Adipamide

Adipamide
Names
	Preferred IUPAC name Adipamide
	Systematic IUPAC name Hexanediamide
	Other names Hexanedioic diamide
Identifiers
CAS Number	628-94-4 ;
3D model (JSmol)	Interactive image; Interactive image;
Beilstein Reference	4-02-00-01972
ChemSpider	11858 ;
ECHA InfoCard	100.010.057
EC Number	211-062-5;
MeSH	Adipamide
PubChem CID	12364;
RTECS number	AU7800000;
UNII	40DRU033OW ;
CompTox Dashboard (EPA)	DTXSID4020032 ;
	InChI InChI=1S/C6H12N2O2/c7-5(9)3-1-2-4-6(8)10/h1-4H2,(H2,7,9)(H2,8,10) Key: GVNWZKBFMFUVNX-UHFFFAOYSA-N ; InChI=1S/C6H12N2O2/c7-5(9)3-1-2-4-6(8)10/h1-4H2,(H2,7,9)(H2,8,10) Key: GVNWZKBFMFUVNX-UHFFFAOYSA-N; InChI=1/C6H12N2O2/c7-5(9)3-1-2-4-6(8)10/h1-4H2,(H2,7,9)(H2,8,10) Key: GVNWZKBFMFUVNX-UHFFFAOYAG;
	SMILES NC(=O)CCCCC(N)=O; O=C(N)CCCCC(=O)N;
Properties
Chemical formula	C6H12N2O2
Molar mass	144.174 g·mol−1
Appearance	powder
Melting point	220 to 225 °C (428 to 437 °F; 493 to 498 K)
Solubility in water	4.4 g/l (12 °C)
Related compounds
Related compounds	hexanedioic acid; hexanedihydrazide; hexanedioyl dichloride; hexanedinitrile
	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

Adipamide is the organic compound with the formula (CH₂CH₂C(O)NH₂)₂. It is a white solid. The dominant commercial interest in adipamides is related to their presence in nylons.

Adipamide is formed by treating dimethyl adipate with concentrated ammonia.^[1]^[2]

External links

MSDS at Oxford University

References

^ Musser, M. T. (2005). "Adipic Acid". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a01_269.
^ "Dimethyl Adipate". chemicalland21.com.

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

[Ullmann-1] Musser, M. T. (2005). "Adipic Acid". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a01_269.

[2] "Dimethyl Adipate". chemicalland21.com.

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