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2-Chloroethyl palmitate is an organic compound with the chemical formula C13H27ClO2. It is a derivative of palmitic acid, where a 2-chloroethyl group replaces the hydrogen atom at the second carbon position. This chlorinated ester is used as a chemical intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of alkylating agents. It is also employed in the manufacturing of surfactants and as a solvent in some industrial processes. Due to its reactivity, 2-chloroethyl palmitate requires careful handling and is typically stored under controlled conditions to prevent unwanted reactions.

929-16-8

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929-16-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 929-16-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,2 and 9 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 929-16:
(5*9)+(4*2)+(3*9)+(2*1)+(1*6)=88
88 % 10 = 8
So 929-16-8 is a valid CAS Registry Number.
InChI:InChI=1/C18H35ClO2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-18(20)21-17-16-19/h2-17H2,1H3

929-16-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chloroethyl hexadecanoate

1.2 Other means of identification

Product number -
Other names 2-chloro-1-ethyl palmitate

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:929-16-8 SDS

929-16-8Downstream Products

929-16-8Relevant academic research and scientific papers

Zinc-catalyzed depolymerization of polyethers to produce valuable building blocks

Enthaler, Stephan

, p. 850 - 859 (2014/06/23)

The recycling of polymers continues to be a significant matter for a sustainable society. In particular, the conversion of end-of-life polymers to monomers or suitable low-molecular weight chemicals creates a feedstock for new high-quality polymeric materials and contributes to conserve resources and allow overall an efficient waste-managing system. In the present study, we have set up a straightforward methodology for the depolymerization of artificial polyethers applying cheap and abundant zinc( II) salts as precatalysts. In the presence of bio-based fatty acid chlorides as depolymerization reagent well-defined chloroesters were accessible in good to excellent yields. Moreover, acetic anhydride and fatty acids were applied as depolymerization reagents resulting in the formation of diacetates in moderate yields. In both cases the obtained products (chloroesters, diacetates) can be useful building blocks in polymerization chemistry. Noteworthy, overall a recycling of polyethers are possible. Springer Science+Business Media New York 2014.

Cationic imidazolium monomeric surfactants: Their synthesis and surface active properties

Ahmad, Ishtiaque,Patial, Pankaj,Kaur, Charanjeet,Kaur, Satindar

, p. 269 - 277 (2014/03/21)

A series of long-chain ester-based water-soluble cationics have been synthesized by using renewable raw materials like fatty acids and halogenated alcohols. The surface activity of the molecules has been determined by measurement of their conductance and surface tension in aqueous solution. The dynamics of surface activity of these surfactants have also been investigated in the presence of sodium halides (NaCl and NaBr) by surface tension measurement. A series of useful parameters like critical micelle concentration (CMC), surface tension at the CMC (γCMC), adsorption efficiency (pC 20), effectiveness of surface tension reduction (ΠCMC), Gibbs free energy of the micellization (ΔG0mic) and Gibbs free energy of adsorption (ΔG0ads) have been determined from the measurements obtained by surface tension and conductivity methods. Further with the application of the Gibbs adsorption isotherm, maximum surface excess concentration (Γmax) and minimum surface area/molecule (A min) at the air-water interface were also estimated. Thermal stability of these long chain cationics have been measured by thermal gravimetric analysis under a nitrogen atmosphere. Analysis of thermal stability measurement indicated that the thermal stability of these long chain imidazoliums increases with an increase in chain length.

Gemini pyridinium surfactants: Synthesis and their surface active properties

Patial, Pankaj,Shaheen, Arifa,Ahmad, Ishtiaque

, p. 929 - 935 (2014/09/30)

New pyridinium Gemini surfactants have been synthesized by esterification of renewable fatty acids with halogenated alcohols furnishing respective esters (2-chloroethyl hexadecanoate, 2-chloroethyl tetradecanoate, 2-chloroethyl dodecanoate, 2-bromoethyl hexadecanoate, 2-bromoethyl tetradecanoate and 2-bromoethyl dodecanoate) followed by their subsequent treatment with 4,4′-trimethylenedipyridine resulting into the formation of title Gemini surfactants: (4,4′-(propane-1,3-diyl)bis(1-(2-(hexadecanoyl oxy) ethyl) dipyridinium chloride(7), (4,4′-(propane-1,3-diyl)bis(1-(2-(tetradecanoyl oxy) ethyl) dipyridinium chloride (8), 4,4′-(propane-1,3-diyl)bis(1-(2- (dodecanoyl oxy) ethyl) dipyridinium chloride (9), (4,4′-(propane-1,3- diyl)bis(1-(2-(hexadecanoyl oxy) ethyl) dipyridinium bromide (10), (4,4′-(propane-1,3-diyl)bis(1-(2-(tetradecanoyl oxy) ethyl) dipyridinium bromide (11), 4,4′-(propane-1,3-diyl)bis(1-(2-(dodecanoyl oxy) ethyl) dipyridinium bromide (12). Their identifications are based on IR, 1H-, 13C-NMR, DEPT, COSY and mass spectral studies. Their surface active properties are also evaluated on the basis of surface tension and conductivity measurements and thermal stability of these long chain cationics Gemini surfactants have been measured by thermal gravimetric analysis under nitrogen atmosphere.

Sustained release pharmaceutical compositions

-

Page/Page column 7, (2008/06/13)

The present invention relates to a pharmaceutical composition comprising a salt of quaternary ammonium of an acid drug in the form of a suspension or an emulsion, suitable for parenteral administration and providing a sustained release of the drug. In one preferred embodiment, the present invention is directed to a long term sustained release composition for parenteral administration, comprising a salt of heparin or low molecular weight heparin in an emulsion with a salt of acylcholine, for the prevention and treatment of venous thrombosis and pulmonary embolism.

Esters, retroesters, and a retroamide of palmitic acid: Pool for the first selective inhibitors of N-palmitoylethanolamine-selective acid amidase

Vandevoorde, Séverine,Tsuboi, Kazuhito,Ueda, Natsuo,Jonsson, Kent-Olov,Fowler, Christopher J.,Lambert, Didier M.

, p. 4373 - 4376 (2007/10/03)

Cyclohexyl hexadecanoate, hexadecyl propionate, and N-(3-hydroxypropionyl)pentadecanamide, respectively ester, retroester, and retroamide derivatives of N-palmitoylethanolamine, represent the first selective inhibitors of "N-palmitoylethanolamine hydrolase" described so far. These compounds are devoid of affinity for CB1 and CB 2 receptors and characterized by high percentages of inhibition of N-palmitoylethanolamine-selective acid amidase (84.0, 70.5, and 76.7% inhibition at 100 μM, respectively) with much lower inhibitory effect on either fatty acid amide hydrolase or the uptake of anandamide.

Chlorotrimethylsilane: A suitable reagent for the synthesis of chlorohydrin esters

Eras, Jordi,Mendez, Jonh Jairo,Balcells, Merce,Canela, Ramon

, p. 8631 - 8634 (2007/10/03)

A new methodology for obtaining chlorohydrin esters using a one-pot esterification-chlorination reaction, in which one of the reagents, chlorotrimethylsilane, acts as solvent, is described. The reaction is stereospecific and its regioselectivity depends o

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