1-Acetonylpyridinium Chloride

≥99%

Reagent Code: #136293
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CAS Number 42508-60-1

science Other reagents with same CAS 42508-60-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 171.62 g/mol
Formula C₈H₁₀ClNO
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MDL Number MFCD00031949
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It serves as a pyridinium-based reagent in alkylation and acylation reactions, facilitating the introduction of acetonyl groups into target molecules. Its reactivity makes it valuable in the development of active ingredients in crop protection agents and in the synthesis of nitrogen-containing heterocyclic compounds. Also employed in research settings for modifying pyridine derivatives to enhance biological activity or solubility properties.

format_list_bulleted Product Specification

Test Parameter Specification
APPEARANCE White to Orange to Green powder to crystal
Purity (%) 99-100
Infrared Spectrum Conforms to Structure
Melting Point (C) 195.0-208.0
Solubility in H2O 0.1g/10ml, Clear

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿180.00
5g
10-20 days ฿880.00
25g
10-20 days ฿4,020.00
100g
10-20 days ฿16,020.00
1-Acetonylpyridinium Chloride
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It serves as a pyridinium-based reagent in alkylation and acylation reactions, facilitating the introduction of acetonyl groups into target molecules. Its reactivity makes it valuable in the development of active ingredients in crop protection agents and in the synthesis of nitrogen-containing heterocyclic compounds. Also employed in research settings for modifying pyridine derivatives to e

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It serves as a pyridinium-based reagent in alkylation and acylation reactions, facilitating the introduction of acetonyl groups into target molecules. Its reactivity makes it valuable in the development of active ingredients in crop protection agents and in the synthesis of nitrogen-containing heterocyclic compounds. Also employed in research settings for modifying pyridine derivatives to enhance biological activity or solubility properties.

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