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1,5-Naphthalenedisulfonic acid tetrahydrate

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1,5-Naphthalenedisulfonic acid tetrahydrate Basic information

Product Name:
1,5-Naphthalenedisulfonic acid tetrahydrate
Synonyms:
  • 1,5-NAPHTHALENEDISULFONIC ACID TETRAHYDRATE
  • ARMSTRONG'S ACID
  • 1,5-Naphthalenedisulfonic acid tetrahydrate,Armstrong’s acid
  • 1,5-Naphthalenedisulfonic Acid 
  • 1,5-Naphthalenedisulfonic acid hydrate
  • 1,5-Disulphonaphthalene tetrahydrate, Armstrong's acid tetrahydrate
  • Naphthalene-1,5-disulphonic acid tetrahydrate
  • 1,5-Naphthalenedisulfonic acid tetrahydrate 97%
CAS:
211366-30-2
MF:
C10H10O7S2
MW:
306.3
EINECS:
678-302-2
Mol File:
211366-30-2.mol
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1,5-Naphthalenedisulfonic acid tetrahydrate Chemical Properties

storage temp. 
Sealed in dry,Room Temperature
Water Solubility 
Soluble in water
form 
powder to crystal
color 
White to Almost white
InChI
1S/C10H8O6S2.4H2O/c11-17(12,13)9-5-1-3-7-8(9)4-2-6-10(7)18(14,15)16;;;;/h1-6H,(H,11,12,13)(H,14,15,16);4*1H2
InChIKey
ZLBLYGIIADHDKG-UHFFFAOYSA-N
SMILES
O.O.O.O.OS(=O)(=O)c1cccc2c(cccc12)S(O)(=O)=O
CAS DataBase Reference
211366-30-2(CAS DataBase Reference)
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Safety Information

Hazard Codes 
C
Risk Statements 
34
Safety Statements 
26-36/37/39-45
RIDADR 
UN 2585 8/PG 3
WGK Germany 
3
HazardClass 
8
PackingGroup 
III
HS Code 
2904100090
Storage Class
8A - Combustible corrosive hazardous materials
Hazard Classifications
Eye Dam. 1
Skin Corr. 1B

MSDS

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1,5-Naphthalenedisulfonic acid tetrahydrate Usage And Synthesis

Chemical Properties

Gray powder crystal

Uses


  • Assessment of verapamil in a myotonic dystrophy model: Research demonstrated verapamil′s efficacy in mitigating chloride and calcium channel dysfunctions in a myotonic dystrophy mouse model, suggesting its potential in treating related muscular dystrophies (Cisco et al., 2024).

  • Cardiac tissue modeling with verapamil: Verapamil hydrochloride was tested using human-induced pluripotent stem cell-derived cardiac tissues to evaluate drug interactions and cardiac responses, proving essential for advancing cardiac safety pharmacology (Miyagawa et al., 2024).


General Description

1,5-Naphthalenedisulfonic acid tetrahydrate reacts with [n-Bu2SnO]n in a 1:1 stoichiometry followed by reaction with 2,2′-bipyridine-N,N′-dioxide (BPDO-I) to yield 1D-coordination polymer, [n-Bu2Sn(BPDO-I)(1,5-C10H6(SO3)2)]n.

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