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7445-47-8

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7445-47-8 Usage

Chemical Properties

Yellow Liquid

Uses

Pentaerythritol Tetrahexanoate (cas# 7445-47-8) is a compound useful in organic synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 7445-47-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,4 and 5 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 7445-47:
(6*7)+(5*4)+(4*4)+(3*5)+(2*4)+(1*7)=108
108 % 10 = 8
So 7445-47-8 is a valid CAS Registry Number.
InChI:InChI=1/C29H52O8/c1-5-9-13-17-25(30)34-21-29(22-35-26(31)18-14-10-6-2,23-36-27(32)19-15-11-7-3)24-37-28(33)20-16-12-8-4/h5-24H2,1-4H3

7445-47-8SDS

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 PENTAERYTHRITOL TETRAHEXANOATE

1.2 Other means of identification

Product number -
Other names tetra-O-hexanoyl-pentaerythritol

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:7445-47-8 SDS

7445-47-8Relevant articles and documents

Retention Indices and Sorption Enthalpies of Pentaerythritol and С2–С8 Acid Esters on Nonpolar Stationary Phases

Emel’yanov, V. V.,Krasnykh, E. L.,Portnova, S. V.

, p. 2168 - 2176 (2020/10/08)

Abstract: The retention and sorption enthalpy characteristics of 38 pentaerythritol esters of C2–C8 carboxylic acids of different structures were determined by gas-liquid chromatography on a nonpolar phase in the temperature range 433.2–563.2 K. The molecular structure was shown to affect the temperature dependence of the retention indices of the esters. The average change in the sorption enthalpy of pentaerythritol tetraesters per CH2 group is lower in magnitude than the similar contribution for normal alkanes. The excess mixing enthalpy at 298.2 K was evaluated for four fully substituted pentaerythritol esters.

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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