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2,4,6,8,10,12-Tridecahexaenoic acid, also known as (2E,4E,6E,8E,10E,12E)-2,7,11-trimethyl-13-(2,6,6-trimethyl-1-cyclohexen-1-yl)-, is a long-chain polyunsaturated fatty acid with 13 carbon atoms and six double bonds. 2,4,6,8,10,12-Tridecahexaenoic acid, 2,7,11-trimethyl-13-(2,6,6-trimethyl-1-cyclohexen-1-yl)-, (2E,4E,6E,8E,10E,12E)- is characterized by its unique structure, featuring a cyclohexene ring and three methyl groups at specific positions along the carbon chain. It is an important component in various biological systems and plays a role in cellular functions, such as membrane fluidity and signal transduction. Due to its complex structure, it is often found in specialized lipids and may have specific biological activities, although further research is needed to fully understand its role in human health and disease.

1053-30-1

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1053-30-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1053-30-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,5 and 3 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1053-30:
(6*1)+(5*0)+(4*5)+(3*3)+(2*3)+(1*0)=41
41 % 10 = 1
So 1053-30-1 is a valid CAS Registry Number.

1053-30-1SDS

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 12'-apo-β-caroten-12'-oic acid

1.2 Other means of identification

Product number -
Other names (2E,4E,6E,8E,10E,12E)-2,7,11-Trimethyl-13-(2,6,6-trimethyl-cyclohex-1-enyl)-trideca-2,4,6,8,10,12-hexaenoic acid

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:1053-30-1 SDS

1053-30-1Downstream Products

1053-30-1Relevant academic research and scientific papers

Synthesis of apocarotenoids by acyclic cross metathesis and characterization as substrates for human retinaldehyde dehydrogenases

Domínguez, Marta,Pequerul, Raquel,Alvarez, Rosana,Giménez-Dejoz, Joan,Birta, Eszter,Porté, Sergio,Rühl, Ralph,Parés, Xavier,Farrés, Jaume,de Lera, Angel R.

, p. 2567 - 2574 (2018)

A new synthesis of three apocarotenoids, namely 14′-apo-β-carotenal, 12′-apo-β-carotenal and 10′-apo-β-carotenal, has been achieved that is based on the acyclic cross-metathesis of the hexaene derived from retinal and the corresponding partners. These compounds can be enzymatically converted to their carboxylic acids by the human aldehyde dehydrogenases involved in retinaldehyde oxidation. Their kinetic parameters suggest that these enzymes might play a role in the physiological metabolism of apocarotenoids.

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