Benzenediols
Medchemexpress LLC Hydroquinone diacetate (1,4-diacetoxybenzene) | 1205-91-0 | MFCD00011643 | 98.3% | 194.19 g/mol | C10H10O4 | 25 MG
Hydroquinone diacetate (1,4-diacetoxybenzene) is an acetylated derivative of hydroquinone used as a reagent and intermediate in organic and medicinal chemistry. Supplied as a solid powder in small research pack sizes, it is commonly used in synthesis and as an ingredient in skin-lightening formulations. Product documentation includes a data sheet and safety data sheet (SDS).
- Acetylated hydroquinone derivative for synthetic applications.
- Solid powder supplied in small research quantities.
- Molecular formula C10H10O4, molecular weight 194.19 g/mol.
- Typical purity ~98.3%.
- Data sheet and safety data sheet (SDS) available for handling and storage guidance.
Electron Microscopy Sciences Hydroquinone Aqueous Solution, 1% 500 ML
For your convenience in a concentration of 1.0% aqueous.
Medchemexpress LLC 1,2-Benzenediol, 4-methyl- | 452-86-8 | 99.5% | 124.14 | 500 MG
4-Methylcatechol is an intermediate in the degradation of certain alkylbenzenes and an orally active suicide inhibitor of catechol 2,3-dioxygenase (C230). It induces apoptosis in melanoma cells through oxidative stress, and some studies suggest it may be carcinogenic. This compound exhibits antiplatelet and blood pressure-lowering activities, and can inhibit protein oxidation in beef.
- Intermediate in the degradation of certain alkylbenzenes
- Orally active suicide inhibitor of catechol 2,3-dioxygenase (C23O)
- Induces apoptosis in melanoma cells via oxidative stress
- Exhibits antiplatelet activity
- Exhibits blood pressure-lowering activity
- Can inhibit protein oxidation in beef
Medchemexpress LLC 3-Methylcatechol | 488-17-5 | 99.06% | 124.14 | 1 ML
3-Methylcatechol is a phenolic derivative that can be produced by Pseudomonas putida MC2. It can serve as a molecular building block in chemical synthesis to produce other active compounds.
- Phenolic derivative
- Produced by Pseudomonas putida MC2
- Serves as a molecular building block in chemical synthesis
- For research use only
Medchemexpress LLC Catechol violet | 115-41-3 | 90.0% | 250 MG
Catechol violet is an efficient and versatile ligand for Cu(I)-catalyzed C-S coupling reactions. It also functions as a complexometric indicator dye.
- Efficient and versatile ligand for Cu(I)-catalyzed C-S coupling reactions.
- Complexometric indicator dye.
Medchemexpress LLC 4-ethylcatechol | 1124-39-6 | MFCD00015847 | 99.5% | 138.17 | C8H10O2 | 250 MG
4-Ethylcatechol is a ring-dihydroxylated metabolite of 4-ethylphenol used as a biochemical reagent to investigate oxidative DNA damage. It is supplied as a high-purity chemical standard intended for laboratory research applications.
- High purity: 99.5%.
- CAS number: 1124-39-6.
- Chemical formula C8H10O2; molecular weight 138.17.
- Used to study oxidative DNA damage mechanisms.
- Available in small pack sizes including 250 mg for bench-scale experiments.
- Soluble in DMSO, facilitating preparation of stock solutions.
- For research use only; not for human or clinical use.
Sigma Aldrich Fine Chemicals Biosciences (+/-)-Epinephrine hydrochloride | 329-63-5 | MFCD00050562 | 25G
(+/-)-Epinephrine hydrochloride | Mol Wt: 219.67 | 329-63-5 | MFCD00050562 | 25G
![eMolecules 41684-13-3 | N-[1-(4-Methoxyphenyl)ethyl]-N-methylamine | MFCD01123259 | 1g](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502187612.JPG-250.jpg)
eMolecules 41684-13-3 | N-[1-(4-Methoxyphenyl)ethyl]-N-methylamine | MFCD01123259 | 1g
Medchem Express | GGsTop | 5mg | 719836688 | HY-108467 | 926281-37-0 | MFCD27991268 | 331.261 | C13H18NO7P
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eMolecules Building Block Tool<|a>
Cayman Chemical 3-Methoxycatechol 10g
A lignan-derived phenol; a GPR35 agonist (EC50 = 147 µM in a DMR assay) using HT-29 cells; promotes esophageal carcinogenesis in rats at 2% in the diet either alone or in a multiorgan model of nitrosamine-induced carcinogenesis; has been used as a precursor in the enzymatic synthesis of pyrogallol and purpurogallin; has been used as a precursor in the electro-organic synthesis of coumestan derivatives
Medchemexpress LLC 4-Methylcatechol (standard) | 452-86-8 | 97.6% | 124.14 | 100 MG
4-Methylcatechol (Standard) is an analytical standard for research and analytical applications. It functions as an intermediate in alkylbenzene degradation and is an orally active suicide inhibitor of catechol 2,3-dioxygenase (C23O). This compound can induce apoptosis in melanoma cells through oxidative stress and exhibits antiplatelet and blood pressure-lowering activities.
- Analytical standard for research
- Intermediate in alkylbenzene degradation
- Orally active suicide inhibitor of C23O
- Induces apoptosis in melanoma cells
- Antiplatelet and blood pressure-lowering activities
- Used in HPLC, GC, and MS experiments
eMolecules 113638-49-6 | 3-(Trifluoromethoxy)benzene-1,2-diamine | Apollo Scientific | MFCD16628051 | 192.141 | C7H7F3N2O | 97.000 | Nc1cccc(OC(F)(F)F)c1N | 1g | 562428354
3-(Trifluoromethoxy)benzene-1,2-diamine | Apollo Scientific | 113638-49-6 | MFCD16628051 | 192.141 | C7H7F3N2O | 97.000 | Nc1cccc(OC(F)(F)F)c1N | 1g | 562428354
Medchemexpress LLC 4-Methylcatechol (Standard) | 452-86-8 | 97.58% | 124.14 | 25 MG
4-Methylcatechol (Standard) | 452-86-8 | 97.58% | 124.14 | 25 MG
Sigma Aldrich Fine Chemicals Biosciences Isoprenaline hydrochloride | 51-30-9 | MFCD00012603 | 100G
Isoprenaline hydrochloride | Mol Wt: 247.72 | 51-30-9 | MFCD00012603 | 100G
Medchemexpress LLC 4-Methylcatechol | 452-86-8 | MFCD00002205 | 99.5% | 124.14 | 1 ML
4-Methylcatechol is an intermediate involved in the degradation of certain alkylbenzenes and acts as an orally active suicide inhibitor of catechol 2,3-dioxygenase. It has been shown to induce apoptosis in melanoma cells through oxidative stress. While it exhibits antiplatelet and blood pressure-lowering activities, some studies suggest it may have carcinogenic properties.
- Induces cell cycle arrest and apoptosis via the mitochondrial pathway.
- Inhibits protein oxidation in beef.
- Associated with vasodilatory and blood pressure-lowering effects in animal models.
- Has shown carcinogenic effects in forestomach and glandular stomach in rat studies.