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15834-04-5

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15834-04-5 Usage

Description

2,2-bis[[(1-oxopentyl)oxy]methyl]propane-1,3-diyl divalerate, also known as Pentaerythritol Tetrapentanoate, is a synthetic organic compound that belongs to the class of esters. It is characterized by its molecular structure, which consists of a propane-1,3-diyl backbone with two pentanoate ester groups attached to the 2,2-bis positions. This unique structure endows it with specific properties that make it suitable for various applications in different industries.

Uses

Used in Plastic Industry:
2,2-bis[[(1-oxopentyl)oxy]methyl]propane-1,3-diyl divalerate is used as an ester plasticizer for polymers, specifically for polyvinyl chloride (PVC). Its compatibility with PVC and ability to enhance the flexibility and workability of the polymer make it a valuable additive in the plastic industry.
Used in Lubricant Industry:
In the lubricant industry, 2,2-bis[[(1-oxopentyl)oxy]methyl]propane-1,3-diyl divalerate is utilized as a four polyol ester-based lubricant. Its ester functionality and viscosity characteristics contribute to improved lubrication properties, making it an effective additive for various applications requiring reduced friction and wear.
Different applications in different industries can be listed as follows:
Used in Plastic Industry:
2,2-bis[[(1-oxopentyl)oxy]methyl]propane-1,3-diyl divalerate is used as an ester plasticizer for PVC to improve its flexibility and workability.
Used in Lubricant Industry:
2,2-bis[[(1-oxopentyl)oxy]methyl]propane-1,3-diyl divalerate is used as a four polyol ester-based lubricant to enhance the lubrication properties and reduce friction and wear in various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 15834-04-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,8,3 and 4 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 15834-04:
(7*1)+(6*5)+(5*8)+(4*3)+(3*4)+(2*0)+(1*4)=105
105 % 10 = 5
So 15834-04-5 is a valid CAS Registry Number.
InChI:InChI=1/C25H44O8/c1-5-9-13-21(26)30-17-25(18-31-22(27)14-10-6-2,19-32-23(28)15-11-7-3)20-33-24(29)16-12-8-4/h5-20H2,1-4H3

15834-04-5SDS

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 [3-pentanoyloxy-2,2-bis(pentanoyloxymethyl)propyl] pentanoate

1.2 Other means of identification

Product number -
Other names 2,2-Bis(((1-oxopentyl)oxy)methyl)-1,3-propanediyl pentanoate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Lubricants and lubricant additives
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:15834-04-5 SDS

15834-04-5Downstream Products

15834-04-5Relevant articles and documents

Solubility of HFC32, HFC125, HFC134a, HFC143a, and HFC152a in a pentaerythritol tetrapentanoate ester

Wahlstroem, Asa,Vamling, Lennart

, p. 823 - 828 (1999)

Solubilities of five different hydrofluorocarbons (HFCs) in a pentaerythritol tetrapentanoate ester (95% purity) have been measured at temperatures between 303.15 and 363.15 K and pressures between 0.05 and 1.9 MPa. Henry's constant and the activity coefficient for HFCs at infinite dilution were derived for measurements below 0.26 MPa. The measurements were made with an isochoric method with an uncertainty of less than 2% for Henry's constant and less than 3% at high pressure. Within the investigated temperature range, solubilities for HFCs decrease in the following order: HFC152a > HFC134a > HFC32 > HFC125 > HFC143a. The experimental data have been correlated with a Flory-Huggins model with an extended temperature dependence, which is able to describe the data with a deviation from measured data of less than 2%.

An efficient catalyst COK-15b for the catalytic synthesis of lubricating ester oils

Wang, Yanan,Ma, Rui,Jiang, Cheng,Lou, Wenjing,Wang, Xiaobo

, p. 28 - 32 (2019/01/24)

The new material MOF of (CTA)1/3[Cu46(C9H3O6)24(OH)12] (PW12O40)3·xH2O (COK-15b) was synthesized via a dual-templating approach and exhibited high activity and selectivity for the esterification of pentaerythrotol with fatty acids at stoichiometric ratio to the corresponding pentaerythrotol tetra-esters with up to 98% yields under solvent-free conditions. The COK-15b was characterized by TEM, SEM, TG, BET, TPD and Py-IR. Moreover, the stability of COK-15b was investigated, and it can be reused for 5 running cycles without significant deactivation.

Microwave-promoted synthesis of polyol esters for lubrication oil using a composite catalyst in a solvent-free procedure

Zhang, Fengxiu,Zhang, Guangxian

experimental part, p. 178 - 184 (2011/03/23)

A rapid, highly efficient and green synthetic approach to polyol esters for lubrication oils is proposed. Using sulfuric acid and p-toluene sulfonic acid as a composite catalyst and C5-C9 straight-chain monocarboxylic acids, with pentaerythritol (PE) and dipentaerythritol (di-PE) as starting materials, a series of lubrication oil polyol esters were synthesized in the absence of solvent under microwave irradiation. Compared with the conventional synthetic method, our proposed microwave method exhibits advantages, including higher yields, shorter reaction times and lower reaction temperatures. The viscosity coefficients of the products at 40 °C and their refractive indices at 25 °C were investigated. In addition, the thermal behavior of the starting materials under microwave irradiation was also investigated. The results reveal that the microwave absorbance of n-pentanoic acid is stronger than that of n-hexanoic acid and that of n-heptanoic acid is stronger than that of n-octanoic acid. The microwave absorbance of di-PE is also stronger than that of PE.

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