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Key Documents

250899

Sigma-Aldrich

1,5-Naphthalenedisulfonic acid disodium salt hydrate

95%

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About This Item

Linear Formula:
C10H6(SO3Na)2 · xH2O
CAS Number:
Molecular Weight:
332.26 (anhydrous basis)
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

95%

form

powder

SMILES string

[Na+].[Na+].[O-]S(=O)(=O)c1cccc2c(cccc12)S([O-])(=O)=O

InChI

1S/C10H8O6S2.2Na/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);;/q;2*+1/p-2

InChI key

YGSZNSDQUQYJCY-UHFFFAOYSA-L

General description

The liposomal entrapment of 1,5-naphthalenedisulfonic acid disodium salt in phospholipid vesicles has been studied. Doubly substituted aromatic dianions of 1,5-naphthalenedisulfonic acid disodium salt has been investigated by collision-induced dissociation, along with infrared multiple photon dissociation/detachment techniques.

Other Notes

Contains sodium chloride

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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H C Chang et al.
Journal of pharmaceutical sciences, 83(7), 1043-1046 (1994-07-01)
The liposomal entrapment of suramin and similar compounds in phospholipid vesicles was examined. For dipalmitoylphosphatidylcholine (DPPC) liposomes, entrapment percentages ranged from 25 to 65% with 3-25 mM phospholipid for aqueous solutions containing 0.07 mM of suramin. Incorporation of 30-50 mol
Shaun Ard et al.
The Journal of chemical physics, 132(9), 094301-094301 (2010-03-10)
Collision-induced dissociation (CID), along with infrared multiple photon dissociation/detachment (IRMPD) techniques, is utilized to study a series of doubly substituted aromatic dianions containing sulfonate and carboxylate functionalities (1,2- and 1,3-benzenedisulfonate, 1,5-naphthalenedisulfonate, 2,6-naphthalenedisulfonate, 4-sulfobenzoate, 2,6-naphthalenedicarboxylate, and terephthalate dianions). The molecules were

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