Dithiooxamide

Dithiooxamide
Names
	Preferred IUPAC name Ethanedithioamide
	Other names dithiooxamide, rubeanic acid
Identifiers
CAS Number	79-40-3 ;
3D model (JSmol)	Interactive image;
ChemSpider	2058248 ;
ECHA InfoCard	100.001.095
PubChem CID	2777982;
UNII	HE28T8Z08D ;
CompTox Dashboard (EPA)	DTXSID3020546 ;
	InChI InChI=1S/C2H4N2S2/c3-1(5)2(4)6/h(H2,3,5)(H2,4,6) Key: OAEGRYMCJYIXQT-UHFFFAOYSA-N ; InChI=1/C2H4N2S2/c3-1(5)2(4)6/h(H2,3,5)(H2,4,6) Key: OAEGRYMCJYIXQT-UHFFFAOYAT;
	SMILES S=C(N)C(=S)N;
Properties
Chemical formula	C2H4N2S2
Molar mass	120.19 g·mol−1
Hazards
	GHS labelling:
Pictograms
Signal word	Warning
Hazard statements	H302, H315, H319, H335
Precautionary statements	P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P340, P305+P351+P338, P312, P321, P330, P332+P313, P337+P313, P362, P403+P233, P405, P501
Safety data sheet (SDS)	External MSDS
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). verify (what is ?) Infobox references

Dithiooxamide, also known as rubeanic acid, is an organic compound. It is the sulfur analog of oxamide. It acts as a chelating agent, e.g. in the detection or determination of copper.^[2]^[3] It has also been used as a building block in the synthesis of cyclen.^[4]

References[edit]

^ GHS: PubChem
^ "Stainsfile - Howell's rubeanic acid for copper". stainsfile.info. Archived from the original on 2006-02-13.
^ "Strengthen science. Advance justice".
^ David P. Reed and Gary R. Weisman (2004). "1,4,7,10-Tetraazacyclododecane". Organic Syntheses; Collected Volumes, vol. 10, p. 667.

This article about an organic compound is a stub. You can help Wikipedia by expanding it.

[1] GHS: PubChem

[2] "Stainsfile - Howell's rubeanic acid for copper". stainsfile.info. Archived from the original on 2006-02-13.

[3] "Strengthen science. Advance justice".

[4] David P. Reed and Gary R. Weisman (2004). "1,4,7,10-Tetraazacyclododecane". Organic Syntheses; Collected Volumes, vol. 10, p. 667.

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