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114136-87-7

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114136-87-7 Usage

General Description

N,N'-Bis(2-methyl-2-nitropropyl)hexamethylenediamine is a chemical compound with the molecular formula C14H30N4O4. It is a diamine compound, containing two amino groups and two nitro groups. It is commonly used as a curing agent for epoxy resins, providing increased flexibility and impact resistance to the cured resin. It is also used as a stabilizer for polymers and as an intermediate in the synthesis of other organic compounds. This chemical is classified as hazardous, with potential health hazards including skin and eye irritation, and respiratory sensitization. It is important to handle and use this chemical with care, following proper safety protocols to minimize the risk of adverse effects on human health and the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 114136-87-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,1,3 and 6 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 114136-87:
(8*1)+(7*1)+(6*4)+(5*1)+(4*3)+(3*6)+(2*8)+(1*7)=97
97 % 10 = 7
So 114136-87-7 is a valid CAS Registry Number.

114136-87-7SDS

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 N,N'-bis(2-methyl-2-nitropropyl)hexane-1,6-diamine

1.2 Other means of identification

Product number -
Other names 1,6-Hexanediamine,N,N'-bis(2-methyl-2-nitropropyl)

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:114136-87-7 SDS

114136-87-7Synthetic route

N,N'-bis(2-methyl-2-nitropropyl)-1,6-hexanediamine
114136-87-7

N,N'-bis(2-methyl-2-nitropropyl)-1,6-hexanediamine

N,N'-(hexane-1,6-diyl)bis(2-methylpropane-1,2-diamine)
1287302-78-6

N,N'-(hexane-1,6-diyl)bis(2-methylpropane-1,2-diamine)

Conditions
ConditionsYield
With hydrogen; RaNi 3111 In methanol; water at 65℃; under 26101 Torr; for 1h;97%
acetic anhydride
108-24-7

acetic anhydride

N,N'-bis(2-methyl-2-nitropropyl)-1,6-hexanediamine
114136-87-7

N,N'-bis(2-methyl-2-nitropropyl)-1,6-hexanediamine

N,N'-diacetyl-N,N'-bis(2-methyl-2-nitropropyl)-1,6-hexanediamine

N,N'-diacetyl-N,N'-bis(2-methyl-2-nitropropyl)-1,6-hexanediamine

Conditions
ConditionsYield
In benzene for 2h; Ambient temperature;76%
1,6-Hexanediamine
124-09-4

1,6-Hexanediamine

formaldehyd
50-00-0

formaldehyd

hexane
110-54-3

hexane

2-nitropropane
79-46-9

2-nitropropane

N,N'-bis(2-methyl-2-nitropropyl)-1,6-hexanediamine
114136-87-7

N,N'-bis(2-methyl-2-nitropropyl)-1,6-hexanediamine

N,N-bis(2-methyl-2-nitropropyl)-1,6-diaminohexane

N,N-bis(2-methyl-2-nitropropyl)-1,6-diaminohexane

Conditions
ConditionsYield
In methanol; water; toluene

114136-87-7Upstream product

114136-87-7Downstream Products

114136-87-7Relevant articles and documents

Rubber composition

-

, (2008/06/13)

Dynamic properties of valcanized rubber are improved, without accelerating scorching property remark-ably nor deteriorating flex-cracking resistance, by incorporating in a filler-containing natural or synthetic rubber composition, a dinitrodiamine derivative repre-sented by the general formula wherein A represents a divalent aliphatic group, a divalent cycloaliphatic group, a divalent aromatic group or a group represented by the formula -CH2-X-CH2-, wherein X represents a cycloalkylene group or a phenylene group, provided that if A represents a cycloaliphatic group or an aromatic group, the two carbon atoms in A which are bonding to the nitrogen atom are not vicinal to each other; R and R′ independently represent hydrogen atom or an alkyl group having 1 - 12 carbon atoms and may conjointly form a ring; and R″ represents hydrogen atom, an aliphatic group, a cycloaliphatic group or an aromatic group. A process for producing the dinitrodiamine derivatives is also disclosed.

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