5 Results for "

Schiff base product

" in MedChemExpress (MCE) Product Catalog:
Products (5)

5 Results for "Schiff base product" in MCE Product Catalog:

1
4-(Dimethylamino)cinnamaldehyde
4-(Dimethylamino)cinnamaldehyde
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1 Cited Publications
Cat. No.: HY-W016729
CAS No.: 6203-18-5
4-(Dimethylamino) cinnamaldehyde is a staining agent that reacts with flavan-3-ols and Proanthocyanidins (HY-N0794) bearing meta-dihydroxyl or trihydroxyl phenol structures to form a green chromophore. In acidic media, 4-(Dimethylamino) cinnamaldehyde undergoes a condensation reaction with aromatic primary amines to produce colored and stable quinoid protonated Schiff base salts. 4-(Dimethylamino) cinnamaldehyde can be used to determine indole products of apotryptophanase and tryptophanase, as well as for the detection and analysis of Proanthocyanidins, with the absorbance detection wavelength of the calibration curve set at 640 nm .
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BODIPY FL hydrazide
BODIPY FL hydrazide
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Cat. No.: HY-114351
CAS No.: 178388-71-1
Purity:  97.40%
BODIPY FL Hydrazide is a green-fluorescent dye, BODIPY FL Hydrazide is reactive with aldehyde/ketone on polysaccharides and glycoproteins, yielding a reversible Schiff base product that can be transformed to a stable linkage using a reducing agent like sodium borohydride or sodium cyanoborohydride. (λex=495 nm, λem=516 nm) .
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BODIPY FL EDA free base
BODIPY FL EDA free base
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Cat. No.: HY-114346A
CAS No.: 220524-70-9
ODIPY FL EDA free base is an amine-based, green fluorescent probe. The R-NH2 of ODIPY FL EDA free base can be coupled with aldehydes or ketones to form reversible Schiff base products. Convert to stable amine derivatives using reducing agents such as sodium borohydride or sodium cyanoborohydride. ODIPY FL EDA free base can be used to detect modified or normal deoxynucleotides and demonstrate DNA damage and genomic DNA methylation.
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2,4-Dihydroxybenzaldehyde (Standard)
2,4-Dihydroxybenzaldehyde (Standard)
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Cat. No.: HY-W007539R
CAS No.: 95-01-2
Category:  

Monophenols Ketones, Aldehydes, Acids Phenols Polyphenols Endogenous metabolite

Target:  

Reference Standards Endogenous Metabolite Drug Intermediate NO Synthase Reactive Oxygen Species (ROS) COX

2,4-Dihydroxybenzaldehyde (Standard) is the analytical standard of 2,4-Dihydroxybenzaldehyde. This product is intended for research and analytical applications. 2,4-Dihydroxybenzaldehyde is an endogenous metabolite. 2,4-Dihydroxybenzaldehyde is a pharmaceutical intermediate that can be used to synthesize various Schiff base compounds. 2,4-Dihydroxybenzaldehyde exhibits significant anti angiogenic, anti-inflammatory, and analgesic activities. 2,4-Dihydroxybenzaldehyde reduces the production of NO and ROS by inhibiting the expression of iNOS and COX-2. 2,4-Dihydroxybenzaldehyde is commonly used in the study of inflammatory conditions .
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2-Naphthaldehyde (Standard)
2-Naphthaldehyde (Standard)
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Cat. No.: HY-Y0075R
CAS No.: 66-99-9
2-Naphthaldehyde (Standard) is the analytical standard of 2-Naphthaldehyde (HY-Y0075). This product is intended for research and analytical applications. 2-Naphthaldehyde is a naphthalene-based bi-aromatic aldehyde compound. 2-Naphthaldehyde scavenges DPPH and ABTS + free radicals, and exerts reductive effects by donating hydrogen atoms to terminate free radical chain reactions. 2-Naphthaldehyde inhibits the growth and proliferation of colon cancer cells. 2-Naphthaldehyde serves as a substrate for NAD +-dependent salicylaldehyde dehydrogenase from Pseudomonas strain C6 and is catalytically oxidized to 2-naphthoic acid. 2-Naphthaldehyde acts as a precursor material for the chemical synthesis of antioxidant Schiff bases .
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