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1,6-Dicyanododecafluorohexane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

3885-85-6

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3885-85-6 Usage

Physical state

Clear, colorless liquid

Solubility

Insoluble in water

Vapor pressure

Low at ambient temperatures

Uses

a. Polymerization agent
b. Solvent for various organic reactions
c. Surfactant
d. Lubricant in the electronics industry

Toxicity

Low toxicity

Environmental impact

Not known to cause significant adverse effects on human health or the environment

Safety precautions

Handle and store with care due to potential reactivity and flammability

Check Digit Verification of cas no

The CAS Registry Mumber 3885-85-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,8,8 and 5 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 3885-85:
(6*3)+(5*8)+(4*8)+(3*5)+(2*8)+(1*5)=126
126 % 10 = 6
So 3885-85-6 is a valid CAS Registry Number.

3885-85-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2,3,3,4,4,5,5,6,6,7,7-dodecafluorooctanedinitrile

1.2 Other means of identification

Product number -
Other names 1,6-DICYANODODECAFLUOROHEXANE

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:3885-85-6 SDS

3885-85-6Downstream Products

3885-85-6Relevant academic research and scientific papers

FLUORINATED IMIDOYLAMIDINES VULCANIZING AGENTS

-

Page/Page column 28, (2008/06/13)

The invention provides a compound and, tautomeric forms thereof having the formula (I): wherein Rf1 is selected from the group consisting of hydrogen, a straight chain, branched secondary or branched tertiary C1-C20 perfluoroalkyl group optionally containing ether or thioether linkages and C1-C10 perfluoroalicyclic group optionally containing ether or thioether groups; Rf2 is a straight or branched C1-C20 perfluoroalkylene group optionally substituted with ether and thiother linkages; and X is selected from the group consisting of fluorine and formula (II). . The invention also provides perfluoroelastomeric compositions cured with the perfluoroimidoylamidines of the invention as well as combinations of perfluoroimidoylamidines and other curing agents.

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