39367
1-Dansylpiperazine
≥99.0%
Synonym(s):
1-[5-(Dimethylamino)naphthalene-1-sulfonyl]piperazine
Sign Into View Organizational & Contract Pricing
Select a Size
About This Item
Empirical Formula (Hill Notation):
C16H21N3O2S
CAS Number:
Molecular Weight:
319.42
MDL number:
UNSPSC Code:
41116105
PubChem Substance ID:
grade
derivatization grade ((HPLC))
Assay
≥99.0% (HPLC)
≥99.0%
mp
130-135 °C
fluorescence
λex 340 nm; λem 523 nm in methanol
SMILES string
CN(C)c1cccc2c(cccc12)S(=O)(=O)N3CCNCC3
InChI
1S/C16H21N3O2S/c1-18(2)15-7-3-6-14-13(15)5-4-8-16(14)22(20,21)19-11-9-17-10-12-19/h3-8,17H,9-12H2,1-2H3
InChI key
NRTFFCBHBQNURK-UHFFFAOYSA-N
Other Notes
Reagent for the fluorimetric determination of fatty acids in body fluids; fatty acids determination by pre-column derivatization
Signal Word
Warning
Hazard Statements
Hazard Classifications
Acute Tox. 4 Oral
Storage Class Code
13 - Non Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
新产品
This item has
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
I Yanagisawa et al.
Journal of chromatography, 345(2), 229-240 (1985-12-13)
The quantitative determination of saturated and unsaturated fatty acids (ranging from acetic acid to lignoceric acid) in biological samples is presented. The secondary amine group of 5-(dimethylamino)-1-naphthalenesulponyl-semipiperazide (dansyl-semipiperazide) reacts with the carboxyl group of the fatty acids to form an
A. Junker-Buchheit, H. Jork
Fresenius Journal of Analytical Chemistry, 331, 387-387 (1988)
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service