2,4,5-TRIMETHYLANILINE
2,4,5-TRIMETHYLANILINE Basic information
- Product Name:
- 2,4,5-TRIMETHYLANILINE
- Synonyms:
-
- 1-AMINO-2,4,5-TRIMETHYLBENZENE
- 2,4,5-TRIMETHYLAMINOBENZENE
- GERANYL BENZOATE
- FEMA 2511
- trans-3,7-dimethyl-2,6-octadien-1-ylbenzoate
- PSEUDOCUMIDINE
- PSI-CUMIDINE
- TIMTEC-BB SBB008592
- CAS:
- 94-48-4
- MF:
- C17H22O2
- MW:
- 258.36
- EINECS:
- 202-337-0
- Product Categories:
-
- Alphabetical Listings
- Flavors and Fragrances
- Amines and Anilines
- G-H
- Mol File:
- 94-48-4.mol
2,4,5-TRIMETHYLANILINE Chemical Properties
- Boiling point:
- 305 °C(lit.)
- Density
- 0.996 g/mL at 25 °C(lit.)
- FEMA
- 2511 | GERANYL BENZOATE
- refractive index
- n20/D 1.517(lit.)
- Flash point:
- >230 °F
- Odor
- at 100.00 %. sweet amber ylang rose
- Odor Type
- balsamic
- JECFA Number
- 860
- LogP
- 6.13
- CAS DataBase Reference
- 94-48-4(CAS DataBase Reference)
- EPA Substance Registry System
- 2,6-Octadien-1-ol, 3,7-dimethyl-, benzoate, (2E)- (94-48-4)
Safety Information
- Hazard Codes
- C
- WGK Germany
- 2
- RTECS
- RG5925300
- HazardClass
- AIR SENSITIVE, CORROSIVE
- Toxicity
- Both the acute oral LD50 value in rats and the acute dermal LD50 value in rabbits exceeded 5 g/kg (Moreno, 1973).
MSDS
- Language:English Provider:SigmaAldrich
2,4,5-TRIMETHYLANILINE Usage And Synthesis
Description
Geranyl benzoate has a sweet, light odor reminiscent of ylangylang. It may be synthesized from geraniol and benzoyl chloride in anhydrous pyridine; also from geraniol and benzoyl chloride using the Schotten-Bauman reaction.
Chemical Properties
Geranyl benzoate has a sweet, light odor reminiscent of ylang-ylang.
Occurrence
Has been reported in ylang ylang oil (Gildemeister & Hoffman, 1960).
Definition
ChEBI: Geranyl benzoate is a benzoate ester resulting from the formal condensation of the carboxy group of benzoic acid with the hydroxy group of geraniol. It has a role as a plant metabolite and a fragrance. It is a benzoate ester, a monoterpenoid and an olefinic compound. It is functionally related to a geraniol and a benzoic acid.
Preparation
From geraniol and benzoyl chloride in anhydrous pyridine; also from geraniol and benzoyl chloride using the Schotten– Baumman reaction.
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