Merck
CN
All Photos(6)

Documents

Z744035

Sigma-Aldrich

Penn PhD Photoreactor M2

Sign Into View Organizational & Contract Pricing

Synonym(s):
photoreactor

AC/DC input

100 - 240 V AC, 50/60 Hz

feature

thermocouple type K-Type Thermocouple
(Touch Screen: 3.5” TFT LCD; 320 x 480 resolution)

reaction suitability

reaction type: Photocatalysis
reagent type: catalyst

parameter

(Variable stir bar control 100 - 2000 RPM)
0-95% RH at 10-40 °C

W × H × D

11.4 cm × 27.2 cm × 27.9 cm
4.5 in. × 10.7 in. × 11.0 in.

General description

The Penn PhD Photoreactor M2 is a benchtop instrument designed for chemists and researchers to accelerate chemical reactions using photoredox catalysis. The Photoreactor M2 combines LED illumination, mechanical stirring and cooling into one device. The user defined parameters of temperature, intensity, stir rate and time, create a valuable tool for repeatability, traceability, efficiency and consistency of results. The Photoreactor M2 addresses the potential to streamline synthetic sequences, and create valuable strategies for addressing some of the challenges of molecule construction in drug discovery.

Features and Benefits

  • Modular design allows for use with a variety of wavelengths: 450 nm (included), 420 nm (sold separately), 395 nm (sold separately) and 365 nm (sold separately)
  • 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
  • Multi-vial holders are available to allow four 8 mL vials and five 4 mL vials reactions to be run in parallel.
  • Temp feedback using a k-type thermocouple
Regional Plug Types Available
  • Z744035-1EA-US: type B
  • Z744035-1EA- IN: type D
  • Z744035-1EA-EU-E: type E
  • Z744035-1EA-EU-F: type F
  • Z744035-1EA-UK: type G
  • Z744035-1EA-CN: type I
  • Z744035-1EA-CH: type J

Photocatalysis Technology Spotlight

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?

Documents related to the products that you have purchased in the past have been gathered in the Document Library for your convenience.

Visit the Document Library

Difficulty Finding Your Product Or Lot/Batch Number?

Product numbers are combined with Pack Sizes/Quantity when displayed on the website (example: T1503-25G). Please make sure you enter ONLY the product number in the Product Number field (example: T1503).

Example:

T1503
Product Number
-
25G
Pack Size/Quantity

Additional examples:

705578-5MG-PW

PL860-CGA/SHF-1EA

MMYOMAG-74K-13

1000309185

enter as 1.000309185)

Having trouble? Feel free to contact Technical Service for assistance.

Lot and Batch Numbers can be found on a product's label following the words 'Lot' or 'Batch'.

Aldrich Products

  • For a lot number such as TO09019TO, enter it as 09019TO (without the first two letters 'TO').

  • For a lot number with a filling-code such as 05427ES-021, enter it as 05427ES (without the filling-code '-021').

  • For a lot number with a filling-code such as STBB0728K9, enter it as STBB0728 without the filling-code 'K9'.

Not Finding What You Are Looking For?

In some cases, a COA may not be available online. If your search was unable to find the COA you can request one.

Request COA

Articles

Photoredox catalysis is a powerful synthetic methodology to form challenging covalent bonds using light irradiation. It is effective for light-driven polymer and small molecule synthesis.

Csp2- and Csp-hybridized coupling reactions are established catalytic approaches. However, multi-step Csp3- and Csp2-coupling reactions of boronic acids and related derivatives are still limited by ineffective two-electron transmetalation reactions.

While Markovnikov alkene reactivity is very well developed and utilized commonly in the synthesis of commodity and research chemicals, catalytic access to the anti-Markovnikov-selective adducts is a much less-developed endeavor.

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