1,4-Dicyanobenzene

1,4-Dicyanobenzene
Names
	Other names Terephthalonitrile; p-Dicyanobenzene
Identifiers
CAS Number	623-26-7;
3D model (JSmol)	Interactive image;
ChEMBL	ChEMBL3248224;
ChemSpider	11672;
ECHA InfoCard	100.009.804
EC Number	210-783-2;
PubChem CID	12172;
UNII	E6ITH5CIS3;
CompTox Dashboard (EPA)	DTXSID1060768;
	InChI InChI=1S/C8H4N2/c9-5-7-1-2-8(6-10)4-3-7/h1-4H Key: BHXFKXOIODIUJO-UHFFFAOYSA-N;
	SMILES C1=CC(=CC=C1C#N)C#N;
Properties
Chemical formula	C8H4N2
Molar mass	128.134 g·mol−1
Appearance	white solid
Melting point	224–227 °C (435–441 °F; 497–500 K)
Hazards
GHS pictograms
GHS Signal word	Warning
GHS hazard statements	H315, H319, H335
GHS precautionary statements	P261, P264, P271, P280, P302+352, P304+340, P305+351+338, P312, P321, P332+313, P337+313, P362, P403+233, P405, P501
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
	Infobox references

1,4-Dicyanobenzene is an organic compound with the formula C₆H₄(CN)₂. Two other isomers exist, phthalonitrile and isophthalonitrile. All three isomers are produced commercially by ammoxidation of the corresponding xylene isomers. 1,4-Dicyanobenzene is a colorless or white solid with low solubility in water.[1] Hydrogenation of isophthalonitrile affords p-xylylenediamine.

Safety

LD50 (rat, oral) is 6400 mg/kg.

gollark: ↑

gollark: That's really bad as an argument! I explained this!

gollark: Lots of things are!

gollark: Well, yes.

gollark: Or via a bodily autonomy argument.

References

Pollak, Peter; Romeder, Gérard; Hagedorn, Ferdinand; Gelbke, Heinz-Peter (2000). "Nitriles". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a17_363.

This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.

[1] Pollak, Peter; Romeder, Gérard; Hagedorn, Ferdinand; Gelbke, Heinz-Peter (2000). "Nitriles". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a17_363.