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palladium catalyst

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Inhibitors & Agonists

Biochemical Assay Reagents

Cat. No.	Product Name	Target	Research Areas	Chemical Structure

HY-Y1738

Tetrakis(triphenylphosphine)palladium Tetrakis(triphenylphosphine)palladium(0)	Biochemical Assay Reagents	Others
Tetrakis(triphenylphosphine)palladium is a catalyst. Tetrakis(triphenylphosphine)palladium catalyzes the highly regioselective addition of phenyl thiocyanate (PhSCN) to terminal alkynes .

HY-W002072

Palladium (II) acetate 2 Publications Verification	Biochemical Assay Reagents	Others
Palladium (II) acetate is a catalyst that catalyzes aromatic substitution reactions .

HY-W018864

Tris(dibenzylideneacetonyl)bis-palladium	Biochemical Assay Reagents	Others
Tris(dibenzylideneacetonyl)bis-palladium is a catalyst that catalyzes the coupling reaction of N-methyl-2-pyrrolidinone (NMP) .

HY-21623

Dichloro[1,1'-bis(diphenylphosphino)ferrocene]palladium(II) dichloromethane adduct	Biochemical Assay Reagents	Others
Dichloro[1,1'-bis(diphenylphosphino)ferrocene]palladium(II) dichloromethane adduct is a common dichloromethane solvate of the palladium catalyst Pd(dppf)Cl₂, a phosphine ligand palladium(II) complex, which can be used as a versatile precatalyst for various cross-coupling reactions. Dichloro[1,1'-bis(diphenylphosphino)ferrocene]palladium(II) dichloromethane adduct can stabilize reaction intermediates and lower the reaction activation energy in coupling reactions, and can be used in Suzuki-Miyaura coupling reaction studies .

HY-W007432

RuPhos	Biochemical Assay Reagents	Others
RuPhos is a Buchwald ligand. In aqueous Suzuki-Miyaura catalytic transfer polymerization, RuPhos forms inactive Pd (RuPhos)₂ with palladium and inhibits diffusion to improve polymerization controllability. RuPhos additional addition in anhydrous Kumada polymerization exacerbates catalyst deactivation and chain transfer, significantly impairing polymerization control .

HY-W048457

Palladium hydroxide on activated carbon(20%)(wetted with ca. 55% Water) Pearlman's catalyst (contains Pd, PdO) (wetted with ca. 55% Water)	Biochemical Assay Reagents	Others
Palladium hydroxide on activated carbon(20%)(wetted with ca. 55% Water) is a biological molecule.

HY-W010686

PdCl2(Amphos)2	Biochemical Assay Reagents	Others
PdCl2(Amphos)2 is a highly efficient palladium catalyst. PdCl2(Amphos)2 can be used in research related to organic synthesis .

HY-W590989

GPhos Pd G6 GPhos Pd G6 TES	Drug Intermediate	Others
GPhos Pd G6 (GPhos Pd G6 TES) is a palladium catalyst. GPhos Pd G6 catalyzes the Buchwald-Hartwig amination reaction and promotes C-N bond formation between aryl chlorides and amines. GPhos Pd G6 is a pharmaceutical intermediate used for the synthesis of various active compounds .

HY-W030778

Nitrilotriacetic acid 1 Publications Verification Triglycollamic acid	Biochemical Assay Reagents	Others
Nitrilotriacetic acid is an orally active chelating agent for metal ions. Nitrilotriacetic acid is an aminotricarboxylic acid that can sequester metal ions as water soluble complexes. Nitrilotriacetic acid reacts with strong oxidizing agents such as hypochlorite, chlorine, ozone, or oxygen in the presence of palladium/carbon catalyst. Nitrilotriacetic acid interacts with solid phases such as cell membranes and bone matrices in the mammalian system. Nitrilotriacetic acid is classified as an epigenetic rodent carcinogen .

HY-W013066

Pd(Xantphos)Cl2	Biochemical Assay Reagents	Others
Pd(Xantphos)Cl2 is a palladium(II) complex catalyst that can be used in organic synthesis research.

HY-158329

Alloc-DOX N-Alloc doxorubicin	Apoptosis Topoisomerase Antibiotic AMPK Bacterial Autophagy Mitophagy HIV HBV	Cancer
Alloc-DOX (N-Alloc doxorubicin) is a Doxorubicin (HY-15142A) prodrug. The combination of a catalyst (such as nano-palladium) and alloc-DOX leads to a decrease in cell viability and tumour growth .

HY-W583317

sSPhos Pd G2	Biochemical Assay Reagents Endogenous Metabolite
sSPhos Pd G2 is a palladium catalyst with excellent cross-coupling reaction activity. sSPhos Pd G2 exhibits efficient catalytic ability in the synthesis of organic molecules and compounds. sSPhos Pd G2 can effectively promote the formation of CC bonds, optimize reaction conditions and increase yields. sSPhos Pd G2 is also used in a variety of transformation reactions, helping researchers develop new materials and compounds.

HY-Y1716

Bis(benzonitrile)palladium chloride Dichlorobis(benzonitrile)palladium(II)	Biochemical Assay Reagents	Others
Bis (benzonitrile) palladium (II) chloride (Dichlorobis (benzonitrile) palladium (II)) serves as a catalyst for the preparation of green amine compounds from terminal olefins .

HY-W020985

Bis[1,2-bis(diphenylphosphino)ethane]palladium(0) Pd(DIPHOS)2	Biochemical Assay Reagents	Others
Bis[1,2-bis(diphenylphosphino)ethane]palladium(0), often abbreviated as Pd(PPh3)2 or Pd(dppf), is an organometallic compound. This compound is widely used as a catalyst for organic chemical reactions, especially cross-coupling reactions such as Suzuki-Miyaura reaction and Heck reaction, and its high catalytic activity, selectivity and stability make it a versatile tool for the synthesis of complex organic compounds , in addition, the potential application of Pd(PPh3)2 in the production of electronic materials and in medical and biochemical research has also been investigated.

HY-W030778R

Nitrilotriacetic acid (Standard) Triglycollamic acid (Standard)	Biochemical Assay Reagents Reference Standards	Others
Nitrilotriacetic acid (Standard) is the analytical standard of Nitrilotriacetic acid. This product is intended for research and analytical applications. Nitrilotriacetic acid is an orally active chelating agent for metal ions. Nitrilotriacetic acid is an aminotricarboxylic acid that can sequester metal ions as water soluble complexes. Nitrilotriacetic acid reacts with strong oxidizing agents such as hypochlorite, chlorine, ozone, or oxygen in the presence of palladium/carbon catalyst. Nitrilotriacetic acid interacts with solid phases such as cell membranes and bone matrices in the mammalian system. Nitrilotriacetic acid is classified as an epigenetic rodent carcinogen .

HY-W543065

CPhos Pd G2	Biochemical Assay Reagents Endogenous Metabolite
CPhos Pd G2 is a highly efficient palladium catalyst with excellent cross-coupling reaction activity. CPhos Pd G2 is widely used in compound synthesis and material science, especially for the construction of complex organic molecules and the synthesis of bioactive compounds. CPhos Pd G2 is also favored for improving reaction selectivity and reducing the formation of by-products.

Cat. No.	Product Name	Type

HY-Y1738

Tetrakis(triphenylphosphine)palladium Tetrakis(triphenylphosphine)palladium(0)	Biochemical Assay Reagents
Tetrakis(triphenylphosphine)palladium is a catalyst. Tetrakis(triphenylphosphine)palladium catalyzes the highly regioselective addition of phenyl thiocyanate (PhSCN) to terminal alkynes .

HY-W002072

Palladium (II) acetate 2 Publications Verification	Biochemical Assay Reagents
Palladium (II) acetate is a catalyst that catalyzes aromatic substitution reactions .

HY-W018864

Tris(dibenzylideneacetonyl)bis-palladium	Biochemical Assay Reagents
Tris(dibenzylideneacetonyl)bis-palladium is a catalyst that catalyzes the coupling reaction of N-methyl-2-pyrrolidinone (NMP) .

HY-21623

Dichloro[1,1'-bis(diphenylphosphino)ferrocene]palladium(II) dichloromethane adduct	Biochemical Assay Reagents
Dichloro[1,1'-bis(diphenylphosphino)ferrocene]palladium(II) dichloromethane adduct is a common dichloromethane solvate of the palladium catalyst Pd(dppf)Cl₂, a phosphine ligand palladium(II) complex, which can be used as a versatile precatalyst for various cross-coupling reactions. Dichloro[1,1'-bis(diphenylphosphino)ferrocene]palladium(II) dichloromethane adduct can stabilize reaction intermediates and lower the reaction activation energy in coupling reactions, and can be used in Suzuki-Miyaura coupling reaction studies .

Dichloro[1,1'-bis(diphenylphosphino)ferrocene]palladium(II) dichloromethane adduct

Biochemical Assay Reagents

Dichloro[1,1'-bis(diphenylphosphino)ferrocene]palladium(II) dichloromethane adduct is a common dichloromethane solvate of the palladium catalyst Pd(dppf)Cl₂, a phosphine ligand palladium(II) complex, which can be used as a versatile precatalyst for various cross-coupling reactions. Dichloro[1,1'-bis(diphenylphosphino)ferrocene]palladium(II) dichloromethane adduct can stabilize reaction intermediates and lower the reaction activation energy in coupling reactions, and can be used in Suzuki-Miyaura coupling reaction studies .

HY-W007432

RuPhos	Biochemical Assay Reagents
RuPhos is a Buchwald ligand. In aqueous Suzuki-Miyaura catalytic transfer polymerization, RuPhos forms inactive Pd (RuPhos)₂ with palladium and inhibits diffusion to improve polymerization controllability. RuPhos additional addition in anhydrous Kumada polymerization exacerbates catalyst deactivation and chain transfer, significantly impairing polymerization control .

HY-W010686

PdCl2(Amphos)2	Biochemical Assay Reagents
PdCl2(Amphos)2 is a highly efficient palladium catalyst. PdCl2(Amphos)2 can be used in research related to organic synthesis .

HY-W013066

Pd(Xantphos)Cl2	Biochemical Assay Reagents
Pd(Xantphos)Cl2 is a palladium(II) complex catalyst that can be used in organic synthesis research.

HY-Y1716

Bis(benzonitrile)palladium chloride Dichlorobis(benzonitrile)palladium(II)	Biochemical Assay Reagents
Bis (benzonitrile) palladium (II) chloride (Dichlorobis (benzonitrile) palladium (II)) serves as a catalyst for the preparation of green amine compounds from terminal olefins .

HY-W020985

Bis[1,2-bis(diphenylphosphino)ethane]palladium(0) Pd(DIPHOS)2	Biochemical Assay Reagents
Bis[1,2-bis(diphenylphosphino)ethane]palladium(0), often abbreviated as Pd(PPh3)2 or Pd(dppf), is an organometallic compound. This compound is widely used as a catalyst for organic chemical reactions, especially cross-coupling reactions such as Suzuki-Miyaura reaction and Heck reaction, and its high catalytic activity, selectivity and stability make it a versatile tool for the synthesis of complex organic compounds , in addition, the potential application of Pd(PPh3)2 in the production of electronic materials and in medical and biochemical research has also been investigated.

Bis[1,2-bis(diphenylphosphino)ethane]palladium(0)

Pd(DIPHOS)2

Biochemical Assay Reagents

Bis[1,2-bis(diphenylphosphino)ethane]palladium(0), often abbreviated as Pd(PPh3)2 or Pd(dppf), is an organometallic compound. This compound is widely used as a catalyst for organic chemical reactions, especially cross-coupling reactions such as Suzuki-Miyaura reaction and Heck reaction, and its high catalytic activity, selectivity and stability make it a versatile tool for the synthesis of complex organic compounds , in addition, the potential application of Pd(PPh3)2 in the production of electronic materials and in medical and biochemical research has also been investigated.

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BODIPY 493/503 purchased from MedChemExpress. Usage Cited in: Nat Commun. 2025 Feb 1;16(1):1241. [Abstract]

MedchemExpress Validation 01

Western blot analysis of extracts from THP-1(lane 2(20μg), Jurkat (lane 3(20μg) and NIH3T3(lane 4(20μg) using FOXO1A (HY-P80132) Rabbit mAb. Proteins were transferred to a PVDF membrane and blocked with 5% non-fat milk in TBST for 2 hour at room temperature. The primary antibody (1/1000) and Loading control antibody (Beta Actin, HY-P80438, 1/10000) was used in 5% non-fat milk in TBST at 4°C overnight. Goat Anti-Mouse/Rabbit IgG-HRP Secondary Antibody (1/10000) was used for 1 hour at room temperature. Western blot analysis of extracts from THP-1(lane 2(20μg), Jurkat (lane 3(20μg) and NIH3T3(lane 4(20μg) using FOXO1A (HY-P80132) Rabbit mAb. Proteins were transferred to a PVDF membrane and blocked with 5% non-fat milk in TBST for 2 hour at room temperature. The primary antibody (1/1000) and Loading control antibody (Beta Actin, HY-P80438, 1/10000) was used in 5% non-fat milk in TBST at 4°C overnight. Goat Anti-Mouse/Rabbit IgG-HRP Secondary Antibody (1/10000) was used for 1 hour at room temperature. Western blot analysis of extracts from THP-1(lane 2(20μg), Jurkat (lane 3(20μg) and NIH3T3(lane 4(20μg) using FOXO1A (HY-P80132) Rabbit mAb. Proteins were transferred to a PVDF membrane and blocked with 5% non-fat milk in TBST for 2 hour at room temperature. The primary antibody (1/1000) and Loading control antibody (Beta Actin, HY-P80438, 1/10000) was used in 5% non-fat milk in TBST at 4°C overnight. Goat Anti-Mouse/Rabbit IgG-HRP Secondary Antibody (1/10000) was used for 1 hour at room temperature.

BODIPY 493/503 purchased from MedChemExpress. Usage Cited in: Nat Commun. 2025 Feb 1;16(1):1241. [Abstract]

MedchemExpress Validation 01

MedchemExpress Validation 03

Western blot analysis of extracts from THP-1(lane 2(20μg), Jurkat (lane 3(20μg) and NIH3T3(lane 4(20μg) using FOXO1A (HY-P80132) Rabbit mAb. Proteins were transferred

MedchemExpress Validation 04

MedchemExpress Validation

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