5 Results for "

primary aromatic amines

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

5 Results for "primary aromatic amines" in MCE Product Catalog:

1
1 Cited Publications
Referencia número: HY-W016729
No. CAS: 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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Referencia número: HY-D0017
No. CAS: 605-65-2
Synonyms: DNSCl
Dansyl chloride is a reagent that produces stable blue or blue-green fluorescent sulfonamide adducts in the reaction of aliphatic and aromatic amines with primary amino groups, and is widely used for modified amino acids, protein sequencing and amino acid analysis .
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Referencia número: HY-D0017S
No. CAS: 1276379-68-0
Synonyms: DNSCl-d6
Dansyl chloride-d6 is the deuterium labeled Dansyl chloride (HY-D0017). Dansyl chloride is a reagent that produces stable blue or blue-green fluorescent sulfonamide adducts in the reaction of aliphatic and aromatic amines with primary amino groups, and is widely used for modified amino acids, protein sequencing and amino acid analysis .
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Referencia número: HY-W354693
No. CAS: 615-05-4
Áreas de investigación:  

Others

2,4-Diaminoanisole is a carcinogenic aromatic primary amine compound that can be used in the analysis of reference standards .
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Referencia número: HY-D0017S1
No. CAS: 274250-28-1
Synonyms: DNSCl-13C2
Dansyl chloride- 13C2 is the 13C labeled Dansyl chloride (HY-D0017) . Dansyl chloride is a reagent that produces stable blue or blue-green fluorescent sulfonamide adducts in the reaction of aliphatic and aromatic amines with primary amino groups, and is widely used for modified amino acids, protein sequencing and amino acid analysis.
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