Phenols
Medchemexpress LLC 1-bromo-2-methyl-3-nitrobenzene | 55289-35-5 | MFCD00009792 | 99.5% | 216.03 g/mol | C7H6BrNO2 | 25 G
1-Bromo-2-methyl-3-nitrobenzene is an aromatic organic intermediate used in medicinal and synthetic chemistry. Its bromine substituent serves as a leaving group for cross-coupling and nucleophilic substitution reactions, while the nitro group provides electron-withdrawing directing effects. It is commonly used as a precursor for constructing more complex aromatic scaffolds.
- Enables cross-coupling and substitution reactions
- Nitro group provides electron-withdrawing directing effects
- High purity suitable for research applications
- Supplied in multiple package sizes for scalability
- Stable when stored under recommended conditions
Medchemexpress LLC Sodium benzenesulfonate | 515-42-4 | MFCD00065179 | >96.0% | 180.16 g/mol | C6H5NaO3S | 500 G
Sodium benzenesulfonate (CAS 515-42-4) is the sodium salt of benzenesulfonic acid used as a biochemical reagent and analytical standard. It is supplied as a white to off-white solid for research and analytical applications requiring a sulfonated aromatic salt.
- Chemical formula C6H5NaO3S, molecular weight 180.16 g/mol.
- White to off-white solid appearance.
- Purity greater than 96.0% (HPLC) for reagent-grade material.
- Available in multiple packaging sizes, including 500 g.
- Commonly used as a reagent and analytical standard in research applications.
![Medchemexpress LLC 3-[(1S)-1-(dimethylamino)ethyl]phenol | 139306-10-8 | MFCD06656491 | 99.0% | 165.23 g·mol⁻1 | C10H15NO | 25 G](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000303356.png-250.jpg)
Medchemexpress LLC 3-[(1S)-1-(dimethylamino)ethyl]phenol | 139306-10-8 | MFCD06656491 | 99.0% | 165.23 g·mol⁻1 | C10H15NO | 25 G
Rivastigmine metabolite (NAP 226-90), 3-[(1S)-1-(dimethylamino)ethyl]phenol, is the primary active metabolite of rivastigmine and acts as an acetylcholinesterase (AChE) inhibitor. Supplied as a white to off-white solid reference standard, it is intended for biochemical research, Alzheimer's disease studies, and analytical applications requiring a characterized metabolite standard.
- High purity (99.01%) suitable for analytical and reference use.
- Well-defined chemical identity: C10H15NO, molecular weight 165.23 g·mol⁻1.
- Solid form with clear appearance for straightforward handling and storage.
- Recommended storage conditions provided for long-term stability.
- Available in multiple package sizes to support both small-scale and larger studies.
Medchemexpress LLC 8-bromo-cAMP sodium salt | 76939-46-3 | MFCD00005844 | 99.9% | 430.08 | C10H10BrN5NaO6P | 25MG
8-Bromo-cAMP sodium salt is a membrane-permeable analog of cyclic adenosine monophosphate (cAMP) that activates cyclic AMP-dependent protein kinase (PKA). It is used in biochemical and cell biology research to mimic cAMP signaling and probe PKA-mediated pathways involved in regulation of proliferation, differentiation, and apoptosis. Supplied as a sodium salt powder with high purity suitable for in vitro assays.
- Cell-permeable cAMP analog for intracellular signaling studies.
- Activates cyclic AMP-dependent protein kinase (PKA).
- High purity suitable for biochemical and cellular assays.
- Stable sodium salt form for convenient handling and solution preparation.
- Available in small quantities for lab-scale experiments (e.g., 25 mg).
Medchemexpress LLC Luseogliflozin hydrate | 1152425-66-5 | 99.2% | 452.56 g/mol | C23H32O7S | 25 MG
Luseogliflozin hydrate is a research-grade sodium-glucose cotransporter 2 (SGLT2) inhibitor provided as the hydrate form. It is a potent and selective compound used in preclinical studies of glucose homeostasis and type 2 diabetes mellitus. The material is supplied as a high-purity solid suitable for in vitro and in vivo research applications.
- Potent SGLT2 inhibition (IC50 ≈ 2.26 nM).
- High purity (99.2%) suitable for research use.
- Hydrate form for consistent physicochemical properties.
- Molecular weight 452.56 g/mol; formula C23H32O7S.
- White to off-white solid, typically supplied in 25 MG quantities.
- Suitable for in vitro and in vivo studies of glucose transport and metabolism.
Medchemexpress LLC Bromophenol blue sodium salt | 34725-61-6 | MFCD00013793 | 691.94 | C19H9Br4NaO5S | 10 G
Bromophenol blue sodium salt is a sodium salt form of the pH indicator bromophenol blue supplied as a solid biochemical reagent for laboratory use. It is commonly used as a tracking dye and pH indicator in electrophoresis and buffer applications.
- pH indicator and tracking dye for electrophoresis
- Sodium salt solid form for buffer compatibility
- Soluble in aqueous buffers used in nucleic acid and protein gels
- Available in multiple pack sizes, including 10 g
- Provided with datasheet, COA, and SDS on the manufacturer site
Medchemexpress LLC LV-320 | 2449093-46-1 | 95.0% | 520.11 | 1 ML
LV-320 is a potent and uncompetitive ATG4B inhibitor with an IC50 of 24.5 μM and a Kd of 16 μM. It inhibits ATG4B enzymatic activity, blocks autophagic flux in cells, and is stable, non-toxic, and active in vivo.
- Increases endogenous LC3B-II and protein p62 levels in SKBR3, MCF7, JIMT1, and MDA-MB-231 cells in a dose-dependent manner.
- Blocks autophagic flux in MDA-MB-231 cells.
- Achieves terminal blood levels of 169 μM and liver levels of 104 μM in GFP-LC3 mice following oral gavage.
- Significantly increases the accumulation of GFP-LC3 puncta and LC3B-II protein in treated animals without causing significant toxicity at tested doses.
Medchemexpress LLC Melamine | 108-78-1 | MFCD00006055 | 100.0% | 126.12 g/mol | C3H6N6 | 100g
Melamine is an orally active inducer of Apoptosis Melamine induces animal disease models Melamine affects the activity of Sertoli cell and can be used for research on male reproductive function Melamine also has neurotoxicity and nephrotoxicity Melamine induces cognitive impairment and acute kidney injury models Melamine can also be used to induce bladder cancer and urinary stone models[1][2][3][4][5][6]
![Medchemexpress LLC 2-Furancarboxamide, 3-(3,4-difluoro-2-methoxyphenyl)-N-[6-[(1R)-1,2-dihydroxyethyl]-3-pyridinyl... | 2877755-11-6 | 929055 | 99.9% | 490.42 | 1 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000386454-logo.png-250.jpg){kind=logo}
Medchemexpress LLC 2-Furancarboxamide, 3-(3,4-difluoro-2-methoxyphenyl)-N-[6-[(1R)-1,2-dihydroxyethyl]-3-pyridinyl... | 2877755-11-6 | 929055 | 99.9% | 490.42 | 1 MG
Sodium Channel inhibitor 6 (compound I) is a selective Nav1.8 inhibitor that can be used in the study of neuropathic pain. It is an intermediate for synthesizing potent Nav1.8 inhibitors. This product is for research use only.
- Selective Nav1.8 inhibitor.
- Used in the study of neuropathic pain.
- Intermediate for synthesizing potent Nav1.8 inhibitors.
- High purity: 99.93%.
Apexbio Technology LLC Rabeprazole sodium 117976-90-6 10mM (in 1mL DMSO)
Rabeprazole sodium (CAS 117976-90-6) is a small-molecule inhibitor targeting gastric H /K -ATPase It is designed to irreversibly inhibit this proton pump enzyme thereby suppressing gastric acid secretion Rabeprazole sodium exerts its biological activity primarily through irreversible inhibition of H /K -ATPase It also induces apoptosis and inhibits uridine nucleoside hydrolase (UNH) with an IC50 value of 0 3 M Based on these pharmacological properties Rabeprazole sodium holds research potential in studies of gastric ulcer gastroesophageal reflux disease and the investigation of proton pump inhibition apoptosis induction and nucleoside metabolism regulation
Medchemexpress LLC N-lauryldiethanolamine | 1541-67-9 | MFCD00059002 | >95.0% | 273.45 g/mol | C16H35NO2 | 100 G
N-Lauryldiethanolamine is an aliphatic tertiary amine used as an antistatic agent and surfactant. Supplier listings report bioactivity including inhibitory effects on cell growth and lysosomotropic behavior; consult safety data sheets for handling and toxicity information.
- Antistatic agent and surfactant
- Aminodiol structure; molecular formula C16H35NO2
- Molecular weight 273.45 g/mol
- CAS number 1541-67-9
- Typically supplied in 100 G packages
- Common purity: >95.0% (GC)
Medchemexpress LLC Ponceau S, sodium salt | 6226-79-5 | MFCD00003892 | 75.0% | 760.57 g/mol | C22H12N4Na4O13S4 | 25G
Ponceau S (sodium salt) is a water-soluble azo dye used for rapid, reversible staining of proteins on nitrocellulose, PVDF, and cellulose acetate membranes. Supplied as a powder for solution preparation, it is commonly used to visualize protein bands during membrane transfer checks and prior to immunodetection workflows, and can be removed without affecting downstream analyses.
- Provides rapid, reversible staining of protein bands on membranes.
- Compatible with nitrocellulose, PVDF, and cellulose acetate membranes.
- Water-soluble dye formulated for acidic staining solutions.
- Supplied as a powder for on-demand solution preparation and storage.
- Typical dye content 75% for routine visualization.
- Removes easily to permit subsequent immunodetection steps.
Medchemexpress LLC Nicotinohydrazide | 553-53-7 | 99.35% | 137.14 | 100 G
Nicotinohydrazide (Nicotinic acid hydrazide) is a small molecular compound used for research purposes. It exhibits cytotoxic activity and trypanosomicidal activity, making it suitable for various biological studies.
- Exhibits cytotoxic activity against human HeLa cells (CC50 of 153 μg/mL after 24 hours incubation).
- Shows trypanosomicidal activity against the amastigote stage of Trypanosoma cruzi Tulahuen C4 in Vero cells (IC50 > 73 μM after 5 days of incubation).
- Can be stored as powder at -20°C for 3 years or 4°C for 2 years.
- Can be stored in solvent at -80°C for 2 years or -20°C for 1 year.
- Soluble in DMSO (100 mg/mL).
Medchemexpress LLC Methylisothiazolinone hydrochloride | 26172-54-3 | 99.4% | 151.61 | 25 G
Methylisothiazolinone hydrochloride is a bacterial and fungal inhibitor and preservative, also acting as a sensitizer. It activates matrix metalloproteinases (MMPs) in human bronchial epithelial cells, leading to apoptosis and inflammatory responses. This compound can also promote the development of atopic dermatitis in mice by disrupting Th2/Th17 related immune responses and cause mitochondrial damage in the endothelium of rat cerebral blood vessels.
- Acts as a bacterial and fungal inhibitor and preservative
- Induces cell apoptosis and inflammatory response
- Activates matrix metalloproteinases (MMPs)
- Promotes atopic dermatitis development in mice
- Causes mitochondrial damage in endothelium of rat cerebral blood vessels
- Decreases cell viability in bronchial epithelial cells
- Increases susceptibility of rat cerebral vascular endothelium to pathological stimuli