich.cn |
|