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Isopropyl cyclopropane carboxylate, with the chemical formula C8H14O2, is a carboxylic ester known for its fruity, apple-like odor. It is recognized for its safe use in various applications, including as a flavoring agent in the food and beverage industry, a component in fragrance formulations, and a solvent across different industrial sectors.

6887-83-8

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6887-83-8 Usage

Uses

Used in Food and Beverage Industry:
Isopropyl cyclopropane carboxylate is used as a flavoring agent to impart a distinctive apple-like flavor to various food and beverage products, enhancing their taste profiles without posing any known health risks.
Used in Fragrance Industry:
ISOPROPYL CYCLOPROPANE CARBOXYLATE serves as an important ingredient in fragrance formulations, where its fruity aroma contributes to the creation of appealing scents for perfumes and other scented products.
Used in Cosmetic Products:
Isopropyl cyclopropane carboxylate is utilized in cosmetic products for its pleasant odor, adding to the sensory experience of these products while maintaining safety standards.
Used as a Solvent in Various Industries:
Its solvent properties make isopropyl cyclopropane carboxylate a valuable component in a range of industrial applications, facilitating processes that require the dissolution of other substances.

Check Digit Verification of cas no

The CAS Registry Mumber 6887-83-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,8,8 and 7 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6887-83:
(6*6)+(5*8)+(4*8)+(3*7)+(2*8)+(1*3)=148
148 % 10 = 8
So 6887-83-8 is a valid CAS Registry Number.
InChI:InChI=1/C7H12O2/c1-5(2)9-7(8)6-3-4-6/h5-6H,3-4H2,1-2H3

6887-83-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name propan-2-yl cyclopropanecarboxylate

1.2 Other means of identification

Product number -
Other names Isopropyl cyclopropane carboxyliate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:6887-83-8 SDS

6887-83-8Downstream Products

6887-83-8Relevant academic research and scientific papers

Ester cyclopropanecarboxylate solvent-free synthesis method

-

Paragraph 0045; 0046, (2016/12/16)

The invention discloses an ester cyclopropanecarboxylate solvent-free synthesis method. According to the synthesis method, 4-halogenated butyric ester is used as raw materials; under the effects of ion liquid and inorganic strong alkali, a target product of the ester cyclopropanecarboxylate is obtained. The synthesis method provided by the invention has the advantages that the use of a solvent is not needed; only the ion liquid and the inorganic alkali need to be added; the ester cyclopropanecarboxylate is obtained through reaction after the stirring. The solvent is not needed in the whole reaction process; the problem of environment pollution risk caused by the use of the solvent is solved; the process belongs to a green and environment-friendly novel production process. The product and the ion liquid are filtered and are separated from inorganic salt produced through reaction and the alkali which is not completely reacted; the product is obtained through rectification. Liquid left after the rectification can be repeatedly used for the next batch of reaction; the three-waste discharge is reduced; meanwhile, the cost can be reduced; the goal of green manufacturing is achieved.

Mild, one-pot conversion of carboxylic acids into esters using phase transfer catalysis

Puntambekar, Hemalata M,Naik, D G,Kapadi, A H

, p. 793 - 794 (2007/10/02)

One-pot conversion of carboxylic acids into esters under the influence of phase transfer catalysis is reported.The method is shown to work satisfactorily for optically active acids having epimerisable α-hydrogen.

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