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49840-61-1

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49840-61-1 Usage

Explanation

Different sources of media describe the Explanation of 49840-61-1 differently. You can refer to the following data:
1. The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 10 carbon (C) atoms, 24 hydrogen (H) atoms, and 4 nitrogen (N) atoms.
2. TMTCH is a short form or common name for 1,4-Piperazinediamine, N,N,N,N-tetramethyl-(9CI), which is used for convenience and easier communication.
3. The compound belongs to the class of piperazine derivatives, which are chemical compounds derived from piperazine, a heterocyclic amine.
4. 1,4-Piperazinediamine, N,N,N,N-tetramethyl-(9CI) is used as a curing agent in the production of epoxy resins, which are thermosetting polymers. It helps in the hardening process, resulting in durable and strong materials.
5. The compound is also used as a stabilizer in the production of polymers, which are large molecules composed of repeating structural units. It helps maintain the stability and quality of the polymers during their synthesis.
6. In the petroleum industry, 1,4-Piperazinediamine, N,N,N,N-tetramethyl-(9CI) is used as a corrosion inhibitor. It helps prevent the corrosion of metal surfaces, which is crucial for maintaining the integrity of pipelines and storage tanks.
7. At room temperature, the compound exists as a white crystalline solid, which means it has a well-defined structure and appearance.
8. Due to potential health hazards associated with its use, the compound's application is regulated. This is to ensure that exposure to humans and the environment is minimized and controlled.
9. The compound's use is also regulated because of its potential environmental impact. This helps to prevent contamination and protect ecosystems from harm.

Chemical Class

Piperazine derivative

Use as a curing agent

Epoxy resins

Use as a stabilizer

Polymer production

Use as a corrosion inhibitor

Petroleum industry

Physical State

White crystalline solid

Health Hazards

Regulated use

Environmental Impact

Regulated use

Check Digit Verification of cas no

The CAS Registry Mumber 49840-61-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,9,8,4 and 0 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 49840-61:
(7*4)+(6*9)+(5*8)+(4*4)+(3*0)+(2*6)+(1*1)=151
151 % 10 = 1
So 49840-61-1 is a valid CAS Registry Number.

49840-61-1SDS

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 1-N,1-N,4-N,4-N-tetramethylpiperazine-1,4-diamine

1.2 Other means of identification

Product number -
Other names tetra-N-methyl-piperazine-1,4-diamine

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:49840-61-1 SDS

49840-61-1Upstream product

49840-61-1Downstream Products

49840-61-1Relevant articles and documents

Oxidation of Molecules Containing Two Tetraalkylhydrazine Units

Nelsen, Stephen F.,Willi, Mark R.

, p. 2081 - 2089 (2007/10/02)

Cyclic voltammetry studies have been carried out on several bishydrazines.Me2NNMe(CH2)nNMeNMe2, n = 2-4 (2-4), and 1,4-bis(dimethylamino)piperazine (11) have only a small separation between their first and second oxidation potentials and give dications which are short-lived in solution (lifetimes below a few milliseconds).In contrast, pentacyclic bishydrazine 14 and tetracyclic bishydrazines 16 and 17 have formal potentials that differ by 0.29, 0.21, and 0.19 V, respectively, and give dications which are long-lived in solution (their lifetimes exceed seconds).Hexacyclic bishydrazines 12 and 13 have a much larger separation in formal pot entials for oxidation and give short-lived dications.The shapes of the tetracyclic and pentacyclic compounds are discussed, as is the implication of these results for the consideration of a hydrazine radical cation interacting with a neutral hydrazine.

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