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2301-80-6

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2301-80-6 Usage

Description

1,4-DIMETHYLPYRIDINIUM IODIDE 99 is a quaternary ammonium salt with a molecular formula of C7H10IN and a molecular weight of 263.07 g/mol. It is a white to off-white crystalline solid that is soluble in water. The "99" in its name signifies its high purity level of 99%. This chemical compound is commonly used as a reagent in organic synthesis and is known for its versatile applications in chemical synthesis.

Uses

Used in Organic Synthesis:
1,4-DIMETHYLPYRIDINIUM IODIDE 99 is used as a reagent for various organic reactions, facilitating the synthesis of complex organic molecules and contributing to the development of new chemical compounds.
Used as a Phase-Transfer Catalyst:
In the field of organic chemistry, 1,4-DIMETHYLPYRIDINIUM IODIDE 99 is utilized as a phase-transfer catalyst to enhance the efficiency of reactions involving both organic and inorganic components. This application is particularly beneficial in promoting reactions that would otherwise be slow or inefficient due to differences in solubility between the reactants.
Used in Pharmaceutical Synthesis:
1,4-DIMETHYLPYRIDINIUM IODIDE 99 plays a crucial role in the synthesis of pharmaceuticals and other fine chemicals. Its ability to act as a catalyst and reagent in various chemical reactions makes it a valuable component in the production of medications and other specialty chemicals.
Used in Laboratory and Industrial Settings:
Due to its high purity and versatile applications, 1,4-DIMETHYLPYRIDINIUM IODIDE 99 is commonly used in both laboratory and industrial settings. Its solubility in water and effectiveness in a wide range of chemical reactions make it a preferred choice for researchers and manufacturers alike.

Check Digit Verification of cas no

The CAS Registry Mumber 2301-80-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,0 and 1 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2301-80:
(6*2)+(5*3)+(4*0)+(3*1)+(2*8)+(1*0)=46
46 % 10 = 6
So 2301-80-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H10N/c1-7-3-5-8(2)6-4-7/h3-6H,1-2H3/q+1

2301-80-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4-Dimethylpyridinium iodide

1.2 Other means of identification

Product number -
Other names 1,4-DIMETHYLPYRIDINIUM IODIDE

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:2301-80-6 SDS

2301-80-6Relevant articles and documents

Competing processes in the photochemistry of picolines and their N-methyl salts: photoinduced charge transfer, phototransposition and photohydration

Bla?ek Bregovi?, Vesna,Basari?, Nikola

, p. 859 - 871 (2017/02/10)

Photochemical reactivity of a series of picolines and their N-methylated salts has been investigated by preparative irradiations and UV–vis spectroscopy. Understanding competing photochemical processes and knowledge of their relative efficiencies is important in the application of pyridines as photocages or in the synthesis of complex polycycles. Contrary to previous reports for the gas phase, picolines are not reactive in the phototransposition, presumably due to protonation of the pyridine nitrogen in the excited state. Deuterium exchange was observed upon irradiation in CD3CN–D2O, but it was rationalized by photoionization and radical formation. On the other hand, N-methylated picoline salts are not protonated upon excitation. They undergo photohydration and phototransposition (ΦR?=?0.01–0.06). Upon irradiation of iodides, azabicyclic [3.1.0] hydration products were obtained. A difference in product distribution was observed between iodides and perchlorates, due to photoelimination of perchloric acid leading to the thermal aziridine ring opening. Moreover, excitation of iodide derivatives gives rise to change transfer transition forming iodide radicals that eventually give I3 ? with the quantum efficiency ΦR?=?0.015–0.02.

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