70800
1-萘胺-5-磺酸
technical, ≥60.0% (T)
别名:
5-氨基-1-萘磺酸, Laurent 酸
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关于此项目
经验公式（希尔记法）:
C10H9NO3S
化学文摘社编号:
分子量:
223.25
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
201-571-0
Beilstein/REAXYS Number:
2214149
MDL number:
产品名称
1-萘胺-5-磺酸, technical, ≥60.0% (T)
InChI key
DQNAQOYOSRJXFZ-UHFFFAOYSA-N
InChI
1S/C10H9NO3S/c11-9-5-1-4-8-7(9)3-2-6-10(8)15(12,13)14/h1-6H,11H2,(H,12,13,14)
SMILES string
Nc1cccc2c(cccc12)S(O)(=O)=O
grade
technical
form
powder
concentration
≥60.0% (T)
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signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Dermal - Skin Corr. 1B
存储类别
8B - Non-combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
法规信息
新产品
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Y T Kim et al.
The Journal of biological chemistry, 263(27), 13712-13717 (1988-09-25)
Physical interactions between pyridoxal kinase and aspartate aminotransferase were detected by means of emission anisotropy and affinity chromatography techniques. Binding of aspartate aminotransferase (apoenzymes) to pyridoxal kinase tagged with a fluorescent probe was detected by emission anisotropy measurements at pH
U Bhattacharyya et al.
The Journal of biological chemistry, 274(21), 14573-14578 (1999-05-18)
In the previous paper we demonstrated that uridine-5'-beta-1-(5-sulfonic acid) naphthylamidate (UDPAmNS) is a stacked and quenched fluorophore that shows severalfold enhancement of fluorescence in a stretched conformation. UDPAmNS was found to be a powerful competitive inhibitor (Ki = 0.2 mM)
Yuta Takigawa et al.
Chemical & pharmaceutical bulletin, 68(3), 258-264 (2020-03-03)
Oxo-octadecadienoic acids (OxoODEs) act as peroxisome proliferator-activated receptor (PPAR) agonists biologically, and are known to be produced in the lipoxygenase/linoleate system. OxoODEs seem to originate from the linoleate alkoxyl radicals that are generated from (E/Z)-hydroperoxy octadecadienoic acids ((E/Z)-HpODEs) by a
V Gianotti et al.
Chemosphere, 67(10), 1993-1999 (2007-01-26)
HPLC-DAD, HPLC-MS/MS, GC-MS and spectrophotometric methods are employed to investigate the degradation process of sodium 1-amino-5-naphthalene sulfonate (1A5NS) aqueous solutions, when exposed to sunlight and UV-lamp (254 nm) irradiations. Experimental results show that both sunlight and 254 nm UV-lamp irradiations
S C Tyagi et al.
The Journal of biological chemistry, 262(22), 10684-10688 (1987-08-05)
New fluorescent derivatives of dinucleoside monophosphates, (5'-AmNS)UpA/ApU/GpU/CpA, with a fluorophore, 1-aminonaphthalene-5-sulfonic acid (AmNS), attached to the first nucleotide of the dinucleoside monophosphates via a 5'-secondary amine linkage were synthesized in good yield. The chemical structure of (5'-AmNS)ApU was proved by
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