93627-55-5

Basic information

• Product Name: EMMPI
• Synonyms: EMMPI
• CAS NO: 93627-55-5
• Molecular Formula: C9H20INO
• Molecular Weight: 285.16567
• EINECS: -0
• Mol File: 93627-55-5.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: EMMPI(CAS DataBase Reference)
• NIST Chemistry Reference: EMMPI(93627-55-5)
• EPA Substance Registry System: EMMPI(93627-55-5)

Safety Data

• Hazardous Substances Data: 93627-55-5(Hazardous Substances Data)

Usage

Description

EMMPI, also known as ethyl-3-methyl-3-phenylglycidate, is a synthetic chemical compound that is widely used in the fragrance industry. It is characterized by its sweet, fruity, and berry-like aroma, making it a popular choice for flavoring agents in food and beverages. Additionally, EMMPI is utilized in the production of perfumes and personal care products due to its pleasant and long-lasting scent.
Usage:
Used in Food and Beverage Industry:
EMMPI is used as a flavoring agent for its sweet, fruity, and berry-like taste, enhancing the overall flavor profile of various food and beverage products.
Used in Perfume Industry:
EMMPI is used as a fragrance ingredient in perfumes, contributing to their pleasant and long-lasting aroma.
Used in Personal Care Products:
EMMPI is used in personal care products such as soaps, lotions, and creams, providing a sweet, fruity, and berry-like scent that is appealing to consumers.

Upstream product

• 109-02-4 4-methyl-morpholine 
• 542-69-8 1-iodo-butane 
• 93627-56-6 4-Isopropyl-4-methyl-morpholin-4-ium; iodide 

Relevant articles and documents

Conveniant Method for Replacement of Tertiary N-Methyl by Other Alkyl Groups: Application to Morphine Alkaloids

The replacement of N-methyl of N-methylpiperidine (1), 4-methylmorpholine (4), 2-methyl-1,2,3,4-tetrahydroisoquinoline (7) and tropine (10) by n-propyl, n-butyl and isopropyl groups (3a-3c, 6c, 9a-9c and 12a-12c) has been achieved in high yields by quaternization of the respective tertiary amine with appropriate alkyl halide and demethylation of the resulting quaternary salt with thiophenoxide.It has been established that demethylation is strongly favoured over the removal of n-propyl and n-butyl groups, whereas deisopropylation occurs to some extent.Surprisingly, in the case of 11c, deisopropylation predominates.This method has been applied to morphine (13b), codeine (13d) and thebaine (14b) for similar replacements.The rapid quaternization of thebaine (14b) has been assigned to the absence of H-14 in this alkaloid.The fact that quaternary salts of thebaine, which are susceptible to aromatization of the nucleus by extrusion of the ethanamine chain, are smoothly demethylated to N-alkylnorthebaines (18a-18c) in good yields indicates that demethylation, a bimolecular nucleophilic displacement, competes very successfully with elimination reaction.