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Dithiosalicylic acid, also known as 2,3-dihydroxy-1,4-dithiacyclohexane-6,6-dione, is an organic compound with the chemical formula C6H6O4S2. It is a white crystalline solid that is soluble in water and has a molecular weight of 218.24 g/mol. Dithiosalicylic acid is a chelating agent, which means it can form stable complexes with metal ions, particularly those of transition metals. This property makes it useful in various applications, such as in analytical chemistry for the determination of metal ions, in the synthesis of metal complexes, and in the removal of heavy metals from industrial waste streams. The compound is also known for its ability to reduce disulfide bonds in proteins, which can be useful in biochemical research and in the preparation of certain pharmaceuticals.

527-89-9

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527-89-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 527-89-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,2 and 7 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 527-89:
(5*5)+(4*2)+(3*7)+(2*8)+(1*9)=79
79 % 10 = 9
So 527-89-9 is a valid CAS Registry Number.

527-89-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name dithiosalicylic acid

1.2 Other means of identification

Product number -
Other names 6-[bis(sulfanyl)methylidene]cyclohexa-2,4-dien-1-one

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:527-89-9 SDS

527-89-9Relevant academic research and scientific papers

Synthesis, characterization and antitumor studies of Mn(II), Fe(III), Co(II), Ni(II), Cu(II) and Zn(II) complexes of N-salicyloyl-N′-o-hydroxythiobenzhydrazide

Shrivastav, Anuraag,Singh, Nand K.,Singh, Sukh Mahendra

, p. 887 - 895 (2002)

A new ligand N-salicyloyl-N′-o-hydroxythiobenzhydrazide (H2Sotbh) forms complexes [Mn(HSotbh)2], [Fe(Sotbh-H)(H2O)2], [M(Scotbh)] [M = Co(II), Cu(II) and Zn(II)] and [Ni(Sotbh)(H2O)2], which were characterized by various physico-chemical techniques. Moessbauer spectrum of [Fe(Sotbh-H)(H2O)2] reveals the quantum admixture of 5/2 and 3/2 spin-states. Mn(II), Cu(II) and Ni(II) complexes showed reversal of tumor bearing mice. Tumor bearing mice administered with Mn(II), Cu(II) and Ni(II) complexes showed reversal of tumor growth associated induction of apoptosis in lymphocytes. The paper discusses the possible mechanisms and therapeutic implications of the H2Sotbh and its metal complexes in tumor regression and the tumor growth associated immunosuppression. Copyright

Visible light assisted photodegradation of thimerosal by high performance ZnFe2O4/poly(o-phenylenediamine) composite

Sandoval, Claudio,Ranganathan, Suresh,Ramírez, Eimmy,Mansilla, Héctor D.,Dinamarca, Robinson,Pecchi, Gina,Yá?ez, Jorge

, p. 8 - 15 (2019/04/13)

Thimerosal is a mercury-based preservative that is used in pharmaceuticals, vaccines and health-care products. However, thimerosal toxicity has been well explored and hence it should be properly treated for avoiding its occurrence in the environment. Hence, we synthesized visible light active ZnFe2O4/poly(o-phenylenediamine) composite as photocatalyst for degradation of thimerosal. The well characterized ZnFe2O4 and composite effectively degraded thimerosal and subsequently reduced Hg(II) into Hg(0) under visible light irradiation. Thimerosal degradation by-products and generation of Hg(0) were analyzed by high performance liquid chromatography and atomic fluorescence spectroscopy. The composite showed better photocatalytic activity than the pure ZnFe2O4 nanoparticles. Under the optimum conditions, 90.2% degradation of thimerosal was achieved within 6 h of irradiation. An efficient charge separation ability of poly(o-phenylenediamine) contributes to the high photocatalytic performance of the composite. This work provides a new photocatalytic degradation pathway of thimerosal and thus will stimulate further studies in the removal of organometallic contaminants.

Pesticidal compositions containing phosphoric esters and divalent sulphur compounds

-

, (2008/06/13)

Pesticidal composition comprising: a pesticidal, phosphoric ester the molecule of which has at least one alkyl group of 1 to 3 carbon atoms, 0.05 to 10% of an agent stabilizing the said ester against decomposition by protonisation, together with adjuvants characterized in that the stabilizing agent comprises at least one sulphur compound containing per molecule at least one divalent sulphur atom of which one valence is bonded to an atom chosen from sulphur, carbon, nitrogen, hydrogen, and metals capable of giving a salt, the other valence being bonded to an atom chosen from hydrogen, the carbon atom already noted, a second carbon atom, the nitrogen atom already noted, a second nitrogen atom, the metal atom already noted in the case of a metal of valence greater than one, a second atom of metal and oxygen when the first valence is not attached to an atom of hydrogen, the proportion of sulphur calculated with reference to the weight of the sulphur compound being between 5 and 99%. Process for stabilizing a phosphoric ester of which the molecule possesses at least one alkyl group containing 1 to 3 carbon atoms characterized in that there is added to the phosphoric ester or to a mixture which contains it, 0.05 to 10% calculated on the weight of the phosphoric acid ester of an agent capable of stabilizing the said phosphoric ester against protonisation and comprising at least one sulphur compound such as that defined thereupon.

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