6283-92-7

Basic information

• Product Name: LAURYL LACTATE
• Synonyms: 2-hydroxy-propanoicacidodecylester;2-hydroxy-propionicaciddodecylester;Dodecyllactate;Propanoicacid,2-hydroxy-,dodecylester;2-hydroxy-propanoic acid dodecyl ester;Lactic Acid Dodecyl Ester;Ceraphyl 31;Chrystap HYL 98
• CAS NO: 6283-92-7
• Molecular Formula: C₁₅H₃₀O₃
• Molecular Weight: 258.3969
• EINECS: 228-504-8
• Product Categories: Aliphatics;Fatty Acid Derivatives & Lipids;Glycerols
• Mol File: 6283-92-7.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 341.65°C (rough estimate)
• Flash Point: 133.1 °C
• Appearance: /
• Density: 1.0329 (rough estimate)
• Vapor Pressure: 8.5E-05mmHg at 25°C
• Refractive Index: 1.4500 (estimate)
• PKA: 13.05±0.20(Predicted)
• Water Solubility: 0.1g/L(25 oC)
• CAS DataBase Reference: LAURYL LACTATE(CAS DataBase Reference)
• NIST Chemistry Reference: LAURYL LACTATE(6283-92-7)
• EPA Substance Registry System: LAURYL LACTATE(6283-92-7)

Safety Data

• Hazardous Substances Data: 6283-92-7(Hazardous Substances Data)

Usage

Uses

An α-alkyl lactate, Lactic Acid Dodecyl Ester can be used in nanoemulsions for treating fungal, yeast and mold infections.

InChI:InChI=1/C15H30O3/c1-3-4-5-6-7-8-9-10-11-12-13-18-15(17)14(2)16/h14,16H,3-13H2,1-2H3

Upstream product

• 97-64-3 ethyl 2-hydroxypropionate 
• 112-53-8 1-dodecyl alcohol 
• 547-64-8 methyl lactate 
• 849585-22-4 LACTIC ACID 
• 814-80-2 calcium lactate 
• 312-85-6 sodium lactate 

Relevant articles and documents

Synthesis and Evaluation of Surface and Biological Properties of Some Lactic Acid-Based Anionic Surfactants

In the present study, 11 lactic acid-based anionic surfactants were synthesized and evaluated for their surface and biological activities. The synthesis involved the esterification of lactic acid with a range of fatty alcohols differing in chain length as well as in branching and unsaturation. The resultant ester was sulfonated by treatment with chlorosulfonic acid followed by salt formation with aqueous NaOH solution. The surface properties of all the synthesized surfactants were determined using surface tensiometry. Synthesized surfactants showed low critical micelle concentration (CMC) values and a decreasing trend with an increase in the alkyl chain length. Alkyl branching also led to a mild change in CMC values when compared with linear counterparts having the same number of carbon atoms, though such decreases or increases were observed to be dependent on the position and number of the branching. Some of the synthesized surfactants exhibited good antimicrobial and anti-cancer activities against the tested microbial strains and cell lines.

SKIN EXTERNAL PREPARATIONS AND COSMETICS

An object of the present invention is to provide skin external preparations and cosmetics which contain a branched acyl carnitine and have excellent formulation stability. A skin external preparation of the present invention includes a carnitine derivative represented by the following Formula (1) and/or a carnitine derivative salt represented by the following Formula (2), and an amphoteric surfactant. In Formula (1), R1 and R2 are each independently a C1-18 optionally branched, saturated or unsaturated aliphatic hydrocarbon group. In Formula (2), R1 and R2 are the same as in Formula (1), X? is a specific anion and Y+ is a specific cation.

Compositions comprising phosphate ester compounds containing a beneficial reagent component

The invention relates to novel compositions, in particular personal product compositions containing phosphate ester surfactants in which a portion of the surfactant molecule has a so-called "benefit reagent" function. It is believed that this benefit reagent portion comes to play when the surfactant is metabolized or hydrolyzed.