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Sodium anthraquinone-1-sulfonate

Sodium anthraquinone-1-sulfonate structure

Sodium anthraquinone-1-sulfonate 

structure
  • CAS No:

    128-56-3

  • Formula:

    C14H8O5S.Na

  • Chemical Name:

    Sodium anthraquinone-1-sulfonate

  • Synonyms:

    1-Anthracenesulfonic acid,9,10-dihydro-9,10-dioxo-,sodium salt (1:1);1-Anthracenesulfonic acid,9,10-dihydro-9,10-dioxo-,sodium salt;9,10-Anthraquinone-1-sulfonate sodium salt;Golden Salt;Gold Salt;Sodium anthraquinone-1-sulfonate;Sodium anthraquinone-α-sulfonate;1-Anthraquinonesulfonic acid sodium salt

  • Categories:

    Chemical Reagents  >  Organic Reagents

Sodium anthraquinone-1-sulfonate Basic Attributes

310.26

309.991180

204-894-5

29143990

Characteristics

99.72000

2.44690

cream to yellow crystalline powder.

1.585g/cm3

0ºC ( 32.00ºCF)

H2O: MODERATELY soluble

Anthraquinonesulfonic acids are strong acids which are readily soluble in water. /Anthraquinonesulfonic acids/

Safety Information

24/25

CB1095540

SRP: At the time of review, criteria for land treatment or burial (sanitary landfill) disposal practices are subject to significant revision. Prior to implementing land disposal of waste residue (including waste sludge), consult with environmental regulatory agencies for guidance on acceptable disposal practices.

Drug Information

Quinones (ie, 6,12-dione) have been shown to undergo oxidation-reduction cycles involving quinone, hydroquinone, and molecular oxygen, resulting in the formation of oxygen radicals and semiquinone radicals. /Quinones/

Chronic neurotoxic effects include vision disturbances. /From table; Quinones/

Sodium anthraquinone-1-sulfonate Use and Manufacturing

Methods of Manufacturing

K salt, also called diamant salt, is prepared by sulfonation in the presence of, eg, 0.5% mercury in 20% oleum, an amount of SO3 adequate for the sulfonation of about 60% of the charge. The reaction is controlled in such a manner that about 50% of the anthraquinone remains unsulfonated. After mercury is precipitated as the sulfide, the unreacted anthraquinone is precipitated by dilution and is collected by filtration. After washing and drying, it is recirculated as "reclaimed quinone". Mercury is removed completely from the filtrate, and the anthraquinone-1-sulfonic acid is then precipitated as the potassium salt. /Anthraquinone-1-sulfonic acid, potassium salt/|Sodium salt, also called silver salt, is prepared by sulfonation of anthraquinone in the absence of mercury. The acid also can be obtained from the 1,6- (or 1,7-) disulfonic acid by desulfonation at the alpha position in dilute sulfuric acid. /Anthraquinone-2-sulfonic acid, sodium salt/

Uses

Used as dye intermediate

1-Anthracenesulfonic acid, 9,10-dihydro-9,10-dioxo-, sodium salt (1:1): ACTIVE

Computed Properties

Molecular Weight:310.26
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:1
Exact Mass:309.99118878
Monoisotopic Mass:309.99118878
Topological Polar Surface Area:99.7
Heavy Atom Count:21
Complexity:538
Covalently-Bonded Unit Count:2
Compound Is Canonicalized:Yes

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