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1195233-59-0

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1195233-59-0 Usage

General Description

Ethyllucidone, also known as ethyl 3-(3,5-dimethyl-4-hydroxyphenyl)propanoate, is a chemical compound commonly used in the fragrance and flavor industry. It is a synthetic aromatic ester with a sweet, floral, and fruity scent, often used in perfumes, soaps, and other personal care products. Ethyllucidone exhibits antioxidant properties and is commonly added to cosmetic formulations to prevent rancidity and oxidation of oils and fats. It is also used in food products to enhance their aroma and flavor. Overall, ethyllucidone is a versatile compound that contributes to the sensory appeal and stability of various consumer products.

Check Digit Verification of cas no

The CAS Registry Mumber 1195233-59-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,5,2,3 and 3 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1195233-59:
(9*1)+(8*1)+(7*9)+(6*5)+(5*2)+(4*3)+(3*3)+(2*5)+(1*9)=160
160 % 10 = 0
So 1195233-59-0 is a valid CAS Registry Number.

1195233-59-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (2E)-2-[(2E)-1-Ethoxy-3-phenyl-2-propen-1-ylidene]-4-methoxy-4-cy clopentene-1,3-dione

1.2 Other means of identification

Product number -
Other names -

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:1195233-59-0 SDS

1195233-59-0Upstream product

1195233-59-0Downstream Products

1195233-59-0Relevant articles and documents

Studies on the constituents of Lindera erythrocarpa Makino. II. Mass spectrometry of the falvonoids from the fruits (author's transl)

Liu,Takai,Ogihara

, p. 511 - 518,513,517 (2007/10/06)

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