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2-Methoxyethyl palmitate, with the molecular formula C20H40O3, is a versatile ester compound derived from palmitic acid and methoxyethyl alcohol. It is recognized for its multifunctional properties, including its role as an emollient, thickening agent, lubricant, and solvent. Its low volatility and good stability contribute to its wide range of applications across various industries.

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  • 111-07-9 Structure
  • Basic information

    1. Product Name: 2-methoxyethyl palmitate
    2. Synonyms: 2-methoxyethyl palmitate;Hexadecanoic acid 2-methoxyethyl ester
    3. CAS NO:111-07-9
    4. Molecular Formula: C19H38O3
    5. Molecular Weight: 314.50322
    6. EINECS: 203-830-3
    7. Product Categories: N/A
    8. Mol File: 111-07-9.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 394.6°Cat760mmHg
    3. Flash Point: 141.8°C
    4. Appearance: /
    5. Density: 0.893g/cm3
    6. Vapor Pressure: 1.96E-06mmHg at 25°C
    7. Refractive Index: 1.444
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 2-methoxyethyl palmitate(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-methoxyethyl palmitate(111-07-9)
    12. EPA Substance Registry System: 2-methoxyethyl palmitate(111-07-9)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 111-07-9(Hazardous Substances Data)

111-07-9 Usage

Uses

Used in Cosmetic and Personal Care Industry:
2-Methoxyethyl palmitate is used as an emollient and thickening agent for its moisturizing and skin conditioning properties. It is particularly valued in the formulation of lotions, creams, and other skincare products due to its ability to improve the texture and feel of these products on the skin.
Used in Industrial Applications:
In industrial settings, 2-Methoxyethyl palmitate serves as a lubricant and solvent. Its low volatility and good stability make it suitable for use in various processes where a stable and non-volatile compound is required to facilitate movement or dissolve substances.

Check Digit Verification of cas no

The CAS Registry Mumber 111-07-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,1 and 1 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 111-07:
(5*1)+(4*1)+(3*1)+(2*0)+(1*7)=19
19 % 10 = 9
So 111-07-9 is a valid CAS Registry Number.
InChI:InChI=1/C19H38O3/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-19(20)22-18-17-21-2/h3-18H2,1-2H3

111-07-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methoxyethyl hexadecanoate

1.2 Other means of identification

Product number -
Other names EINECS 203-830-3

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:111-07-9 SDS

111-07-9Downstream Products

111-07-9Relevant articles and documents

Synthesis of ethylene glycol monomethyl ether monolaurate catalysed by KF/NaAlO2 as a novel and efficient solid base

Lou, Shengfeng,Jia, Lihua,Guo, Xiangfeng,Wu, Wenwang,Gao, Lianbing,Wu, Hongyuan,Wang, Jianjun

, p. 6921 - 6931 (2016/07/13)

A novel solid base catalyst of NaAlO2 modified with KF (x-KF/NaAlO2) was prepared using a wet-impregnation method and used for the synthesis of ethylene glycol monomethyl ether monolaurate (EGMEML) via transesterification of ethylene glycol monomethyl ether (EGME) and methyl laurate (ML). The catalyst was characterized using the Hammett indicator method, X-ray diffraction, thermogravimetric analysis, Fourier transform infrared spectroscopy, and scanning electron microscopy with an energy dispersive spectrometer. The effect of the reaction parameters such as the amount of KF loading, molar ratio of EGME to ML, dosage of the catalyst, reaction time and temperature on the yield of EGMEML was investigated. These characterizations led to a conclusion that the reaction between NaAlO2 and KF mainly generates fluoroaluminates, which act as the main active sites for the transesterification. The catalyst shows excellent catalytic activity and good stability. The highest yield of 91% was obtained over 30%-KF/NaAlO2 at an EGME/ML molar ratio of 3.0, a catalyst amount of 5 wt%, and a reaction time of 4 h at 120 °C. A yield of 80% was obtained after use for three consecutive rounds without reactivation. Furthermore, a desirable yield of 88.0% of a novel biodiesel of ethylene glycol methyl ether soybean oil monoester was obtained with 30%-KF/NaAlO2 as a catalyst. Moreover, it was found that the reaction follows second-order kinetics, the activation energy (Ea) of the reaction of EGME with ML equals 56.54 kJ mol-1, and the thermodynamic parameters of activation were evaluated based on an activation complex theory of the reaction, and the following data were obtained: ΔG? > 0, ΔH? > 0 and ΔS? 0, indicating the unspontaneous and endergonic nature of the reaction of EGME with ML. A Koros-Nowak test was conducted and the results confirmed that the diffusion limitations did not affect the catalytic activity. Finally, a few of the physicochemical properties of the EGMEML as biodiesel were determined, and the values were within those of European standards.

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