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4-(dimethylamino)-1-methylpyridinium iodide, also known as 4-DMAPy, is a cationic organic compound with the chemical formula C8H12N+I-. It is a derivative of pyridinium, featuring a dimethylamino group at the 4-position and a methyl group at the 1-position. 4-(dimethylamino)-1-methylpyridinium iodide is often used as a precursor in the synthesis of various organic compounds and as a reagent in chemical reactions. It is soluble in water and polar organic solvents, and its ionic nature allows it to participate in various electrophilic reactions. 4-DMAPy is also known for its potential applications in the field of materials science, particularly in the development of conductive polymers and as a dopant in organic electronics.

7538-79-6

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7538-79-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7538-79-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,3 and 8 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7538-79:
(6*7)+(5*5)+(4*3)+(3*8)+(2*7)+(1*9)=126
126 % 10 = 6
So 7538-79-6 is a valid CAS Registry Number.

7538-79-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N,1-trimethylpyridin-1-ium-4-amine,iodide

1.2 Other means of identification

Product number -
Other names Pan-W-24

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:7538-79-6 SDS

7538-79-6Downstream Products

7538-79-6Relevant academic research and scientific papers

Base-Free Generation of Organic Electron Donors from Air-Stable Precursors

Tintori, Guillaume,Nabokoff, Pierre,Buhaibeh, Ruqaya,Bergé-Lefranc, David,Redon, Sébastien,Broggi, Julie,Vanelle, Patrice

, p. 3148 - 3153 (2018/03/13)

Organic electron donors (OEDs) are powerful reducing agents recognized for their potential in the reduction of challenging substrates and in original applications. Nonetheless, their low stability in atmospheric oxygen or over time complicates their manipulation and storage. To overcome these constraints and enhance OED practicality, new air- and moisture-stable aminopyridinium carboxylate and carbonate precursors were synthesized and thermally activated to generate the potent electron donor in situ. Carboxylate adducts proved to be excellent latent OED systems, enabling the facile and efficient reduction of challenging substrates. Their reduction properties were correlated to their structural characteristics by thermogravimetric and spectroscopic analysis.

Efficient macrocyclization achieved via conformational control using intermolecular noncovalent π-cation/arene interactions

Bolduc, Philippe,Jacques, Alexandre,Collins, Shawn K.

supporting information; experimental part, p. 12790 - 12791 (2010/11/04)

Quinolinium salt 3 is an effective additive that acts as a conformation control element (CCE) to promote macrocyclization to form rigid cyclophanes via olefin metathesis or Glaser-Hay coupling, which do not cyclize in the absence of the additive. The additives are easily synthesized and highly modifiable and have solubility profiles which allow for simple recovery via filtration.

Preparation and in vitro evaluation of monoquaternary inhibitors of brain cholinesterases

Jun, Daniel,Paar, Martin,Binder, Jiri,Marek, Jan,Pohanka, Miroslav,Stodulka, Petr,Kuca, Kamil

scheme or table, p. 500 - 503 (2010/04/23)

Acetylcholinesterase inhibitors are currently of high interest due to the many reasons. Among them, Alzheimer's disease drugs are of great interest. In this study, eleven monoquaternary pyridinium salts substituted by different groups (electron donors and

Polycations-12. The synthesis of liquid ionic phosphates (lips) from mono- and polycationic ammonium halides

Lall, Sharon,Behaj, Valbona,Mancheno, Danny,Casiano, Robert,Thomas, Marie,Rikin, Amir,Gaillard, Jennifer,Raju, Ravinder,Scumpia, Alexander,Castro, Steve,Engel, Robert,Cohen, JaimeLee Iolani

, p. 1530 - 1540 (2007/10/03)

Preparations are reported for an extensive series of phosphate salts of polyammonium species from the corresponding halide salts. The phosphate salts, as anhydrous materials, are liquid at or near room temperature. Three approaches for the preparation of these materials are noted, including treatment with aqueous hexafluorophosphoric acid, classical ion exchange methods, and treatment with 85% phosphoric acid. The last of these provides the most desirable results. Several monocationic phosphate salts have also been prepared for comparison with other types of ionic liquids.

Second-order hyperpolarizability of pyridinium cations

Anwar,Duan, Xuan-Ming,Komatsu, Kyoji,Okada, Shuji,Matsuda, Hiro,Oikawa, Hidetoshi,Nakanishi, Hachiro

, p. 247 - 248 (2007/10/03)

The second-order hyperpolarizability (β) of pyridinium cations with cutoff (λco) shorter than 400 nm were studied by semiempirical calculation and the hyper-Rayleigh scattering (HRS) technique. The β value of 4-dimethylaminopyridinium (λco= 390 nm) was evaluated to be about 1.5 times larger than that of p-nitroaniline (λco= 473 nm) in methanolic solution using 1064 nm light as a fundamental beam.

Menschutkin Reactions of Bicyclic Aliphatic Amines and of Pyridine Derivatives with Methyl Iodide. Extended Broensted Treatments and Isokinetic Relationships in Acetonitrile-Methanol

Kondo, Yasuhiko,Uematsu, Ryoichi,Nakamura, Yoshinobu,Kusabayashi, Shigekazu

, p. 1219 - 1224 (2007/10/02)

The rate constants, activation parameters for the Menschutkin reactions for five bases with methyl iodide, and the enthalpies of solution for the relevant species of the reactions have been determined in acetonitrile-methanol.The bases are quinuclidine, 1,4-diazabicyclooctane, and 4-cyano-, 4-t-butyl-, and 4-dimethylamino-pyridine.The coefficients of empirical energy correlations defined in terms of 'more physical' energies, extended Broensted treatments, αphys' and isokinetic temperatures, βphys' have been determined for these reactions.Discussion is provided on the physical meaning of these coefficients in relation to the characteristics of the activated complex.

Empirical Analysis on the Constituent Terms of Transfer Enthalpies. Quarternary Ammonium Ions in Acetonitrile-Methanol Mixtures.

Kondo, Yasuhiko,Uematsu, Ryoichi,Nakamura, Yoshinobu,Kusabayashi, Shigekazu

, p. 111 - 116 (2007/10/02)

Through an empirical analysis of transfer enthalpies in acetonitrile-methanol mixtures using ten quaternary ammonium ions, an equation which expresses the behaviour of the transfer enthalpy as a function of solvent composition has been derived: .On the basis of this equation it is suggested that the transfer enthalpy includes at least three types of interaction, a protophobic interaction, an electrostatic interaction and another interaction, presumably a specific interaction such as dipole-dipole or acid-base association.

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