Weight | 269.753 g/mol |
---|---|
Formula | C12H12ClNO2S |
Hydrogen Acceptors | 3 |
Hydrogen Donors | 0 |
Aromatic Rings | 2 |
Rotatable Bonds | 2 |
Dansyl chloride (605-65-2)
5-(dimethylamino)naphthalene-1-sulfonylchloride · DNS-Cl · dansyl chloride, 3H-labeled
Score:
#2701 in Biochemistry
,
#6689 in Chemistry
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- [8] End-group analysis using dansyl chloride (Methods in Enzymology, 1972)
- [12] Dansyl chloride procedure (Methods in Enzymology, 1967)
- Derivatization of ethinylestradiol with dansyl chloride to enhance electrospray ionization: application in trace analysis of ethinylestradiol in rhesus monkey plasma. (Analytical Chemistry, 2002)
- [26a] Sequence analysis with dansyl chloride (Methods in Enzymology, 1972)
- Fluorimetric determination of oxidised and reduced glutathione in cells and tissues by high-performance liquid chromatography following derivatization with dansyl chloride (Journal of Chromatography B: Biomedical Sciences and Applications, 1991)
- Microanalysis of Amino Acids and Their Determination in Biological Material Using Dansyl Chloride (Biological Chemistry, 1972)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 5-(dimethylamino)naphthalene-1-sulfonylchloride
- DNS-Cl
- dansyl chloride, 3H-labeled
- 5-(N,N-dimethylamino)naphthalene-1-sulfonyl chloride
- dansylchloride
-
SMILESCN(C)C1=CC=CC2=C1C=CC=C2S(=O)(=O)Cl
-
InChIKeyXPDXVDYUQZHFPV-UHFFFAOYSA-N
- Pubchem - Dansyl chloride
- Wikipedia - dansyl chloride
Dansyl chloride or 5-(DimethylAmino)Naphthalene-1-SulfonYL chloride is a reagent that reacts with primary amino groups in both aliphatic and aromatic amines to produce stable blue- or blue-greenfluorescent sulfonamide adducts. It can also be made to react with secondary amines. Dansyl chloride is widely used to modify amino acids; specifically, protein sequencing and amino acid analysis.
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