Phenols
Boston Bioproducts Inc Bis-Acrylamide - 500ml
Bis-Acrylamide - 500ml (For Research Use and Further Manufacturing Only)
Medchemexpress LLC Rel-HDMP 28 hydrochloride | 219915-69-2 | 99.7% | 319.83 g/mol | C18H22ClNO2 | 1mg
rel-HDMP 28 hydrochloride (Compound 2g) is a methylphenidate analogue that binds selectively to SERT (Ki 105 nM)[1]
Medchemexpress LLC Pivaloyloxymethyl chloride | 18997-19-8 | MFCD00000884 | 100.0% | 150.60 g/mol | C6H11ClO2 | 100g
Pivaloyloxymethyl chloride is an intermediate Pivaloyloxymethyl chloride can be used in the synthesis of Compound 8b Compound 8b can stimulate the production of interferon gamma[1]
Medchemexpress LLC 3-hydroxyacetophenone | 121-71-1 | MFCD00002298 | >99.0% | 136.15 g/mol | C8H8O2 | 50g
3-Hydroxyacetophenone (m-Hydroxyacetophenone) is a hydroxy-substituted alkyl phenyl ketone and also a plant defensin in carnations 3-Hydroxyacetophenone has antifusarium activity In addition 3-Hydroxyacetophenone can be used to synthesize Rivastigmine (HY-17368)[1][2][3]
Chemscene ChemScene | 5-Fluoro-2-nitrophenol | 500G | CS-W008895 | 0.98 | 446-36-6| MFCD00007107 | 157.1
ChemScene | 5-Fluoro-2-nitrophenol | 500G | CS-W008895 | 0.98 | 446-36-6| MFCD00007107 | 157.1
Medchemexpress LLC Tris(hydroxymethyl)aminomethane | 77-86-1 | 99.9% | 500 G
THAM (Tris) is a biologically inert amino alcohol with low toxicity that buffers carbon dioxide and acids both in vitro and in vivo. It is an effective amine compound for pH control in the physiological range. It has been shown to reduce arterial carbon dioxide tension (PaCO2) levels and increase pH above 7.4 during infusion in pigs.
- Biologically inert amino alcohol with low toxicity
- Buffers carbon dioxide and acids
- Effective for pH control in the physiological range
- Reduces arterial carbon dioxide tension
- Increases pH during infusion
Medchemexpress LLC Bromo-PEG2-C2-azide | 530151-56-5 | 98.7% | 1 G
Bromo-PEG2-C2-azide is a versatile non-cleavable linker utilized in the synthesis of antibody-drug conjugates (ADCs) and as a PEG-based PROTAC linker for PROTAC synthesis. This click chemistry reagent contains an azide group, enabling its use in copper-catalyzed azide-alkyne cycloaddition (CuAAc) reactions with alkyne groups, as well as strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with DBCO or BCN groups.
- Non-cleavable ADC linker
- PEG-based PROTAC linker
- Contains an azide group for click chemistry
- Participates in copper-catalyzed azide-alkyne cycloaddition (CuAAc)
- Enables strain-promoted alkyne-azide cycloaddition (SPAAC)
- Useful in synthesis of antibody-drug conjugates (ADCs)
- Applicable in synthesis of PROTACs