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1,1,4,4-Tetraisopropyl-2-butyne-1,4-diol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

6289-25-4

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6289-25-4 Usage

Functional groups

Contains two hydroxyl functional groups

Type of compound

Diol

Common uses

a. Crosslinking agent in rubber and polymer production
b. Stabilizer and inhibitor in industrial processes

Strength and elasticity

Improves the strength and elasticity of rubber and other polymers

Toxicity

Low toxicity

Stability

High stability

Industrial applications

Considered safe and effective for various industrial applications

Check Digit Verification of cas no

The CAS Registry Mumber 6289-25-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,8 and 9 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6289-25:
(6*6)+(5*2)+(4*8)+(3*9)+(2*2)+(1*5)=114
114 % 10 = 4
So 6289-25-4 is a valid CAS Registry Number.
InChI:InChI=1/C16H30O2/c1-11(2)15(17,12(3)4)9-10-16(18,13(5)6)14(7)8/h11-14,17-18H,1-8H3

6289-25-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,7-dimethyl-3,6-di(propan-2-yl)oct-4-yne-3,6-diol

1.2 Other means of identification

Product number -
Other names 3,6-Diisopropyl-2,7-dimethyl-oct-4-in-3,6-diol

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:6289-25-4 SDS

6289-25-4Downstream Products

6289-25-4Relevant academic research and scientific papers

Sterically Hindered Double Bond Systems, 2. - On the Preparation of Highly Substituted 1,3-Dienes

Hopf, Henning,Lipka, Helmut

, p. 2075 - 2084 (2007/10/02)

Highly alkylated 1,3-dienes may be prepared by treatment of 2-butyne-1,4-diol derivatives with organocuprates in good yield.Thus, the 2,3-dialkylated butadienes 6a-d are obtained by treating the diacetate 4 with two equivalents of the cuprates prepared fr

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