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t is an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dyestuffs. The reducing properties of 1,5-diaminonaphthalene (1,5-DAN) as a MALDI matrix ( matrix-assisted laser desorption ionization) to amino acid sequencing and disulfide bond mapping of human urotensin II possessing one disulfide bond, and human guanylin possessing two disulfide bonds.
Yuko Fukuyama.;Shinichi Iwamoto.; Koichi Tanaka. Rapid sequencing and disulfide mapping of peptides containing disulfide bonds by using 1,5-diaminonaphthalene as a reductive matrix. Journal of Mass Spectrometry. 2006, 41 (2),191-201 .
Minh-Chau Pham.; Mohamed Oulahyne.; Malik Mostefai.; Mohamed Mehdi Chehimi. Multiple internal reflection FT-IR spectroscopy (MIRFTIRS) study of the electrochemical synthesis and redox process of poly (1,5-diaminonaphthalene). Synth. Met. 1998, 93 (2),89-96 .
Hazard Statements: H351
Suspected of causing cancer.
Precautionary Statements: P201-P280-P202-P308+P313-P405-P501a
Obtain special instructions before use. Wear protective gloves/protective clothing/eye protection/face protection. Do not handle until all safety precautions have been read and understood. IF exposed or concerned: Get medical advice/attention. Store locked up. Dispose of contents/container in accordance with local/regional/national/international regulations.