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3-(dodecyloxy)propanoic acid, also known as 3-(dodecyloxy)propionic acid or lauric acid glyceryl ester, is a chemical compound with the molecular formula C15H30O3. It is a derivative of propanoic acid, featuring a dodecyloxy (C12H25O) group attached to the third carbon atom. This organic compound is characterized by its amphiphilic nature, possessing both hydrophilic (polar) and hydrophobic (non-polar) properties. It is commonly used in various applications, such as in the formulation of surfactants, emulsifiers, and detergents, as well as in the production of personal care and pharmaceutical products. The compound's unique structure allows it to interact with both water and oil, making it a versatile ingredient in a wide range of industrial and consumer products.

6064-81-9

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6064-81-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6064-81-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,6 and 4 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6064-81:
(6*6)+(5*0)+(4*6)+(3*4)+(2*8)+(1*1)=89
89 % 10 = 9
So 6064-81-9 is a valid CAS Registry Number.

6064-81-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-dodecoxypropanoic acid

1.2 Other means of identification

Product number -
Other names 3-dodecyloxypropanoic 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:6064-81-9 SDS

6064-81-9Downstream Products

6064-81-9Relevant academic research and scientific papers

Long-chain triazolyl acids as inhibitors of osteoclastogenesis

Marshall, Andrew J.,Lin, Jian-Ming,Grey, Andrew,Reid, Ian R.,Cornish, Jillian,Denny, William A.

, p. 4112 - 4119 (2013/07/27)

Saturated fatty acids (e.g., palmitic acid) are known to moderately inhibit the development of osteoclasts in vitro. In pursuit of more effective inhibitors of osteoclastogenesis we explored two new classes of palmitic acid analogues containing either an ether or triazolyl group at various positions along the chain. The compounds were evaluated for their ability to inhibit the formation of osteoclasts in primary mouse bone marrow cultures. The oxyacids were generally prepared by condensation of the appropriate alkyl halides and diols, followed by Jones oxidation. The triazolyl acids were prepared by copper-catalysed click chemistry between alkyl azides and acetylenic acids, or with the appropriately-protected azides and alkynes, followed by deprotection and oxidation. The oxyacids were little more effective than palmitic acid, but the triazolyl analogues were much more effective osteoclastogenesis inhibitors, especially when the triazole was distant from the acid unit.

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