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N-Decyllactate, with the molecular formula C20H38O3, is a fatty acid ester that serves as a crucial component in the cosmetic and personal care industry. It is renowned for its moisturizing and softening properties, which make it an indispensable ingredient in various skincare formulations such as lotions and creams. Beyond its skincare benefits, N-Decyllactate also functions as a fragrance ingredient and exhibits antimicrobial and antibacterial properties. Recognized for its low hazard profile and minimal potential for skin irritation and sensitization, it stands out as a preferred choice for skincare product formulations.

42175-34-8

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42175-34-8 Usage

Uses

Used in Cosmetic and Personal Care Industry:
N-Decyllactate is used as an emollient and skin conditioning agent for its moisturizing and softening properties, enhancing the texture and feel of lotions, creams, and other skincare products.
Used in Fragrance Industry:
N-Decyllactate is utilized as a fragrance ingredient, contributing to the scent profiles of various personal care and cosmetic products.
Used in Antimicrobial Applications:
Due to its antimicrobial and antibacterial properties, N-Decyllactate is employed in products that require preservation and protection against microbial contamination, ensuring product safety and longevity.
Used in Skincare Formulations for Sensitive Skin:
Owing to its low potential for skin irritation and sensitization, N-Decyllactate is used in skincare products specifically designed for individuals with sensitive skin, providing gentle yet effective moisturization and conditioning.

Check Digit Verification of cas no

The CAS Registry Mumber 42175-34-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,1,7 and 5 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 42175-34:
(7*4)+(6*2)+(5*1)+(4*7)+(3*5)+(2*3)+(1*4)=98
98 % 10 = 8
So 42175-34-8 is a valid CAS Registry Number.
InChI:InChI=1/C13H26O3/c1-3-4-5-6-7-8-9-10-11-16-13(15)12(2)14/h12,14H,3-11H2,1-2H3

42175-34-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name decyl 2-hydroxypropanoate

1.2 Other means of identification

Product number -
Other names Decyl-lactat

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:42175-34-8 SDS

42175-34-8Downstream Products

42175-34-8Relevant academic research and scientific papers

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

Sathyam Reddy, Yasa,Sujitha, Pombala,Kumar, Chityal Ganesh,Kanjilal, Sanjit,Vijayalakshmi, Penumarthy

, p. 943 - 951 (2016/03/05)

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.

Natural preservatives

-

Paragraph 0088; 0089, (2016/12/26)

In the present invention, provided is a compound, which has good antibacterial effects and is denoted by general formula (I), or a pharmaceutical acceptable salt thereof where R1 is saturated or unsaturated straight chains or branch chains of an alkyl group in general formula (I); R2 is hydrogen, methyl or is selected from a general formula (2); and R3 is hydrogen, saturated or unsaturated straight chains or branch chains of an alkyl group, and X is hydrogen or is selected from a hydroxyl group in general formula (2).COPYRIGHT KIPO 2015

Development of lactic ester as bifunctional additive of methanol-gasoline

Zhang, Jie,Yang, Changchun,Tang, Ying,Xu, Lianghong,Wang, Xiaoting

, p. 4827 - 4829 (2014/12/10)

In this paper, lactic esters were synthesized and used as phase stabilizer and saturation vapor pressure depressor of methanol-gasoline. The results show that the stabilities of the methanol-gasoline depend on the length of the lactic esters' alkoxy group. Several lactic esters were found to be effective in various gasoline-methanol blends, and the lactic esters display high capacity to depress the saturation vapor pressure of methanol-gasoline. According to the results, it can be concluded that the lactic esters have the great potential to be bifunctional gasoline-methanol additives.

Compositions comprising phosphate ester compounds containing a beneficial reagent component

-

, (2008/06/13)

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.

Alkyl sulphooxyalkanoate compounds and compositions

-

, (2008/06/13)

The invention relates to novel sulfooxy alkanoates surfactants in which a portion of the surfactant molecule has a so-called "benefit reagent" function, and compositions containing these surfactants. It is believed that this benefit reagent portion comes to play when the surfactant metabolized or hydrolyzed. The surfactants used in these compositions are calcium ion insensitive, show mildness benefits and foam well. Thus the surfactants have been demonstrated to be useful surfactant in addition to delivering a beneficial reagent.

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