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organic matter

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By Targets:	Apoptosis (1) Bacterial (1) Biochemical Assay Reagents (7) DNA/RNA Synthesis (1) Drug Derivative (1) Drug Intermediate (2) Drug Metabolite (1) Environmental Pollutants (6) Fluorescent Dye (2) Isotope-Labeled Compounds (2) MDM-2/p53 (1) Reference Standards (4) SOD (1)
By Research Areas:	Cancer (3) Infection (1) Inflammation/Immunology (1) Neurological Disease (1)

Inhibitors & Agonists

Fluorescent Dyes

Natural
Products

Isotope-Labeled Compounds

Targets Recommended: OAT MOFs

Cat. No.	Product Name	Target	Research Areas	Chemical Structure

HY-N13022

Humic acid 1 Publications Verification	Environmental Pollutants Bacterial SOD	Inflammation/Immunology Cancer
Humic acid is an important component of organic matter in soil and water, and serves as a plant regulator. Humic acid has multiple reactive activities such as surface adsorption, ion exchange, and complexation. Humic acid can enhance pyrene degradation by Mycobacterium NJS-1. Humic acid can inhibit the activity of superoxide dismutase and scavenge hydroxyl radicals. Humic acid is also toxic to CEM cells .

HY-128454

Dimethyl trisulfide	Environmental Pollutants Biochemical Assay Reagents	Infection Neurological Disease
Dimethyl trisulfide is a cyanide scavenger. Dimethyl trisulfide can be isolated from garlic, onions, broccoli and similar plants. Dimethyl trisulfide converts cyanide into thiocyanate. Dimethyl trisulfide is used by saprophagous insects to locate breeding sites (decaying organic matter), and is also used by deceptive flowers in brood sites to attract such insects. Dimethyl trisulfide induces electrophysiological responses in houseflies .

HY-103609

Pyrene 1 Publications Verification Benzo[def]phenanthrene	Environmental Pollutants Biochemical Assay Reagents	Others
Pyrene is a polycyclic aromatic hydrocarbon (PAH) composed of four fused benzene rings. It has a distinct aromatic odor, produced by incomplete combustion of organic matter. Pyrene exhibits strong fluorescence, emitting in the blue region of the spectrum, making it useful as a probe for studying molecular interactions in solution and on surfaces. Pyrene is also used as a model compound for the study of PAHs in various environments and biological systems because of its ubiquity in these environments. However, long-term exposure to pyrene has been associated with potential health risks, including carcinogenicity and mutagenicity.

HY-W013053

Dibenz[a,h]anthracene DBA; 1,2,5,6-Dibenzanthracene; Benzo[k]tetraphene	Environmental Pollutants DNA/RNA Synthesis MDM-2/p53 Apoptosis	Cancer
Dibenz[a,h]anthracene (DBA) is an orally active polycyclic aromatic hydrocarbon, a by-product of incomplete combustion of organic matter, a potent carcinogen, and an agonist of AhR. Dibenz[a,h]anthracene induces dose-dependent increases in DNA adduct formation and lacZ mutation frequency. Dibenz[a,h]anthracene upregulates St3gal5. Dibenz[a,h]anthracene can be used in cancer-related research .

HY-W086988

5-Methyl-1H-benzotriazole 5-Methylbenzotriazole	Biochemical Assay Reagents	Others
5-Methyl-1H-benzotriazole (5-Methylbenzotriazole) is a benzotriazole derivative, and serves as a key building block for ultraviolet absorbers and light stabilizers. 5-Methyl-1H-benzotriazole reduces the photosensitizing ability of nitrate and dissolved organic matter (DOM), enhances the persistence of microorganic pollutants, inhibits the photodegradation of DOM and drug residues, and quenches the triplet excited states of DOM and methotrexate substructures. 5-Methyl-1H-benzotriazole acts as a corrosion inhibitor for copper and copper alloys, and is present in formulations of anti-icing fluids, dishwasher detergents, aircraft deicing fluids and automotive antifreezes .

HY-W013570

Acenaphthylene 1 Publications Verification	Environmental Pollutants Drug Intermediate	Others
Acenaphthylene is a polycyclic aromatic hydrocarbon (PAH). PAHs are derived naturally from coal and tar deposits, and produced by incomplete combustion of organic matter .

HY-W038786

2,4,6-Trimethylphenol	Environmental Pollutants Fluorescent Dye	Others
2,4,6-Trimethylphenol is a probe compound shown to react mainly with organic matter ( ³DOM ^*). 2,4,6-Trimethylphenol is rapidly oxidized by singlet oxygen in aqueous solution .

HY-W013570S

Acenaphthylene-d8 Acenaphthylene-d₈	Isotope-Labeled Compounds	Others
Acenaphthylene-d₈ is the deuterium labeled Acenaphthylene . Acenaphthylene is a polycyclic aromatic hydrocarbon (PAH). PAHs are derived naturally from coal and tar deposits, and produced by incomplete combustion of organic matter .

HY-W112021

2,5-DMBQ 2,5-Dimethoxybenzoquinone	Biochemical Assay Reagents	Others
2,5-DMBQ (2,5-Dimethoxybenzoquinone) serves as an extracellular reductant. 2,5-DMBQ is involved in a crucial redox cycle, namely the extracellular hydroquinone-quinone redox cycle. In this cycle, 2,5-DMBQ is capable of reducing extracellular Fe ^³⁺ and generating H₂O₂. 2,5-DMBQ plays a pivotal role in the biodegradation mechanism of brown rot fungal, assisting the fungi in decomposing and utilizing organic matter .

HY-W013570R

Acenaphthylene (Standard)	Reference Standards Others	Others
Acenaphthylene (Standard) is the analytical standard of Acenaphthylene. This product is intended for research and analytical applications. Acenaphthylene is a polycyclic aromatic hydrocarbon (PAH). PAHs are derived naturally from coal and tar deposits, and produced by incomplete combustion of organic matter .

HY-W038786S

2,4,6-Trimethylphenol-d11	Isotope-Labeled Compounds	Others
2,4,6-Trimethylphenol-d₁₁ is the deuterium labeled 2,4,6-Trimethylphenol . 2,4,6-Trimethylphenol is a probe compound shown to react mainly with organic matter (3DOM*). 2,4,6-Trimethylphenol is rapidly oxidized by singlet oxygen in aqueous solution .

HY-W112021R

2,5-DMBQ (Standard) 2,5-Dimethoxybenzoquinone (Standard)	Biochemical Assay Reagents Reference Standards	Others
2,5-DMBQ (2,5-Dimethoxybenzoquinone) serves as an extracellular reductant. 2,5-DMBQ is involved in a crucial redox cycle, namely the extracellular hydroquinone-quinone redox cycle. In this cycle, 2,5-DMBQ is capable of reducing extracellular Fe³⁺ and generating H2O2. 2,5-DMBQ plays a pivotal role in the biodegradation mechanism of brown rot fungal, assisting the fungi in decomposing and utilizing organic matter .

HY-103609R

Pyrene (Standard) Benzo[def]phenanthrene (Standard)	Biochemical Assay Reagents Reference Standards	Others
Pyrene (Standard) is the analytical standard of Pyrene. This product is intended for research and analytical applications. Pyrene is a polycyclic aromatic hydrocarbon (PAH) composed of four fused benzene rings. It has a distinct aromatic odor, produced by incomplete combustion of organic matter. Pyrene exhibits strong fluorescence, emitting in the blue region of the spectrum, making it useful as a probe for studying molecular interactions in solution and on surfaces. Pyrene is also used as a model compound for the study of PAHs in various environments and biological systems because of its ubiquity in these environments. However, long-term exposure to pyrene has been associated with potential health risks, including carcinogenicity and mutagenicity.

HY-N16496

17-Oxoheptadecanoic acid	Others	Others
17-Oxoheptadecanoic acid is a ω-oxocarboxylic acid with a carbon chain length of 17 carbon atoms. 17-Oxoheptadecanoic acid can be as a tracer for atmospheric source organic matter .

HY-W096907

Picene	Biochemical Assay Reagents	Cancer
Picene is a polycyclic aromatic hydrocarbon of environmental relevance. Picene can be widely distributed in the environment as the result of incomplete combustion of organic matter. Picene is found to be inactive as complete carcinogen, while it acts in a high dose as a weak tumor initiator .

HY-W038786R

2,4,6-Trimethylphenol (Standard)	Fluorescent Dye Reference Standards	Others
2,4,6-Trimethylphenol (Standard) is the analytical standard of 2,4,6-Trimethylphenol. This product is intended for research and analytical applications. 2,4,6-Trimethylphenol is a probe compound shown to react mainly with organic matter (3DOM*). 2,4,6-Trimethylphenol is rapidly oxidized by singlet oxygen in aqueous solution[1][2].

HY-W286414

N,N-dimethyl-N'-p-tolylsulfamide DMST	Drug Derivative	Others
N,N-dimethyl-N'-p-tolylsulfamide (DMST) is a hydrolysis product of Tolylfluanid (HY-W774955). The photodegradation rate of N,N-dimethyl-N'-p-tolylsulfamide in coastal seawater is higher than that in seawater or deionized water .

HY-W714180

Desmethyl-formamido-pirimicarb	Drug Metabolite Drug Intermediate	Others
Desmethyl-formamido-pirimicarb is an intermediate metabolite of Pirimicarb (HY-119419). Desmethyl-formamido-pirimicarb is detected in both Pirimicarb-exposed soil environments and advanced oxidation water treatment processes .

Cat. No.	Product Name	Type

HY-103609

Pyrene 1 Publications Verification Benzo[def]phenanthrene	Fluorescent Dyes
Pyrene is a polycyclic aromatic hydrocarbon (PAH) composed of four fused benzene rings. It has a distinct aromatic odor, produced by incomplete combustion of organic matter. Pyrene exhibits strong fluorescence, emitting in the blue region of the spectrum, making it useful as a probe for studying molecular interactions in solution and on surfaces. Pyrene is also used as a model compound for the study of PAHs in various environments and biological systems because of its ubiquity in these environments. However, long-term exposure to pyrene has been associated with potential health risks, including carcinogenicity and mutagenicity.

Pyrene

1 Publications Verification

Benzo[def]phenanthrene

Fluorescent Dyes

Pyrene is a polycyclic aromatic hydrocarbon (PAH) composed of four fused benzene rings. It has a distinct aromatic odor, produced by incomplete combustion of organic matter. Pyrene exhibits strong fluorescence, emitting in the blue region of the spectrum, making it useful as a probe for studying molecular interactions in solution and on surfaces. Pyrene is also used as a model compound for the study of PAHs in various environments and biological systems because of its ubiquity in these environments. However, long-term exposure to pyrene has been associated with potential health risks, including carcinogenicity and mutagenicity.

HY-103609R

Pyrene (Standard) Benzo[def]phenanthrene (Standard)	Fluorescent Dyes
Pyrene (Standard) is the analytical standard of Pyrene. This product is intended for research and analytical applications. Pyrene is a polycyclic aromatic hydrocarbon (PAH) composed of four fused benzene rings. It has a distinct aromatic odor, produced by incomplete combustion of organic matter. Pyrene exhibits strong fluorescence, emitting in the blue region of the spectrum, making it useful as a probe for studying molecular interactions in solution and on surfaces. Pyrene is also used as a model compound for the study of PAHs in various environments and biological systems because of its ubiquity in these environments. However, long-term exposure to pyrene has been associated with potential health risks, including carcinogenicity and mutagenicity.

Pyrene (Standard)

Benzo[def]phenanthrene (Standard)

Fluorescent Dyes

Pyrene (Standard) is the analytical standard of Pyrene. This product is intended for research and analytical applications. Pyrene is a polycyclic aromatic hydrocarbon (PAH) composed of four fused benzene rings. It has a distinct aromatic odor, produced by incomplete combustion of organic matter. Pyrene exhibits strong fluorescence, emitting in the blue region of the spectrum, making it useful as a probe for studying molecular interactions in solution and on surfaces. Pyrene is also used as a model compound for the study of PAHs in various environments and biological systems because of its ubiquity in these environments. However, long-term exposure to pyrene has been associated with potential health risks, including carcinogenicity and mutagenicity.

Cat. No.	Product Name	Category	Target	Chemical Structure

HY-N13022

Humic acid 1 Publications Verification	Structural Classification Natural Products Plants Source Classification	Environmental Pollutants Bacterial SOD
Humic acid is an important component of organic matter in soil and water, and serves as a plant regulator. Humic acid has multiple reactive activities such as surface adsorption, ion exchange, and complexation. Humic acid can enhance pyrene degradation by Mycobacterium NJS-1. Humic acid can inhibit the activity of superoxide dismutase and scavenge hydroxyl radicals. Humic acid is also toxic to CEM cells .

HY-128454

Dimethyl trisulfide	Structural Classification Natural Products Microorganisms Liliaceae Classification of Application Fields Other Diseases Plants Endogenous metabolite Disease Research Fields A．Sativam L. var．Viviparum Regel Source Classification	Environmental Pollutants Biochemical Assay Reagents
Dimethyl trisulfide is a cyanide scavenger. Dimethyl trisulfide can be isolated from garlic, onions, broccoli and similar plants. Dimethyl trisulfide converts cyanide into thiocyanate. Dimethyl trisulfide is used by saprophagous insects to locate breeding sites (decaying organic matter), and is also used by deceptive flowers in brood sites to attract such insects. Dimethyl trisulfide induces electrophysiological responses in houseflies .

HY-W013570

Acenaphthylene 1 Publications Verification	Structural Classification Natural Products other families Classification of Application Fields Other Diseases Plants Disease Research Fields Source Classification	Environmental Pollutants Drug Intermediate
Acenaphthylene is a polycyclic aromatic hydrocarbon (PAH). PAHs are derived naturally from coal and tar deposits, and produced by incomplete combustion of organic matter .

HY-W038786

2,4,6-Trimethylphenol	Structural Classification Monophenols Classification of Application Fields Other Diseases Phenols Endogenous metabolite Disease Research Fields Source Classification	Environmental Pollutants Fluorescent Dye
2,4,6-Trimethylphenol is a probe compound shown to react mainly with organic matter ( ³DOM ^*). 2,4,6-Trimethylphenol is rapidly oxidized by singlet oxygen in aqueous solution .

HY-W013570R

Acenaphthylene (Standard)	Structural Classification Natural Products other families Plants Source Classification	Reference Standards Others
Acenaphthylene (Standard) is the analytical standard of Acenaphthylene. This product is intended for research and analytical applications. Acenaphthylene is a polycyclic aromatic hydrocarbon (PAH). PAHs are derived naturally from coal and tar deposits, and produced by incomplete combustion of organic matter .

HY-N16496

17-Oxoheptadecanoic acid	Structural Classification Microorganisms Ketones, Aldehydes, Acids Source Classification	Others
17-Oxoheptadecanoic acid is a ω-oxocarboxylic acid with a carbon chain length of 17 carbon atoms. 17-Oxoheptadecanoic acid can be as a tracer for atmospheric source organic matter .

HY-W038786R

2,4,6-Trimethylphenol (Standard)	Structural Classification Monophenols Phenols Endogenous metabolite Source Classification	Fluorescent Dye Reference Standards
2,4,6-Trimethylphenol (Standard) is the analytical standard of 2,4,6-Trimethylphenol. This product is intended for research and analytical applications. 2,4,6-Trimethylphenol is a probe compound shown to react mainly with organic matter (3DOM*). 2,4,6-Trimethylphenol is rapidly oxidized by singlet oxygen in aqueous solution[1][2].

Cat. No.	Product Name	Chemical Structure

HY-W013570S

Acenaphthylene-d8
Acenaphthylene-d₈ is the deuterium labeled Acenaphthylene . Acenaphthylene is a polycyclic aromatic hydrocarbon (PAH). PAHs are derived naturally from coal and tar deposits, and produced by incomplete combustion of organic matter .

HY-W038786S

2,4,6-Trimethylphenol-d11
2,4,6-Trimethylphenol-d₁₁ is the deuterium labeled 2,4,6-Trimethylphenol . 2,4,6-Trimethylphenol is a probe compound shown to react mainly with organic matter (3DOM*). 2,4,6-Trimethylphenol is rapidly oxidized by singlet oxygen in aqueous solution .

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organic matter

Inhibitors & Agonists

Fluorescent Dyes

NaturalProducts

Isotope-Labeled Compounds

Natural
Products