Skip to Content
Merck
All Photos(1)

Documents

Z744078

Sigma-Aldrich

395 nm Light source

Synonym(s):

395nm LED Light Module

Sign Into View Organizational & Contract Pricing


About This Item

UNSPSC Code:
39101616
NACRES:
NC.25

Related Categories

General description

The 395nm LED Light Module is used with the Penn PhD Photoreactor M2 for chemists and researchers to accelerate chemical reactions using photoredox catalysis.

Features and Benefits

Features and Benefits of Penn PhD Photoreactor M2
  • Modular design allows for use with a variety of wavelengths 365nm – 450nm
  • 360 degree reflective environment maximizes surface area photon capture
  • Light shield interlock prevents user exposure to harmful light rays
  • Interactive touch screen controls reaction parameters
  • Intertek ETL, CE, and CB approved
  • User defined parameters including temperature, light intensity, fan speed and stirring
  • Auto stop, pause and reset options
  • Supports vial sizes gc, 4, 8, 20, 40 ml
  • Temp feedback using a k-type thermocouple

related product

Product No.
Description
Pricing

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Articles

The application of radical chemistry towards organic synthesis is well-developed and wide-reaching, though often hampered by a dependence on toxic radical initiators.

Learn about the applications of chiral oxazaborolidinium ions (COBIs) as Lewis acid catalysts in different asymmetric reactions such as cyclopropanation, epoxidation, and radical reactions along with details of their catalytic action.

This article details the latest progress in synthesizing alkylsulfonyl fluorides through different approaches that utilize photoredox catalysis, electrocatalysis, transition-metal catalysis, and organocatalysis. The alkylsulfonyl fluorides thus prepared could be utilized further in sulfur(VI) fluoride exchange (SuFEx) click reactions.

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service