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| | 2,4,5-Trimethylaniline Basic information |
| | 2,4,5-Trimethylaniline Chemical Properties |
| Hazard Codes | C | | WGK Germany | 2 | | RTECS | RG5925300 | | TSCA | TSCA listed | | 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). |
| | 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). | | Uses | 2,4,5-TRIMETHYLANILINE is used as fragrance. Primarily used in the formulation of fruit-based fragrances such as apple, and also as a fixative and harmonizing agent in rose-type fragrances. | | 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. |
| | 2,4,5-Trimethylaniline Preparation Products And Raw materials |
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