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29598-76-3

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  • 2,2-Bis[[3-(dodecylthio)-1-oxopropoxy]methyl]propane-1,3-diyl bis[3-(dodecylthio)propionate] Manufacturer/High quality/Best price/In stock

    Cas No: 29598-76-3

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  • Propanoic acid,3-(dodecylthio)-,1,1'-[2,2-bis[[3-(dodecylthio)-1-oxopropoxy]methyl]-1,3-propanediyl] ester 29598-76-3

    Cas No: 29598-76-3

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  • 1 Kilogram

  • 10000 Metric Ton/Month

  • Shanghai Upbio Tech Co.,Ltd
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29598-76-3 Usage

Products Recommended for

* Polyolefins (PP, PE, TPO) * Styrenic polymers (ABS, PS) * Engineering plastics (PBT, PA) * Elastomers & latex

Uses

Different sources of media describe the Uses of 29598-76-3 differently. You can refer to the following data:
1. Antioxidant412S is a high performance thioether antioxidant for the stabilization of polyolefins, styrenic polymers, and engineering plastics. Usually Antioxidant 412s is used with phenolic antioxidants so as to strengthen anti aging and light stabilities, and improve the initial color and luster.
2. 2,2-Bis[[3-(dodecylthio)-1-oxopropoxy]methyl]propane-1,3-diyl bis[3-(dodecylthio)propionate] (CAS# 29598-76-3) is an antioxidant and fatty acid derivative as a materials modifier, such as its use as a modifier for the thermal stability of polyol-ester-based thermal pastes.

Chemical Properties

White solid powder

Application

2,2-Bis[[3-(dodecylthio)-1-oxopropoxy]methyl]propane-1,3-diyl bis[3-(dodecylthio)propionate] is an antioxidant and fatty acid derivative as a materials modifier, such as its use as a modifier for the thermal stability of polyol-ester-based thermal pastes.

Flammability and Explosibility

Nonflammable

Check Digit Verification of cas no

The CAS Registry Mumber 29598-76-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,5,9 and 8 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 29598-76:
(7*2)+(6*9)+(5*5)+(4*9)+(3*8)+(2*7)+(1*6)=173
173 % 10 = 3
So 29598-76-3 is a valid CAS Registry Number.
InChI:InChI=1/C65H124O8S4/c1-5-9-13-17-21-25-29-33-37-41-49-74-53-45-61(66)70-57-65(58-71-62(67)46-54-75-50-42-38-34-30-26-22-18-14-10-6-2,59-72-63(68)47-55-76-51-43-39-35-31-27-23-19-15-11-7-3)60-73-64(69)48-56-77-52-44-40-36-32-28-24-20-16-12-8-4/h5-60H2,1-4H3

29598-76-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name [3-(3-dodecylsulfanylpropanoyloxy)-2,2-bis(3-dodecylsulfanylpropanoyloxymethyl)propyl] 3-dodecylsulfanylpropanoate

1.2 Other means of identification

Product number -
Other names Tetrakis(2-methoxyethoxy)silane

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Processing aids, not otherwise listed
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:29598-76-3 SDS

29598-76-3Downstream Products

29598-76-3Relevant articles and documents

Method for synthesizing pentaerythritol tetra (3-lauryl thiopropionate) by one-pot method

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Paragraph 0023; 0025-0040, (2021/08/21)

The invention provides a method for synthesizing pentaerythritol tetra (3-lauryl thiopropionate) by a one-pot process. The method comprises the following steps: adding a reaction solvent into a reaction container, then sequentially adding pentaerythritol, acrylic acid, triethylamine and catalytic equivalent strong base, heating to 55 DEG C, slowly dropwise adding dodecanethiol, keeping the temperature for 2 hours, slowly dropwise adding a reaction solution in which triphosgene is dissolved, and carrying out heat preservation and stirring for 2 hours after dropwise adding is completed; and after the reaction is finished, washing with water, removing the solvent, and crystallizing and separating to obtain the product. According to the invention, the method has the characteristics of low raw material cost, mild reaction conditions, high reaction speed, simplicity in operation, less pollution and environmental friendliness; and compared with the high-temperature reaction conditions required for synthesizing pentaerythritol tetra (3-lauryl thiopropionate) by a transesterification method or esterification method, the energy consumption is effectively reduced, the production time is shortened, the production efficiency is improved, and the method is suitable for industrial production.

A four-(3 - dodecyl sulfur generation of propionic acid) pentaerythritol method for preparing an antioxidant (by machine translation)

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Paragraph 0042-0047, (2018/09/08)

The invention discloses a four-(3 - dodecyl sulfur generation of propionic acid) pentaerythritol method for preparing an antioxidant. This kind of preparation method comprises the following steps: 1) will be an azo compound is can be mixed, heated to 60 °C -85 °C, adding 3 - mercapto propionic acid, stirring reaction; 2) heating up to 100 °C -120 °C, adding pentaerythritol and acidic catalyst mixed solution, mixed reaction; 3) the solid product through the purification reaction, drying, to obtain four (3 - dodecyl sulfur generation of propionic acid) pentaerythritol. This preparation method using the medium acidic catalyst, the advantages that the high reaction activity, good dispersibility, the price is cheap. The reaction technology is moderate, not easily cause equipment corrosion, simple operation, high selectivity catalyst product, product is light in color. At the same time the esterification reaction using a mixed solvent, to pentaerythritol has excellent dissolution effect, to ensure that the reaction has been in a homogeneous system, the reaction efficiency is improved and the product yield. (by machine translation)

Stabilizer for synthetic resins

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, (2008/06/13)

Synthetic resins, particularly polyolefins, are markedly improved in their resistances to heat and oxidation by the incorporation of a 2-methyl-4-t-butyl-5-hydroxyphenylalkanoic acid ester alone or in combination with a thioether-type antioxidant represented by the general formula STR1 wherein R represents an alkyl group of 12 to 20 carbon atoms, or by the general formula STR2 wherein R represents an alkyl group of 4 to 20 carbon atoms.

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