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2-Butene-1,4-diaminium, N1,N1,N1,N4,N4,N4-hexamethyl-, chloride (1:2) is a complex organic compound with the chemical formula C8H20N2.2Cl. It is a derivative of 2-butene-1,4-diamine, where the two nitrogen atoms are each bonded to three methyl groups, resulting in a hexamethyl-substituted diammonium structure. 2-Butene-1,4-diaminium,N1,N1,N1,N4,N4,N4-hexamethyl-, chloride (1:2) is known for its ability to form salts with chloride ions, and it is often used in chemical research and industrial applications due to its unique properties. The 1:2 ratio in the name indicates that one molecule of the diammonium compound reacts with two chloride ions, forming a salt with a specific stoichiometry.

7596-31-8

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7596-31-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7596-31-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,9 and 6 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 7596-31:
(6*7)+(5*5)+(4*9)+(3*6)+(2*3)+(1*1)=128
128 % 10 = 8
So 7596-31-8 is a valid CAS Registry Number.

7596-31-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name trimethyl-[(E)-4-(trimethylazaniumyl)but-2-enyl]azanium,hydrochloride

1.2 Other means of identification

Product number -
Other names -

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

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More Details:7596-31-8 SDS

7596-31-8Downstream Products

7596-31-8Relevant academic research and scientific papers

Properties of onium salts of phosphorus and nitrogen

Ovakimyan,Barsegyan,Kikoyan,Indzhikyan

, p. 1074 - 1076 (2005)

Ammonium and phosphonium halides when heated with excess dimethyl or diethyl phosphite can undergo anion exchange as a result of alkylation of halide ions with dialkyl phosphites. Experimental data were obtained, that cast some doubt in the commonly accepted opinion that reactions of tertiary amines and phosphines with dihalides in apolar media result in exclusive formation of monosalts. 2005 Pleiades Publishing, Inc.

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