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5,9-dimethyldeca-2,4,8-trienal, also known as citral, is a naturally occurring organic compound that belongs to the class of terpenes. It is a colorless to pale yellow liquid with a strong lemon-like odor and is widely found in essential oils, particularly in lemongrass, lemon, and verbena. Citral is composed of two isomeric forms, geranial (citral A) and neral (citral B), which contribute to its characteristic aroma. 5,9-dimethyldeca-2,4,8-trienal is used extensively in the flavor and fragrance industry, particularly in the production of lemon-flavored products and as a component in various perfumes. Additionally, citral has been studied for its potential antimicrobial and anti-inflammatory properties, making it a subject of interest in the field of natural products chemistry and potential therapeutic applications.

6048-88-0

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6048-88-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6048-88-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,4 and 8 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6048-88:
(6*6)+(5*0)+(4*4)+(3*8)+(2*8)+(1*8)=100
100 % 10 = 0
So 6048-88-0 is a valid CAS Registry Number.
InChI:InChI=1/C12H18O/c1-11(2)7-6-9-12(3)8-4-5-10-13/h4-5,7-8,10H,6,9H2,1-3H3/b5-4+,12-8-

6048-88-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5,9-dimethyldeca-2,4,8-trienal

1.2 Other means of identification

Product number -
Other names 5,9-dimethyl-deca-2,4,8-trienal

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:6048-88-0 SDS

6048-88-0Relevant academic research and scientific papers

Direction of epoxidation of esters of polyunsaturated acids

Glushko,Kryshtal',Kogan,Yanovskaya

, p. 869 - 872 (1977)

The direction of the epoxidation of a number of polyunsaturated acids was studied and it was shown that the epoxidation proceeds at the double bonds furthest away from the carbethoxyl group.

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