Welcome to LookChem.com Sign In|Join Free

CAS

  • or

24969-06-0

Post Buying Request

24969-06-0 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

24969-06-0 Usage

Description

Resin based on epichlorohydrin and bis phenol A. Oligomers may vary in molecular weight from 340 and higher. May produce erythema multiforme like eruptions. The higher the molecular weight, the less sensitizing the compound.

Chemical Properties

Resin epoxy is white to straw slab

Uses

Different sources of media describe the Uses of 24969-06-0 differently. You can refer to the following data:
1. Resin epoxy is Surface coatings, as on household appliances and gas storage vessels; adhesive for composites and for metals, glass, and ceramics; casting metalforming tools and dies; encapsulation of electrical parts; filament-wound pipe and pressure vessels; floor surf
2. Epoxy resin is used in adhesives, surface coatings, electrical insulation, plasticizers, polymer stabilizers, laminates, surface coatings, paints and inks, product finishers, PVC products, vinyl gloves, etc.; in the building industry, electron microscopy, and sculpture.

Definition

Resin epoxy is a thermosetting resin based on the reactivity of the epoxide group. One type is made from epichlorohydrin and bisphenol A. Aliphatic polyols such as glycerol may be used instead of the aromatic bisphenol A. Molecules of this type have glycidyl ether struc

Preparation

Epoxy resin is prepared by the following condensation reaction: The condensation leaves epoxy end groups that are then reacted in a separate step with nucleophilic compounds (alcohols, acids, or amines). For use as an adhesive, the epoxy resin and the curing resin (usually an aliphatic polyamine) are packaged separately and mixed together immediately before use. Epoxy novolac resins are produced by glycidation of the low-molecular-weight reaction products of phenol (or cresol) with formaldehyde. Highly cross-linked systems are formed that have superior performance at elevated temperatures.

Hazard

Strong skin irritant in uncured state.

Check Digit Verification of cas no

The CAS Registry Mumber 24969-06-0 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 9 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 24969-06:
(7*2)+(6*4)+(5*9)+(4*6)+(3*9)+(2*0)+(1*6)=140
140 % 10 = 0
So 24969-06-0 is a valid CAS Registry Number.

24969-06-0 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Aldrich

  • (181862)  Polyepichlorohydrin  average Mw ~700,000 by GPC

  • 24969-06-0

  • 181862-100G

  • 1,104.48CNY

  • Detail

24969-06-0SDS

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 Polyepichlorohydrin

1.2 Other means of identification

Product number -
Other names epoxy resin

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:24969-06-0 SDS

24969-06-0Relevant articles and documents

Fully utilizing seeds solution for solvent-free synthesized nanosized TS-1 zeolites with efficient epoxidation of chloropropene

Chai, Yongming,Li, Bin,Li, Yichuan,Liu, Hanfang,Liu, Jia,Liu, Yanru,Ran, Saisai,Wang, Fupeng,Wang, Lei,Wang, Yu,Xie, Huijie,Ye, Tiantian

, (2021/12/27)

Nanosized titanium silicalite-1 (TS-1) demonstrates excellent catalytic ability in the selective catalytic oxidation reaction. However, their synthesis process is usually complicated with low yield under hydrothermal conditions, which is not in line with the concept of green chemistry. Herein, via fully utilizing untreated seeds solution, we report firstly an entirely green strategy for solvent-free synthesizing anatase-free nanosized TS-1 zeolite. The success lies in the fully utilization of seeds solution which is composed of supersaturated structure directing agent (TPAOH), unreacted silica source, water and formed MFI seeds (silicalite-1) without external purification. In the followed solvent-free synthesis of final nanosized TS-1 product, no additional TPAOH is added, which greatly reduces the synthesis cost and synthetic procedure and maintains a high product yield. The obtained nanosized TS-1 zeolite without anatase phase has high crystallinity, large specific surface area. More importantly, the nanosized TS-1 (Si/Ti ?= ?77) catalysts exhibit excellent catalytic ability for the epoxidation of chloropropene with 40.0% conversion and 97.6% selectivity. This sustainable and green synthesis method opens up a new way to regulate nanosized zeolite.

Selective synthesis of epichlorohydrin: Via liquid-phase allyl chloride epoxidation over a modified Ti-MWW zeolite in a continuous slurry bed reactor

Ding, Luoyi,Yin, Jinpeng,Tong, Wen,Peng, Rusi,Jiang, Jingang,Xu, Hao,Wu, Peng

, p. 331 - 342 (2021/01/11)

The epoxidation of allyl chloride (ALC) to epichlorohydrin (ECH) with H2O2 using a piperidine (PI)-modified Ti-MWW catalyst (Ti-MWW-PI) in a continuous slurry reactor was investigated to develop an efficient reaction system for the corresponding industrial process. The reaction parameters, including solvent, reaction temperature, t-butanol/ALC mass ratio, ALC/H2O2 molar ratio, weight hourly space velocity of H2O2, and the addition amount of ammonia, were studied in detail to pursue high H2O2 conversion and ECH selectivity. A long catalytic lifetime of 244 h was achieved at high H2O2 conversion (>97.0%) and ECH selectivity (>99.8%) under optimized reaction conditions. The crystallinity was well maintained for the deactivated Ti-MWW-PI catalyst, which was regenerated by a combination of calcination and piperidine treatment. This journal is

Epoxidation of Allyl Chloride in the Presence of Tungsten Oxo–Peroxo Heteropoly Compounds of P(V), As(V), and Si(IV) Under Phase-Transfer Catalysis Conditions

Panicheva,Meteleva,Ageikina,Panichev

, p. 1270 - 1274 (2021/10/20)

Abstract: This study investigates the behavior of nonmetals in tungsten oxo–peroxoheteropoly compounds in the reaction of allyl chloride epoxidation. Thecatalytic efficiency in epoxidation was shown to increase in the followingorder: Si(IV) As(V) P(V). Synergism in allyl chloride epoxidation wasdemonstrated for the first time for mixtures of tungsten oxo–peroxo heteropolycompounds of P and As, as well as P and Si. It was also shown that mixturesconsisting of 70% P + 30% Si and 75% P + 25% As exhibit the highest catalyticactivity. Finally, the article suggests a mechanism for the synergisticeffect. [Figure not available: see fulltext.].

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 24969-06-0