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1-(1-glycero)dodeca-1,3,5,7,9-pentaene is a complex polyunsaturated hydrocarbon belonging to the glycerolipids family, which are vital components of cell membranes. This chemical compound features twelve carbon atoms and five double bonds, endowing it with a long, flexible structure. Its high reactivity, due to the multiple double bonds, positions it as a promising candidate for pharmaceuticals, organic synthesis, and materials science. Additionally, similar compounds have demonstrated anti-inflammatory and antioxidative properties, suggesting potential utility in drug and health supplement development.

84000-59-9

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84000-59-9 Usage

Uses

Used in Pharmaceutical Applications:
1-(1-glycero)dodeca-1,3,5,7,9-pentaene is used as an active pharmaceutical ingredient for its potential anti-inflammatory and antioxidative properties, which can be harnessed in the development of new drugs and health supplements.
Used in Organic Synthesis:
In the field of organic synthesis, 1-(1-glycero)dodeca-1,3,5,7,9-pentaene is used as a key intermediate compound for the synthesis of various complex molecules, leveraging its high reactivity and unique structural features.
Used in Materials Science:
1-(1-glycero)dodeca-1,3,5,7,9-pentaene is utilized as a component in the development of novel materials, capitalizing on its reactive nature and structural flexibility to create advanced materials with specific properties for various applications.
Used in Research and Development:
In the research and development industry, 1-(1-glycero)dodeca-1,3,5,7,9-pentaene serves as a model compound for studying the effects of polyunsaturation on molecular behavior and reactivity, furthering scientific understanding and potentially leading to innovative applications in multiple fields.

Check Digit Verification of cas no

The CAS Registry Mumber 84000-59-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,0,0 and 0 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 84000-59:
(7*8)+(6*4)+(5*0)+(4*0)+(3*0)+(2*5)+(1*9)=99
99 % 10 = 9
So 84000-59-9 is a valid CAS Registry Number.
InChI:InChI=1/C15H22O3/c1-2-3-4-5-6-7-8-9-10-11-12-18-14-15(17)13-16/h3-12,15-17H,2,13-14H2,1H3/b4-3+,6-5+,8-7+,10-9+,12-11+

84000-59-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-[(1E,3E,5E,7E,9E)-dodeca-1,3,5,7,9-pentaenoxy]propane-1,2-diol

1.2 Other means of identification

Product number -
Other names Fecapentaene-12

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:84000-59-9 SDS

84000-59-9Downstream Products

84000-59-9Relevant academic research and scientific papers

Acid-catalyzed solvolysis of polyenol ethers. II. Effect of the degree of unsaturation

Vertegaal,Van Der Gen

, p. 7301 - 7312 (2007/10/02)

The acid-catalyzed solvolysis of polyenol ethers of glycerol gradually changes with increasing unsaturation from the regular pattern into an anomalous one in which hydroxy- and methoxy-substituted aldehydes are formed.

SYNTHESIS OF RACEMIC FECAPENTAENE-12, A POTENT MUTAGEN FROM HUMAN FECES, AND ITS REGIOISOMER

Gunatilaka, A. A. Leslie,Hirai, Nobuhiro,Kingston, David G. I.

, p. 5457 - 5460 (2007/10/02)

Racemic fecapentaene-12 and its regioisomer 2-(1,3,5,7,9-dodecapentaenyloxy)-1,3-propanediol (2) have been synthesized.The latter compound is comparably mutagenic to 1.

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