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C–H Activation Catalysts

Metal-catalyzed C–H functionalization is an effective approach for carbon-hydrogen bond activation. This method employs  a transition metal as the C–H activation catalyst  to cleave the C–H bond and attach a carbon, nitrogen, or oxygen​. The ability to selectively functionalize C–H bonds of complex molecules streamlines the organic synthesis process by removing pre-functionalization steps. Moreover, the reliable and predictable conversion of a C–H into a C–C, C–N, C–O or C–X bond in a selective and controlled fashion is a sustainable alternative in diverse synthetic transformations due to waste reduction. C–H activation not only expands the number of sites that can be targeted in a given molecule, multiplying the opportunities for elaboration into more complex products, but also allows for completely different kinds of chemical bonds to be targeted, often with high chemoselectivity.  

We empower your breakthrough synthesis ideas with an unparalleled portfolio of C–H activation catalysts, auxiliaries, and oxidants for the activation of inert and ubiquitous C–H bonds. We offer highly abundant, sustainable metals including cobalt, copper, gold, iridium, iron, nickel, palladium, rhodium, ruthenium, silver, and titanium catalysts with unique reactivity/selectivity to suit your C–H activation needs.  Discover more about our advanced catalyst materials in the C–H Functionalization Guide


Products

catalyst (69)

ligand (9)

oxidant (8)

diversification reagent (4)

linker (2)

surfactant (2)

C-H Activation (69)

C-C Bond Formation (26)

Cross Couplings (7)

Buchwald-Hartwig Cross Coupling Reaction (4)

Heck Reaction (4)

Hiyama Coupling (4)

sulfinic acid (8)

fluoro (6)

amine (2)

carboxylic acid (2)

chloro (2)

iodo (2)
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Potassium persulfate
216224

Potassium persulfate

ACS reagent, ≥99.0%

Hydroxylamine hydrochloride
255580

Hydroxylamine hydrochloride

ACS reagent, 98.0%

Hydrogen peroxide solution
516813

Hydrogen peroxide solution

50 wt. % in H2O, stabilized

<I>tert</I>-Butyl hydroperoxide solution
458139

tert-Butyl hydroperoxide solution

70 wt. % in H2O

Palladium(II) acetate
520764

Palladium(II) acetate

≥99.9% trace metals basis

(1,5-Cyclooctadiene)(methoxy)iridium(I) dimer
685062

(1,5-Cyclooctadiene)(methoxy)iridium(I) dimer

crystals

Periodic acid
375810

Periodic acid

ACS reagent, 99%

(Diacetoxyiodo)benzene
178721

(Diacetoxyiodo)benzene

98%

1-Chloromethyl-4-fluoro-1,4-diazoniabicyclo[2.2.2]octane bis(tetrafluoroborate)
439479

1-Chloromethyl-4-fluoro-1,4-diazoniabicyclo[2.2.2]octane bis(tetrafluoroborate)

>95% in F+ active

2-Picolinic acid
P42800

2-Picolinic acid

ReagentPlus®, 99%

Allylpalladium(II) chloride dimer
222380

Allylpalladium(II) chloride dimer

98%, solid

HS157
683094

HS157

97%, Umicore, powder

Dichloro(<I>p</I>-cymene)ruthenium(II) dimer
343706

Dichloro(p-cymene)ruthenium(II) dimer

Tetra-<I>n</I>-butylammonium decatungstate
900432

Tetra-n-butylammonium decatungstate

powder

Silver acetate
204374

Silver acetate

99.99% trace metals basis

Triruthenium dodecacarbonyl
245011

Triruthenium dodecacarbonyl

99%, crystals

Ruthenium(III) chloride trihydrate
10452

Ruthenium(III) chloride trihydrate

technical grade, solid

Palladium(II) trifluoroacetate
299685

Palladium(II) trifluoroacetate

97%, solid

Pentamethylcyclopentadienylrhodium(III) chloride dimer
338370

Pentamethylcyclopentadienylrhodium(III) chloride dimer

97%, solid

<SC>DL</SC>-α-Tocopherol methoxypolyethylene glycol succinate
763896

DL-α-Tocopherol methoxypolyethylene glycol succinate

powder

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