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POLY(1,4-BUTYLENE TEREPHTHALATE) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

24968-12-5

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24968-12-5 Usage

Uses

Molded into auto parts, electrical components and domestic appliance assemblies.

Check Digit Verification of cas no

The CAS Registry Mumber 24968-12-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,9,6 and 8 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 24968-12:
(7*2)+(6*4)+(5*9)+(4*6)+(3*8)+(2*1)+(1*2)=135
135 % 10 = 5
So 24968-12-5 is a valid CAS Registry Number.

24968-12-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Polybutylene terephthalate

1.2 Other means of identification

Product number -
Other names Polybutylene terephthalate

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:24968-12-5 SDS

24968-12-5Relevant academic research and scientific papers

Preparation method of cyclic poly (butylene terephthalate) (by machine translation)

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Paragraph 0040-0049, (2020/06/02)

The invention discloses a cyclic trimetric polybutylene terephthalate preparation method. The method comprises the steps: (a) preparing bis(4-(4-allyl terephthaloyl oxy)butyl)polyethylene terephthalate (III) from bis-(4-hydroxyl butyl)-polyethylene terephthalate (I) and 4-(allyloxy carbonyl)benzoic acid (II) under action of a condensing agent and an auxiliary reagent; (b) preparing cyclic trimetric polybutylene terephthalate precursor (IV) by ring closure of the bis(4-(4-allyl terephthaloyl oxy)butyl)polyethylene terephthalate (III) under the action of a Grubbs catalyst and lewis acid; (c) hydrogenating the cyclic trimetric polybutylene terephthalate precursor under the action of Pd/C to obtain cyclic trimetric polybutylene terephthalate (V). The preparation method disclosed by the invention has the advantages that the raw materials are cheap and easy to obtain, a synthesizing route is simple and short, a yield is high, and conditions are easy to control.(The formula is shown in the description.).

Preparation method and separation method of low polymerization cyclic polymer

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Paragraph 0187-0235, (2019/11/20)

The invention provides a preparation method of a low polymerization cyclic polymer, and the method comprises the following steps: (1-1) in an organic solvent A, terephthaloyl chloride and 1,4-butanediol undergo esterification reaction under the action of

A practical synthesis of the cyclic butylene terephthalate trimer

Li, Xiaolin,Zhou, Pu,Wu, Wenxuan,Zhan, Li,Liu, Ting,Yang, Fan,Tang, Jie,Yu, Shanbao,Li, Hui,Luo, Yu

, p. 483 - 490 (2018/03/27)

This paper described a practical synthetic approach for the cyclic butylene terephthalate trimer (7). The key step was a ring-closing metathesis, using Grubbs' second-generation catalyst to form the macrocyclic ring. The advantages of this procedure included short reaction steps, simple operations and good yields.

Preparation method of cyclic tetrapolybutylene terephthalate

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Paragraph 0058; 0059; 0062; 0065; 0068, (2018/09/12)

The invention discloses a preparation method of cyclic tetrapolybutylene terephthalate. The method comprises the steps as follows: a) an initial material, namely, terephthaloyl dichloride, reacts with1,4-butanediol under the action of an alkaline reagent, and terephthalic bis(4-hydroxyl-butyl)ester, namely, a compound I, is obtained; b) the compound I reacts with monobenzyl terephthalate under the action of a condensing agent, and bis(4-(4-benzyloxy terephthaloyl)butyl)terephthalate, namely, a compound II, is obtained; c) the compound II is dissolved in a proper solvent, a catalyst is added to reduce debenzylation under the action of palladium-carbon and hydrogen, and 4,4'-[terephthaloyl bis(oxytetramethylene oxycarbonyl)]dibenzoic acid, namely a compound III, is obtained; d) the compoundIII reacts with the compound I under the action of a condensing agent, and the target product, namely, cyclic tetrapolybutylene terephthalate, is obtained. The method is low in cost, short in synthesis route, convenient to operate, high in product quality and good in industrial application value.

Cyclic polybutylene terephthalate preparation

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, (2017/07/01)

The invention specifically discloses a preparation method of novel cyclicpolybutylece terephthalate (PBT) dimer, wherein paraphthaloyl chloride and 1,4-butanediol are used as the raw materials for oriented synthesis of the cyclicpolybutylece terephthalate dimer through a protection and deprotectionstrategy, and the method is used for contrast analysis and detection of cyclicpolybutylece terephthalate dimer impurities in a PBT plastic. The chemical structural formula of the cyclicpolybutylece terephthalate dimer is described in the specification.

Polybutylene terephthalate cyclic trimerization preparation of (by machine translation)

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, (2018/01/19)

The invention specifically has described a kind of new cyclic trimeric butylene terephthalate (Cyclic PBT Dimer) method for preparing, in the terephthalic chloride and 1, the 4 the protecting [...] butanediol as raw material with oriented synthesis strategy of deprotection of the polybutylene terephthalate cyclic trimerization, in the plastics can be used for the PBT polybutylene terephthalate cyclic trimerization contrast analysis of the impurity with the detection. Said product of this invention the chemical structural formula is: (by machine translation)

Synthesis and biological evaluation of novel AM80 derivatives as antileukemic agents

Bian, Haiyong,Feng, Jinhong,Xu, Wenfang

, p. 175 - 185 (2013/03/13)

A series of novel AM80 derivatives as antileukemic agents were synthesized and their structures were confirmed by IR, 1H-NMR, and HR-MS spectra. All the target compounds were evaluated for in vitro antiproliferative activities against human leukemic HL-60, NB4, and K562 cell lines. Among these derivatives, compound 4g showed much stronger antiproliferative activities against all the three human leukemic cell lines than the positive control AM80, and compound 4b exhibited more active antiproliferative effects against HL-60 and K562 cells than AM80. Furthermore, the preliminary SAR analysis suggested that AM80 conjugating with HDAC inhibitors with small steric hindrance could give more effective antileukemic agents. These results would be helpful to design more potent antileukemic drugs for the treatment of human leukemia.

Novel antileukemic agents derived from tamibarotene and nitric oxide donors

Bian, Haiyong,Feng, Jinhong,Li, Minyong,Xu, Wenfang

, p. 7025 - 7029 (2012/01/05)

A series of novel nitric oxide-releasing tamibarotene derivatives were synthesized by coupling nitric oxide (NO) donors with tamibarotene via various spacers, and were evaluated for their antiproliferative activities against human leukemic HL-60, NB4 and

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