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Literature Sheets-Metal Catalysts,Ligands & Reagents for Organic Synthesis & other applications

Air-stable, Non-pyrophoric Phosphine Ligand Precursors PDF Document

Air-stable, Non-pyrophoric Phosphine Ligand Precursors Air-stable, Non-pyrophoric Phosphine Ligand Precursors

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Asymmetric Catalytic Allylic Substitution - Trost Ligands PDF Document

Asymmetric Catalytic Allylic Substitution - Trost Ligands Asymmetric Catalytic Allylic Substitution - Trost Ligands

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BASF Heterogeneous Catalysts and Applications Summary PDF Document

BASF Heterogeneous Catalysts and Applications Summary BASF Heterogeneous Catalysts and Applications Summary

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Boronate Esters and Boronic Acids PDF Document

Boronate Esters and Boronic Acids Boronate Esters and Boronic Acids for Suzuki Coupling

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Catalysts & Ligands for Ruthenium/Iridium Hydrogenation PDF Document

Catalysts & Ligands for Ruthenium/Iridium Hydrogenation These catalysts and ligands can be used in the hydrogenation of carbonyl functionalities or selected aromatic ketones.

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Chiral Phosphoric Acids PDF Document

Chiral Phosphoric Acids We offer over 100 Chiral Phosphoric Acids for R&D including: BINOL-, SPINOL-, and TADDOL derived CPA that can be applied as an effective tool for numerous en antioselective organic transformations.

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Chiral vicinal diamine ligands for asymmetric synthesis PDF Document

Chiral vicinal diamine ligands for asymmetric synthesis We offers a wide range of chiral vicinal diamines that are used as highly effective steering ligands for
transition-metal-catalyzed asymmetric reactions. These types of ligands are of great interest for the synthetic chemist who are working on active pharmaceutical ingredients, natural products, and agrochemicals.

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Dirhodium Catalysts PDF Document

Dirhodium Catalysts Rh2(R-PTAD)4, Rh2(S-PTAD)4, Rh2(R-BTPCP)4, Rh2(S-BTPCP)4, Rh2(R-DOSP)4, Rh2(S-DOSP)4

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Disulfide reducing agents for molecular diagnostics (THPP, TCEP) in gene chips PDF Document

Disulfide reducing agents for molecular diagnostics (THPP, TCEP) in gene chips Catalog # 15-6375
Tris(3-hydroxypropyl)phosphine, min. 84% THPP

Catalog # 15-7400
Tris(2-carboxyethyl)phosphine, hydrochloride, 99% TCEP

Disulfide reducing agents for molecular diagnostics

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DuPhos™ and BPE Technology PDF Document

DuPhos™ and BPE Technology DuPhos™ and BPE Technology for Asymmetric Catalytic Hydrogenation

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Enantiopure primary amine organocatalysts PDF Document

Enantiopure primary amine organocatalysts Enantiopure primary amine organocatalysts derived from cinchona alkaloids for iminium-enamime activation

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EvoluChem™ PhotoRedOx Products PDF Document

EvoluChem™ PhotoRedOx Products 98-7500 EvoluChem™ PhotoRedOx Box, 110V, Type A plug (USA electrical outlet)
98-7501 EvoluChem™ PhotoRedOx Box, 220V, Type C plug (EU electrical)
98-7550 EvoluChem™ PhotoRedOx Box (Temperature Controlled) 110V, Type A plug (USA electrical outlet)
98-7551 EvoluChem™ PhotoRedOx Box (Temperature Controlled) 220V, Type C plug )EU electrical outlet)
98-7600 EvoluChem™ PhotoRedOx Box Photochemistry Holder - 32 x 0.3ml vials
98-7650 EvoluChem™ PhotoRedOx Box Photochemistry Holder - 8 x 2ml vials
98-7790 EvoluChem™ PhotoRedOx Box Photochemistry Holder - 8 x 4ml vials
98-7700 EvoluChem™ PhotoRedOx Box Photochemistry Holder - 8 x 8ml vials
98-7780 EvoluChem™ PhotoRedOx Box Photochemistry Holder - 2 x 20 ml vials
98-7800 EvoluChem™ PhotoRedOx Box Light Source
98-7805 EvoluChem™ PhotoRedOx Box Light Source
98-7820 EvoluChem™ PhotoRedOx Box Light Source
98-7880 EvoluChem™ PhotoRedOx Box Light Source
98-7900 EvoluChem™ PhotoRedOx Box Light Source
98-7950 EvoluChem™ PhotoRedOx Box Light Source - Wavelength 450nm, Electric Power 18W, 110V, Type A plug (USA electrical outlet)
98-7955 EvoluChem PhotoRedOx Box Light Source - Wavelength 365nm, Electric Power 18W, 220V, Type C plug (EU electrical outlet)
98-7975 EvoluChem PhotoRedOx Box Light Source - Electric Power PAR20-18W, LG, Wavelength 380nm, 25 degrees, 110V, (USA electrical outlet)
98-7980 EvoluChem PhotoRedOx Box Light Source - Electric Power PAR20-18W, LG, Wavelength 380nm, 25 degrees, 220V, Type C plug (EU electrical outlet)
98-7820 EvoluChem PhotoRedOx Box Light Source - Wavelength 405nm, Electric Power 18W, 110V, (USA electrical outlet)
98-7880 EvoluChem PhotoRedOx Box Light Source - Wavelength 405nm, Electric Power 18W, 220V, Type C plug (EU electrical outlet)
98-7900 EvoluChem PhotoRedOx Box Light Source - Wavelength 425nm, Electric Power 18W, 110V, Type A plug (USA electrical outlet)
98-7905 EvoluChem PhotoRedOx Box Light Source - Wavelength 425nm, Electric Power 18W, 220V, Type C plug (EU electrical outlet)
98-7800 EvoluChem PhotoRedOx Box Light Source - Wavelength 450nm, Electric Power 18W, 110V (USA electrical outlet)
98-7805 EvoluChem PhotoRedOx Box Light Source - Wavelength 450nm, Electric Power 18W, 220V, Type C plug (EU electrical outlet)
98-7990 EvoluChem™ PhotoRedOx Box Light Source - Wavelength 525nm, Electric Power 18W, 110V, Type A plug (USA electrical outlet)
98-7991 EvoluChem™ PhotoRedOx Box Light Source - Wavelength 525nm, Electric Power 18W, 220V, Type C plug (EU electrical outlet)
98-8010 EvoluChem™ PhotoRedOx Box Light Source - Wavelength 650nm, Electric Power 18W, 110V, Type A plug (USA electrical outlet)
98-8011 EvoluChem™ PhotoRedOx Box Light Source - Wavelength 650nm, Electric Power 18W, 220V, Type C plug (EU electrical outlet)
96-7510 EvoluChem™ Photochemical Methylation Array Kit
96-7560 EvoluChem™ Photocatalytic Alkylation Kit
96-7520 EvoluChem™ Iridium/Nickel PhotoRedOx Base and Solvent Screening Kit 1
96-7530 EvoluChem™ Iridium/Nickel PhotoRedOx Base and Ligand Screening Kit 1
96-7540 EvoluChem™ Iridium/Nickel PhotoRedOx Base and Ligand Screening Kit 2
96-7550 EvoluChem™ Iridium/Nickel PhotoRedOx \ Base and Iridium Catalyst Screening Kit
96-7570 EvoluChem™ Iridium/Nickel PhotoRedOx Base and Solvent Screening Kit 2 (C-O coupling)
98-7850 EvoluChem™ Light proofing upgrade

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Fluorination and Trifluoromethylation - Selected Catalysts and Reagents PDF Document

Fluorination and Trifluoromethylation - Selected Catalysts and Reagents Fluorination and Trifluoromethylation - Selected Catalysts and Reagents
Trifluoromethylator®, PhenoFluor®Mix, SelectFluor™ and more...

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Gold AUROlite™ Nanoparticle Catalysts PDF Document

Gold AUROlite™ Nanoparticle Catalysts Strem Catalog #79-0160, 79-0165, 79-0170

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Hexammineruthenium(III) Chloride as an Electron Mediator for Rapid Whole Blood Glucose Detection PDF Document

Hexammineruthenium(III) Chloride as an Electron Mediator for Rapid Whole Blood Glucose Detection Hexammineruthenium(III) Chloride as an Electron Mediator for Rapid Whole Blood Glucose Detection Catalog #44-0620 CAS [14282-91-8]

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HiersoPHOS PDF Document

HiersoPHOS The “HiersoPHOS” family of ligands are ferrocenyl polyphosphine ligands which may be used in Palladium promoted catalytic transformations such as the functionalization of hetero-aromatic compounds and various carbon–carbon and carbon–nitrogen bond formation reactions (Suzuki-Miyaura coupling, Heck coupling, Buchwald-Hartwig cross-coupling as well as Sonogashira reactions).

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High Performance Carbon Supported Palladium Catalysts for Hydrogenation PDF Document

High Performance Carbon Supported Palladium Catalysts for Hydrogenation 46-1610, 46-1630 & 46-1660: Enhanced dispersion of these Pd particles on the high purity carbon support enables the catalysts' operation under mild conditions with higher selectivity and minimum unwanted side reactions. See the full sheet for more details on these products.

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High Purity Chiral Reagents PDF Document

High Purity Chiral Reagents High Purity Chiral Reagents

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High Quality Phosphorus Products PDF Document

High Quality Phosphorus Products Multi-kilo Samples from Strem ● Industrial Scale from Syensqo
97-0096, 97-0165, 97-0695, 97-0966, 97-1030, 97-1000, 97-1044, 97-1120, 97-1128, 97-1130, 97-1310, 97-1312, 97-1330, 97-1337, 97-1460, 97-1579, 97-1001, 97-5750, 97-5801, 97-6300, 97-6363, 97-1002, 97-6655, 97-6659, 97-6660, 97-6665, 97-7620, 97-7625, 97-7630, 97-1003

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Iridium Catalysts PDF Document

Iridium Catalysts for Hydrogen Isotope Exchange and Catalytic Hydrogenation Processes

Item #'s - 77-1810, 77-1825, 77-1830, 77-1840, 77-1845 & 77-1850

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Metathesis Catalysts Developed by XiMo PDF Document

Metathesis Catalysts Developed by XiMo Molybdenum Metathesis Catalysts Developed by XiMo. Includes: 42-0510, 42-0515, 42-0520, 42-0525, 42-0530, 42-0535, 42-0540, 42-0545, 42-0550, 42-0555, 42-0560, 42-0565 and 42-0575. Also includes Triethylaluminum paraffin pellets, 13-1905

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Metathesis Catalysts and Ligands (Molybdenum-based Schrock Catalysts) PDF Document

Metathesis Catalysts and Ligands (Molybdenum-based Schrock Catalysts) Molybdenum-based Schrock Catalysts, BIPHEN ligands and other ligands used for metathesis.

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Milstein Catalysts PDF Document

Milstein Catalysts Milstein Catalysts - 44-0081, 44-0091, 44-0525

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NHC Nickel Catalyst PDF Document

NHC Nickel Catalyst NHC Nickel Catalyst for amination of aryl chlorides and reductive couplings
Item#': 28-1040

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Polyisobutyl (PIB) Ligands for Separable Homogeneous Catalysts PDF Document

Polyisobutyl (PIB) Ligands for Separable Homogeneous Catalysts Phase-selectively soluble polyisobutyl-bound ligands developed by Professor David Bergbreiter’s group can be used to prepare versions of homogeneous transitional metal complexes and organocatalysts that can be recovered and recycled.

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Rare-Earth BINOLate Compounds PDF Document

Rare-Earth BINOLate Compounds Rare earth metal Binolate complexes serve as bench stable precatalysts for Shibasaki's REMB catalysts. These compounds give improved levels of stereoselectivity in reactions such as MIchael additions, aza- Michael additions and direct Aldol reactions.
Product #'s : 57-0250, 59-1000, 70-0130 & 39-5850

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Rh2(DOSP)4 and Rh2(PTAD)4 PDF Document

Rh2(DOSP)4 and Rh2(PTAD)4 Rh2(DOSP)4 and Rh2(PTAD)4 for C-H Activation by means of Metal-Carbenoid-Induced C-H Insertion

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Selected Ruthenium Metathesis Catalysts PDF Document

Selected Ruthenium Metathesis Catalysts Selected Ruthenium Metathesis Catalysts

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SaBOX Ligands PDF Document

SaBOX Ligands SaBOX Ligands

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Silica Scavengers PDF Document

Silica Scavengers Enhanced cost effective performance through a new Scavenger design with:
• Multiple mono and polydentate Functional Groups each with very high Affinity for the Target;
• Functional Groups present in numerous different spatial arrangements and in specific combination with other Functional Groups results in
numerous different binding modes to the Target;
• Strong binding modes designed for each of the different Target species present.

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Sodium tetraethylborate as a Derivatizing Agent PDF Document

Sodium tetraethylborate as a Derivatizing Agent Sodium tetraethylborate as a Derivatizing Agent for the Detection of Organotin, -lead, and –mercury - Catalog # 11-0575 [15523-24-7]

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Takasago BRIDP Ligands PDF Document

Takasago BRIDP Ligands Takasago BRIDP Ligands

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TUC Ligands PDF Document

TUC Ligands TUC Ligands for Michael additions and hydrazination

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