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3613-33-0

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3613-33-0 Usage

General Description

Octanal, 7-ethoxy-3,7-dimethyl- is a chemical compound with the molecular formula C12H24O2. It is an aldehyde with a strong, fruity odor and is commonly used as a flavoring agent in the food industry. Octanal, 7-ethoxy-3,7-dimethyl- is also known for its potent antimicrobial properties, making it a common ingredient in cleaning and personal care products. Octanal, 7-ethoxy-3,7-dimethyl- is also used in the production of perfumes and fragrances due to its pleasant aroma. Additionally, it is utilized in the synthesis of other organic compounds and plays a crucial role in various chemical and industrial processes.

Check Digit Verification of cas no

The CAS Registry Mumber 3613-33-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,1 and 3 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3613-33:
(6*3)+(5*6)+(4*1)+(3*3)+(2*3)+(1*3)=70
70 % 10 = 0
So 3613-33-0 is a valid CAS Registry Number.
InChI:InChI=1/C12H24O2/c1-5-14-12(3,4)9-6-7-11(2)8-10-13/h10-11H,5-9H2,1-4H3

3613-33-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-ethoxy-3,7-dimethyloctanal

1.2 Other means of identification

Product number -
Other names Octanal,7-ethoxy-3,7-dimethyl

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:3613-33-0 SDS

3613-33-0Downstream Products

3613-33-0Relevant articles and documents

PREPARATION OF DERIVATIVES OF CITRONELLAL

Koertvelyessy, Gyula

, p. 347 - 354 (2007/10/02)

The hydrogenation of citronellal and citral, if not separated from ethereal oils, leads regioselectively to dihydrocitronellal and citronellal, respectively.The reaction of citral with (+)-ephedrin or L-aspartic acid, followed by hydrogenation and deblocking the aldehyde function, yields optically active citronellal.Reacting the aldehyde function of citronellal with diethanolamine, piperidine or morpholine, the alcohol addition to the 6,7-double bond results in 7-alkoxy substituted citronellals with acceptable yield.The formation of 7-hydroxy-6,7-dihydrocitronellal during this reaction has been proved and the effect of reaction parameters on the yield have been discussed.

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