Identification | Back Directory | [Name]
CORTEX ALDEHYDE 50 BENZYL ALCOHOL | [CAS]
2120-70-9 | [Synonyms]
CORTEX ALDEHYDE 2-(phenoxy)ethanal phenoxy-acetaldehyd PHENOXY ACETALDEHYDE CORTEX ALDEHYDE 50 P. 2-Phenoxyacetaldehyde Acetaldehyde, 2-phenoxy- ASINEX-REAG BAS 02858203 CORTEX ALDEHYDE 50 BENZYL ALCOHOL phenoxyacetaldehyde 50% in peomosa PHENOXY ACETALDEHYDE 50% IN BENZYL ALCOHOL CORTEX ALDEHYDE 50 BENZYL ALCOHOL USP/EP/BP | [EINECS(EC#)]
218-329-5 | [Molecular Formula]
C8H8O2 | [MDL Number]
MFCD00134414 | [MOL File]
2120-70-9.mol | [Molecular Weight]
136.15 |
Chemical Properties | Back Directory | [Melting point ]
38°C | [Boiling point ]
210.42°C (rough estimate) | [density ]
1.1150 (rough estimate) | [refractive index ]
1.5090 (estimate) | [storage temp. ]
Inert atmosphere,Store in freezer, under -20°C | [solubility ]
Ractically insoluble in water, soluble in alcohol and oils. | [form ]
viscous liquid | [color ]
Crystals | [Odor]
at 10.00 % in dipropylene glycol. fresh green cortex leafy hyacinth ozone leather | [Odor Type]
green | [LogP]
1.134 (est) | [EPA Substance Registry System]
Acetaldehyde, phenoxy- (2120-70-9) |
Hazard Information | Back Directory | [Occurrence]
Has apparently not been reported to occur in nature. | [Uses]
2-phenoxyacetaldehyde is used in perfume compositions. It performs particularly well with
the Ionones and Methylionones for woodyfloral complexes, and in Geranium for powerful, fresh-green effects. It can also give lift
and novel effects in Lavender with Oakmoss,
in Chypre, etc. It is an aldehyde of considerable versatility and power. | [Preparation]
From phenol in weak aqueous alkali with monochloroacetaldehyde dimethyl acetal to yield the acetal which is then hydrolysed. | [Safety Profile]
A skin irritant. When heated to decomposition it emits acrid smoke and irritating fumes. |
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