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3454-29-3

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  • Oxirane, 2,2'-[[2-ethyl-2-[(2-oxiranylmethoxy)methyl]-1,3-propanediyl]bis(oxymethylene)]bis-

    Cas No: 3454-29-3

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3454-29-3 Usage

Uses

Trimethylolpropane Triglycidyl Ether is used in method for producing pharmaceutical filler complex.

Check Digit Verification of cas no

The CAS Registry Mumber 3454-29-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,5 and 4 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 3454-29:
(6*3)+(5*4)+(4*5)+(3*4)+(2*2)+(1*9)=83
83 % 10 = 3
So 3454-29-3 is a valid CAS Registry Number.
InChI:InChI=1/C15H26O6/c1-2-15(9-16-3-12-6-19-12,10-17-4-13-7-20-13)11-18-5-14-8-21-14/h12-14H,2-11H2,1H3

3454-29-3 Well-known Company Product Price

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  • Aldrich

  • (430269)  Trimethylolpropanetriglycidylether  technical grade

  • 3454-29-3

  • 430269-250ML

  • 687.96CNY

  • Detail
  • Aldrich

  • (430269)  Trimethylolpropanetriglycidylether  technical grade

  • 3454-29-3

  • 430269-1L

  • 2,082.60CNY

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3454-29-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[2,2-bis(oxiran-2-ylmethoxymethyl)butoxymethyl]oxirane

1.2 Other means of identification

Product number -
Other names EINECS 222-384-0

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:3454-29-3 SDS

3454-29-3Downstream Products

3454-29-3Relevant articles and documents

BIO-NANO POWER CELLS AND THEIR USES

-

, (2014/01/08)

The present invention concerns bio-nano power cells and methods of their manufacture and use. More particularly, the present invention relates to the preparation of bio-nano power cells that are biocompatible and capable of producing flash, intermittent, or continuous power by electrolyzing compounds in biological systems.

Dendritic polymers with enhanced amplification and interior functionality

-

, (2011/08/03)

Poly(ester-acrylate) and poly(ester/epoxide) dendrimers. These materials can be synthesized by utilizing the so-called “sterically induced stoichiometric” principles. The preparation of the dendrimers is carried out by reacting precursor amino/polyamino-functional core materials with various branch cell reagents. The branch cell reagents are dimensionally large, relative to the amino/polyamino-initiator core and when reacted, produce generation=1 dendrimers directly in one step. There is also a method by which the dendrimers can be stabilized and that method is the reaction of the dendrimers with surface reactive molecules to pacify the reactive groups on the dendrimers.

A facile synthesis of polyglycidyl ethers from polyols and epichlorohydrin

Kida,Yokota,Masuyama,Nakatsuji,Okahara

, p. 487 - 489 (2007/10/02)

The reaction of 1,1,1-tris(hydroxymethyl)ethane (1a), 2-ethyl-2-(hydroxymethyl)-1,3-propanediol (1b), pentaerythritol (1c), or 1,2,6-hexanetriol (1e) with epichlorohydrin in the presence of potassium hydroxide in dimethyl sulfoxide gave the corresponding tri- or tetraglycidyl ethers 3a-c, e in high yields. This procedure was also applicable to the preparation of the phenolic polyglycidyl ethers.

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