Phenols
eMolecules 1293990-73-4 | O-PIVALOYLHYDROXYLAMINE TFOH | AstaTech267.220 | C6H12F3NO5S | 95.000 | CC(C)(C)C(=O)ON.OS(=O)(=O)C(F)(F)F | 25g | 881785783
O-PIVALOYLHYDROXYLAMINE TFOH | AstaTech | 1293990-73-4267.220 | C6H12F3NO5S | 95.000 | CC(C)(C)C(=O)ON.OS(=O)(=O)C(F)(F)F | 25g | 881785783
Medchemexpress LLC Cyclo(histidyl-proline) | 53109-32-3 | MFCD00133207 | 98.8% | 234.25 g/mol | C11H14N4O2 | 1 ML
Cyclo(histidyl-proline) is a cyclic dipeptide used in biochemical and cellular research to probe signaling pathways, including NF-κB-related inflammatory responses. The compound is provided as a ready-to-use 10 mM solution in water (1 mL) and is characterized by CAS 53109-32-3, formula C11H14N4O2, and molecular weight 234.25 g/mol.
- Ready-to-use 10 mM aqueous solution for immediate experiments.
- High purity for reproducible biochemical assays.
- Soluble in water and compatible with DMSO for assay flexibility.
- Well-characterized molecular identity for accurate compound tracking.
Medchemexpress LLC 7-chloro-3-methyl-3,4-dihydro-2H-1,2,4-benzothiadiazine 1,1-dioxide | 22503-72-6 | MFCD00270874 | 99.4% | 232.69 g/mol | C8H9ClN2O2S | 1 ML
IDRA-21 is a benzothiadiazine derivative that acts as a positive allosteric modulator of AMPA receptors. It inhibits AMPA receptor desensitization and is used in neuroscience research related to cognition, memory, and excitatory neurotransmission. The compound is supplied as a 10 mM solution in DMSO (1 mL) and is also available as solid quantities; reported purity is approximately 99.4%.
- Positive allosteric modulator of AMPA receptors.
- Inhibits AMPA receptor desensitization to enhance excitatory signaling.
- Useful for research on cognition and memory mechanisms.
- Available as a 10 mM solution in DMSO (1 mL) and in multiple solid sizes.
- High reported purity (~99.4%).
- Molecular weight 232.69 g/mol; formula C8H9ClN2O2S.
Aobchem 1-(3-Bromo-5-ethoxyphenyl)-2 2-dichloroethanol | 95% | CAS 2734778-80-2 | C10H11BrCl2O2 | 250mg
1-(3-Bromo-5-ethoxyphenyl)-2 2-dichloroethanol | 95% | CAS 2734778-80-2 | C10H11BrCl2O2 | 250mg
Aobchem 2-(4-Chlorophenyl)-N N-diethylacetamide | 95% | CAS 5292-72-8 | C12H16ClNO | 500mg
2-(4-Chlorophenyl)-N N-diethylacetamide | 95% | CAS 5292-72-8 | C12H16ClNO | 500mg
Aobchem 1-Bromo-2-methoxy-4-((4-methoxybenzyl)oxy)benzene | 97% | CAS 949019-87-8 | C15H15BrO3 | 500mg
1-Bromo-2-methoxy-4-((4-methoxybenzyl)oxy)benzene | 97% | CAS 949019-87-8 | C15H15BrO3 | 500mg
Aobchem 1-Bromo-4-(tert-butoxy)-2-methoxybenzene | 95% | CAS 1369870-90-5 | C11H15BrO2 | 250mg
1-Bromo-4-(tert-butoxy)-2-methoxybenzene | 95% | CAS 1369870-90-5 | C11H15BrO2 | 250mg
Aobchem Phenyl(3-propylphenyl)methanone | 95% | CAS 1644295-29-3 | C16H16O | 5g
Phenyl(3-propylphenyl)methanone | 95% | CAS 1644295-29-3 | C16H16O | 5g
Medchemexpress LLC Ribitol | 488-81-3 | MFCD00064291 | ≥98.0% | 152.15 g/mol | C5H12O5 | 25 G
Ribitol is a crystalline pentose alcohol used as an analytical reagent and metabolic pathway standard. It is commonly employed in biochemical research to study the pentose phosphate pathway and to serve as an endogenous metabolite or analytical standard. The compound is solid at room temperature and is routinely prepared into stock solutions for laboratory use.
- Crystalline pentose alcohol suitable for analytical use
- Used in metabolic pathway and endogenous metabolite studies
- Molecular formula C5H12O5; molecular weight 152.15 g/mol
- Supplied as a solid for preparation of stock solutions
- Storage guidance: powder stable at -20°C for years; in solvent store at -80°C for long-term
Medchemexpress LLC 1,3-bis(carboxyethoxy)-2,2-bis(carboxyethoxy)propane | 35638-19-8 | C17H28O12 | 10 G
1,3-bis(carboxyethoxy)-2,2-bis(carboxyethoxy)propane is a PEG-based PROTAC linker for synthesizing PROTACs. PROTACs use two ligands connected by a linker, one for an E3 ubiquitin ligase and another for a target protein, to exploit the intracellular ubiquitin-proteasome system for selective protein degradation. It is intended for research use only.
- PEG-based PROTAC linker
- Used in the synthesis of PROTACs
- Exploits the ubiquitin-proteasome system
- Selectively degrades target proteins
- For research use only