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Organocatalyst

" in MedChemExpress (MCE) Product Catalog:

By Targets:	Biochemical Assay Reagents (4) DNA/RNA Synthesis (3) Drug Intermediate (1) Drug Metabolite (2) Fluorescent Dye (1) Fungal (1) Mitochondrial Metabolism (3) Reactive Oxygen Species (ROS) (3) Reference Standards (3)
By Research Areas:	Cancer (3) Infection (1) Neurological Disease (2)

Inhibitors & Agonists

Biochemical Assay Reagents

Natural
Products

Isotope-Labeled Compounds

Cat. No.	Product Name	Target	Research Areas	Chemical Structure

HY-W012218

(±)-Camphor-10-sulfonic acid (±)-10-Camphorsulfonic acid	Biochemical Assay Reagents	Others
(±)-Camphor-10-sulfonic acid is a racemate of Camphor-10-sulfonic acid. (±)-Camphor-10-sulfonic acid can be used as an organocatalyst in performing a huge array of organic transformations .

HY-W001187

Tempo 5+ Cited Publications	Mitochondrial Metabolism DNA/RNA Synthesis Reactive Oxygen Species (ROS)	Cancer
Tempo is a nitric oxide radical and a selective scavenger of ROS in mitochondria. Tempo is also an organocatalyst that disproportionates superoxide and oxidizes primary alcohols to aldehydes in a catalytic cycle. Tempo has mutagenic and antioxidant effects and can induceDNA strand breaks. Tempo also exerts cytotoxic and mutagenic properties in mouse lymphoma cells .

HY-W015788

1-Phenylethane-1,2-diol Styrene Glycol	Biochemical Assay Reagents Drug Metabolite	Neurological Disease
1-Phenylethane-1,2-diol (Styrene Glycol) is a benzyl diol compound, which is the major metabolite of Styrene. 1-Phenylethane-1,2-diol can be oxidized to hydroxyl ketone (2-hydroxy-1-phenylethan-1-one) selectively with variety of catalysts, including organocatalysts, metal complexes, non-noble metal oxides, bimetallics .

HY-I0259

8-Amino-2-naphthol	Fluorescent Dye	Others
8-Amino-2-naphthol is a photoactive charge transfer compounds, which can be used as fluorescent probe. 8-Amino-2-naphthol undergoes excited-state proton transfer (ESPT) to form a zwitterion under acidic conditions, where the photoacidity of its hydroxyl group is regulated by the protonation state of the amino group, enabling pH to act as an on/off switch for photoacidity. 8-Amino-2-naphthol is also utilized as chiral organocatalyst .

HY-W012218R

(±)-Camphor-10-sulfonic acid (Standard) (±)-10-Camphorsulfonic acid (Standard)	Reference Standards Biochemical Assay Reagents	Others
(±)-Camphor-10-sulfonic acid (Standard) is the analytical standard of (±)-Camphor-10-sulfonic acid. This product is intended for research and analytical applications. (±)-Camphor-10-sulfonic acid is a racemate of Camphor-10-sulfonic acid. (±)-Camphor-10-sulfonic acid can be used as an organocatalyst in performing a huge array of organic transformations .

HY-W272811

Camphorsulfonate sodium	Drug Intermediate Fungal	Infection
Camphorsulfonate sodium is an organic synthesis intermediate. Camphorsulfonate sodium can be used for synthesis of derivatives with SDH inhibitory activity through scaffold hopping. Camphorsulfonate sodium is also an organocatalyst that can be used as a pore-forming additive for modulating the porosity of the graphene film. Camphorsulfonate sodium can be used for binder-free porous graphene film and fungicide research .

HY-W001187S

Tempo-d18	DNA/RNA Synthesis Mitochondrial Metabolism Reactive Oxygen Species (ROS)	Cancer
Tempo-d₁₈ is the deuterium labeled Tempo . Tempo is a classic nitroxide radical and is a selective scavenger of ROS that dismutases superoxide in the catalytic cycle. Tempo induces DNA-strand breakage. Tempo can be used as an organocatalyst for the oxidation of primary alcohols to aldehydes. Tempo has mutagenic and antioxidant effects .

HY-W001187R

Tempo (Standard)	Mitochondrial Metabolism DNA/RNA Synthesis Reactive Oxygen Species (ROS) Reference Standards	Cancer
Tempo (Standard) is the analytical standard of Tempo. This product is intended for research and analytical applications. Tempo is a nitric oxide radical and a selective scavenger of ROS in mitochondria. Tempo is also an organocatalyst that disproportionates superoxide and oxidizes primary alcohols to aldehydes in a catalytic cycle. Tempo has mutagenic and antioxidant effects and can induceDNA strand breaks. Tempo also exerts cytotoxic and mutagenic properties in mouse lymphoma cells [4].

HY-W015788R

1-Phenylethane-1,2-diol (Standard) Styrene Glycol (Standard)	Biochemical Assay Reagents Reference Standards Drug Metabolite	Neurological Disease
1-Phenylethane-1,2-diol (Standard) is the analytical standard of 1-Phenylethane-1,2-diol. This product is intended for research and analytical applications. 1-Phenylethane-1,2-diol (Styrene Glycol) is a benzyl diol compound, which is the major metabolite of Styrene. 1-Phenylethane-1,2-diol can be oxidized to hydroxyl ketone (2-hydroxy-1-phenylethan-1-one) selectively with variety of catalysts, including organocatalysts, metal complexes, non-noble metal oxides, bimetallics[1][2][3].

Cat. No.	Product Name	Type

HY-W012218

(±)-Camphor-10-sulfonic acid (±)-10-Camphorsulfonic acid	Biochemical Assay Reagents
(±)-Camphor-10-sulfonic acid is a racemate of Camphor-10-sulfonic acid. (±)-Camphor-10-sulfonic acid can be used as an organocatalyst in performing a huge array of organic transformations .

HY-I0259

8-Amino-2-naphthol	Biochemical Assay Reagents
8-Amino-2-naphthol is a photoactive charge transfer compounds, which can be used as fluorescent probe. 8-Amino-2-naphthol undergoes excited-state proton transfer (ESPT) to form a zwitterion under acidic conditions, where the photoacidity of its hydroxyl group is regulated by the protonation state of the amino group, enabling pH to act as an on/off switch for photoacidity. 8-Amino-2-naphthol is also utilized as chiral organocatalyst .

8-Amino-2-naphthol

Biochemical Assay Reagents

8-Amino-2-naphthol is a photoactive charge transfer compounds, which can be used as fluorescent probe. 8-Amino-2-naphthol undergoes excited-state proton transfer (ESPT) to form a zwitterion under acidic conditions, where the photoacidity of its hydroxyl group is regulated by the protonation state of the amino group, enabling pH to act as an on/off switch for photoacidity. 8-Amino-2-naphthol is also utilized as chiral organocatalyst .

HY-W012218R

(±)-Camphor-10-sulfonic acid (Standard) (±)-10-Camphorsulfonic acid (Standard)	Biochemical Assay Reagents
(±)-Camphor-10-sulfonic acid (Standard) is the analytical standard of (±)-Camphor-10-sulfonic acid. This product is intended for research and analytical applications. (±)-Camphor-10-sulfonic acid is a racemate of Camphor-10-sulfonic acid. (±)-Camphor-10-sulfonic acid can be used as an organocatalyst in performing a huge array of organic transformations .

Cat. No.	Product Name	Category	Target	Chemical Structure

HY-W015788

1-Phenylethane-1,2-diol Styrene Glycol	Natural Products Microorganisms Classification of Application Fields Other Diseases Disease Research Fields	Biochemical Assay Reagents Drug Metabolite
1-Phenylethane-1,2-diol (Styrene Glycol) is a benzyl diol compound, which is the major metabolite of Styrene. 1-Phenylethane-1,2-diol can be oxidized to hydroxyl ketone (2-hydroxy-1-phenylethan-1-one) selectively with variety of catalysts, including organocatalysts, metal complexes, non-noble metal oxides, bimetallics .

HY-W015788R

1-Phenylethane-1,2-diol (Standard) Styrene Glycol (Standard)	Natural Products Microorganisms	Biochemical Assay Reagents Reference Standards Drug Metabolite
1-Phenylethane-1,2-diol (Standard) is the analytical standard of 1-Phenylethane-1,2-diol. This product is intended for research and analytical applications. 1-Phenylethane-1,2-diol (Styrene Glycol) is a benzyl diol compound, which is the major metabolite of Styrene. 1-Phenylethane-1,2-diol can be oxidized to hydroxyl ketone (2-hydroxy-1-phenylethan-1-one) selectively with variety of catalysts, including organocatalysts, metal complexes, non-noble metal oxides, bimetallics[1][2][3].

Cat. No.	Product Name	Chemical Structure

HY-W001187S

Tempo-d18
Tempo-d₁₈ is the deuterium labeled Tempo . Tempo is a classic nitroxide radical and is a selective scavenger of ROS that dismutases superoxide in the catalytic cycle. Tempo induces DNA-strand breakage. Tempo can be used as an organocatalyst for the oxidation of primary alcohols to aldehydes. Tempo has mutagenic and antioxidant effects .

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Organocatalyst

Inhibitors & Agonists

Biochemical Assay Reagents

NaturalProducts

Isotope-Labeled Compounds

Natural
Products