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N,N-dicyclohexylcyclohexanamine is an organic compound with the chemical formula C18H33N. It is a white crystalline solid that is soluble in organic solvents and has a molecular weight of 263.46 g/mol. N,N-dicyclohexylcyclohexanamine is primarily used as a curing agent for epoxy resins, enhancing their mechanical properties, thermal stability, and chemical resistance. It is also employed as a cross-linking agent in various polymer systems, contributing to improved adhesion and durability. Due to its chemical structure, N,N-dicyclohexylcyclohexanamine exhibits low volatility and minimal toxicity, making it a preferred choice in industrial applications where safety and performance are crucial.

7335-09-3

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7335-09-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7335-09-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,3 and 5 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7335-09:
(6*7)+(5*3)+(4*3)+(3*5)+(2*0)+(1*9)=93
93 % 10 = 3
So 7335-09-3 is a valid CAS Registry Number.
InChI:InChI=1/C18H33N/c1-4-10-16(11-5-1)19(17-12-6-2-7-13-17)18-14-8-3-9-15-18/h16-18H,1-15H2

7335-09-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N-dicyclohexylcyclohexanamine

1.2 Other means of identification

Product number -
Other names tricyclohexyl-amine

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:7335-09-3 SDS

7335-09-3Relevant academic research and scientific papers

Formation of secondary or tertiary aliphatic amines in aqueous media

Marieta Simion, Alina,Arimura, Takashi,Miyazawa, Akira,Simion, Cristian,Surya Prakash,Olah, George A.,Tashiro, Masashi

scheme or table, p. 2859 - 2865 (2009/12/03)

Secondary and tertiary amines can be easily obtained from primary and secondary amines, respectively, in completely aqueous media, in the presence of a bicatalytic system formed of cheap commercial aluminum (Al) powder and 5% rhodium (Rh) or ruthenium (Ru) deposed on charcoal.

Reductive amination with 5-ethyl-2-methylpyridine borane

Burkhardt, Elizabeth R.,Coleridge, Brian M.

, p. 5152 - 5155 (2008/12/20)

We report a new amine borane, 5-ethyl-2-methylpyridine borane complex (PEMB) useful for reductive aminations of ketones and aldehydes in methanol or neat. Two of the three hydrides on PEMB are effectively utilized maximizing the economy of the reagent.

Cyclization of α,ω Aliphatic Diamines and Conversion of Primary Amines to Symmetrical Tertiary Amines by a Homogeneous Ruthenium Catalyst

Bui-The-Khai,Concilio, Carlo,Porzi, Gianni

, p. 1759 - 1760 (2007/10/02)

α,ω Aliphatic diamines were cyclized to heterocyclic amines by being heated at 180 deg C for 5 h with RuCl2(Ph3P)3 in diphenyl ether.Primary amines having an α-hydrogen atom are converted to symmetrical tertiary amines by being heated at 185 or 235 deg C for 8 h with RuCl3*3H2O and Ph3P in THF solution.

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