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CAS:539-93-5|ALPHA,ALPHA'-DILAURIN

CAS:539-93-5|ALPHA,ALPHA'-DILAURIN

Molecular Formula:C27H52O5
Molecular Weight:456.7
EINECS:208-731-9
Package:1g 5g 10g

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Introduction of CAS:539-93-5|ALPHA,ALPHA'-DILAURIN

 

 

1,3-Dilaurin can be synthesized through various chemical and enzymatic methods. For example, the synthesis of 1,3-diacylglycerols modified in the 2-position, starting from regioisomerically pure 1,3-dilauroylglycerol, involves combining enzymatic and chemical methods. The syntheses highlight the versatility and adaptability of the methods to obtain 1,3-Dilaurin derivatives with specific functional groups (Haftendorn & Ulbrich-hofmann, 1995).

 

 

The molecular structure of 1,3-Dilaurin and its derivatives has been a subject of interest, leading to studies on the crystal structures and conformational states of compounds like dilauroylphosphatidylethanolamine. These studies reveal the complex intermolecular packing and conformations within the crystalline structures, providing insights into their molecular arrangements and interactions (Hitchcock et al., 1974).

 

Specification of CAS:539-93-5|ALPHA,ALPHA'-DILAURIN

 

QUY CÁCH

74 degree

247.4±23.0 degree (Predicted)

1.07±0.1 g/cm3(Predicted)

10.89±0.10(Predicted)

 

Research Application of CAS:539-93-5|ALPHA,ALPHA'-DILAURIN

 

: 1,3-Dilaurin is synthesized for its use as a surfactant in food, cosmetics, and pharmaceutical industries. Studies explore solvent-free enzymatic synthesis methods for efficient and practical production (Zhong et al., 2013).

 

: The crystallization process of trilaurin and the impact of 1,3-Dilaurin on it is investigated for understanding crystal growth and morphology in relation to various additives (Smith, Cebula, & Povey, 1994).

 

: The effects of dibutyltin dilaurate (which includes 1,3-Dilaurin) on lipid metabolism, particularly triglyceride metabolism, are studied in liver cells. This research is crucial for understanding the compound's impact on liver function and overall health (Qiao et al., 2018).

 

: Fast pyrolysis of 1,3-Dilaurin in the presence of sodium carbonate is explored as a method for producing hydrocarbons, suggesting potential applications in biofuel production (Fonseca, Pereira, Fréty, & Sales, 2019).

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