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7-AMINO-1,3-NAPHTHALENEDISULFONIC ACID MONOPOTASSIUM SALT

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7-AMINO-1,3-NAPHTHALENEDISULFONIC ACID MONOPOTASSIUM SALT Basic information

Product Name:
7-AMINO-1,3-NAPHTHALENEDISULFONIC ACID MONOPOTASSIUM SALT
Synonyms:
  • 3-naphthalenedisulfonicacid,7-amino-monopotassiumsalt
  • ANDS, POTASSIUM SALT
  • 7-AMINO-1,3-NAPHTHALENEDISULFONIC ACID MONOPOTASSIUM SALT
  • 7-AMINONAPHTHALENE-1,3-DISULFONIC ACID, POTASSIUM SALT
  • 2-NAPHTHYLAMINE-6,8-DISULFONIC ACID MONOPOTASSIUM SALT
  • potassium hydrogen 7-aminonaphthalene-1,3-disulphonate
  • amino G acid,2-naphthyl-amine-6,8-disulfonic acid
  • 7-Amino-1,3-naphthalenedisulfonic acid monopotassium salt monohydrate
CAS:
842-15-9
MF:
C10H10KNO6S2
MW:
343.41
EINECS:
212-669-8
Product Categories:
  • Intermediates of Dyes and Pigments
Mol File:
842-15-9.mol
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7-AMINO-1,3-NAPHTHALENEDISULFONIC ACID MONOPOTASSIUM SALT Chemical Properties

form 
powder to crystal
color 
White to Orange to Green
InChI
InChI=1S/C10H9NO6S2.K.H/c11-7-2-1-6-3-8(18(12,13)14)5-10(9(6)4-7)19(15,16)17;;/h1-5H,11H2,(H,12,13,14)(H,15,16,17);;
InChIKey
GOPRYBNRWIBTIH-UHFFFAOYSA-M
SMILES
S(C1=CC(S(O)(=O)=O)=CC2C=CC(N)=CC1=2)(O)(=O)=O.[KH]
LogP
-0.314 (est)
CAS DataBase Reference
842-15-9(CAS DataBase Reference)
EPA Substance Registry System
1,3-Naphthalenedisulfonic acid, 7-amino-, monopotassium salt (842-15-9)
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Safety Information

Safety Statements 
22-24/25
WGK Germany 
3
HS Code 
2921.45.1000
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7-AMINO-1,3-NAPHTHALENEDISULFONIC ACID MONOPOTASSIUM SALT Usage And Synthesis

Description

7-Amino-1,3-naphthalenedisulfonic acid monopotassium salt monohydrate is a fluorescent label for carbohydrates.

Uses

7-Amino-1,3-naphthalenedisulfonic Acid Monopotassium Salt Monohydrate is a fluorescent label for carbohydrates. It can be used as analyte in analytical study of microplate-based detection of lytic polysaccharide monooxygenase activity by fluorescence-labeling of insoluable oxidized products.

Uses

To label carbohydrates, this fluorescent reagent reacts with the reducing termini of oligosaccharids to form a Schiffs base, which can then be stabilized by reducing it with sodium cyanoborohydride.

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