(N-Methyl-N-phenylamino)triphenylphosphonium Iodide

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Reagent Code: #217644
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CAS Number 34257-63-1

science Other reagents with same CAS 34257-63-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 495.34 g/mol
Formula C₂₅H₂₃INP
badge Registry Numbers
MDL Number MFCD00040544
inventory_2 Storage & Handling
Storage Room temperature, dryness, inert gas storage

description Product Description

Used as a photoacid generator in photopolymerization processes, particularly in advanced lithography for semiconductor manufacturing. Upon exposure to light, it releases acid that initiates polymerization or cross-linking in resist materials, enabling high-resolution patterning. Also employed in organic synthesis as a phosphonium-based reagent for Wittig-type reactions, facilitating carbon-carbon bond formation. Its thermal stability and solubility in organic solvents make it suitable for thin-film applications and optoelectronic device fabrication.

Available Sizes & Pricing

Size Availability Unit Price Quantity
50mg
10-20 days ฿310.00
250mg
10-20 days ฿760.00
1g
10-20 days ฿2,550.00
(N-Methyl-N-phenylamino)triphenylphosphonium Iodide
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Used as a photoacid generator in photopolymerization processes, particularly in advanced lithography for semiconductor manufacturing. Upon exposure to light, it releases acid that initiates polymerization or cross-linking in resist materials, enabling high-resolution patterning. Also employed in organic synthesis as a phosphonium-based reagent for Wittig-type reactions, facilitating carbon-carbon bond formation. Its thermal stability and solubility in organic solvents make it suitable for thin-film appli

Used as a photoacid generator in photopolymerization processes, particularly in advanced lithography for semiconductor manufacturing. Upon exposure to light, it releases acid that initiates polymerization or cross-linking in resist materials, enabling high-resolution patterning. Also employed in organic synthesis as a phosphonium-based reagent for Wittig-type reactions, facilitating carbon-carbon bond formation. Its thermal stability and solubility in organic solvents make it suitable for thin-film applications and optoelectronic device fabrication.

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