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79848-85-4

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79848-85-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79848-85-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,8,4 and 8 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 79848-85:
(7*7)+(6*9)+(5*8)+(4*4)+(3*8)+(2*8)+(1*5)=204
204 % 10 = 4
So 79848-85-4 is a valid CAS Registry Number.

79848-85-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-imino-1,3,3-trimethylcyclohexane-1-carbonitrile

1.2 Other means of identification

Product number -
Other names 3-cyano-3,5,5-trimethylcyclohexaneimine

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:79848-85-4 SDS

79848-85-4Relevant articles and documents

Method for preparing IPDI (isophorone diisocyanate)

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, (2019/06/13)

The invention discloses a method for preparing IPDI (isophorone diisocyanate). The method comprises the following steps: (1) isophorone and hydrogen cyanide are subjected to a reaction in the presenceof a catalyst to obtain isophorone nitrile; (2) isophorone nitrile obtained in step (1), ammonia and hydrogen are subjected to a reaction in the presence of a catalyst to obtain isophorone diamine; (3) isophorone diamine is subjected to a phosgenation reaction to obtain IPDI, wherein the content of impurities containing secondary amine groups in isophorone diamine subjected to the phosgenation reaction in step (3) is smaller than or equal to 0.5wt%, preferably smaller than or equal to 0.3wt%, and more preferably smaller than or equal to 0.1wt%. By means of the method, content of hydrolyzed chlorine in the IPDI product can be effectively reduced, the yellowing resistance of the product is effectively improved, and the harm that downstream products are unqualified due to existence of hydrolyzed chlorine in the product is reduced.

3-aminomethyl -3, 5, 5-trimethyl method for preparing cyclohexylamine (by machine translation)

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Paragraph 0061-0065, (2017/03/14)

The present invention provides a 3-aminomethyl -3, 5, 5-trimethyl method for preparing cyclohexylamine. 3-cyano -3, 5, 5-trimethyl cyclohexyl imine the inferior amination reaction material, in the subsequent steps, with the assistance of the circulating material in the 1st 1st-stage hydrogenation reaction by the hydrogenation reaction material, and can effectively inhibit the generation of HCN product, then in the heating can decompose under the action of the alkaline additive to 2nd stage hydrogenation reaction, then heating the alkaline additive decomposition, decomposition reaction material as circulation material part of a 1st-stage hydrogenation reaction to return as adjuvant, 3rd levels of the remaining part of the hydrogenation reaction, to obtain 3-aminomethyl -3, 5, 5-trimethyl cyclohexane, in the product can be effectively reduced 3-cyano -3, 5, 5-trimethyl cyclohexane and secondary amines the content of the product. (by machine translation)

METHOD FOR PREPARING 3-AMINOMETHYL-3,5,5-TRIMETHYL CYCLOHEXYLAMINE

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Paragraph 0058-0063; 0071-0074, (2016/12/22)

The present invention provides a method for preparing 3-aminomethyl-3,5,5-trimethyl cyclohexylamine. The method comprises: a) reacting 3-cyano-3,5,5-trimethyl cyclohexanone with excess primary amine as well as removing the water generated from the reaction, so that IPN is substantially converted into imine compounds; b) in the presence of an ammonolysis catalyst, mixing the product of step a) with liquid ammonia, making the imine compound perform ammonolysis reaction to generate 3-cyano-3,5,5-trimethyl cyclohexylimine and the primary amine; and c) in the presence of hydrogen and a hydrogenation catalyst, hydrogenating 3-cyano-3,5,5-trimethyl cyclohexylimine obtained in step b) to obtain 3-aminomethyl-3,5,5-trimethyl cyclohexylamine. The method of the present invention avoids the generation of 3,5,5-trimethyl cyclohexanol and 3-aminomethyl-3,5,5-trimethyl cyclohexanol as the major by-products in the prior art, thereby improving the yield of 3-aminomethyl-3,5,5-trimethyl cyclohexylamine.

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