m-Anisidine

m-Anisidine
Names
	Preferred IUPAC name 3-Methoxyaniline
	Other names m-Anisidine (no longer recommended)
Identifiers
CAS Number	536-90-3 ;
3D model (JSmol)	Interactive image;
ChemSpider	13869480 ;
ECHA InfoCard	100.007.867
EC Number	208-651-4;
UN number	2431
CompTox Dashboard (EPA)	DTXSID8024529 ;
	InChI InChI=1S/C7H9NO/c1-9-7-4-2-3-6(8)5-7/h2-5H,8H2,1H3 Key: NCBZRJODKRCREW-UHFFFAOYSA-N ; InChI=1/C7H9NO/c1-9-7-4-2-3-6(8)5-7/h2-5H,8H2,1H3;
	SMILES Nc1cccc(OC)c1;
Properties
Chemical formula	C7H9NO
Molar mass	123.15 g/mol
Appearance	pale yellow oily liquid
Density	1.096 (20 °C), liquid
Melting point	< 0 °C (32 °F; 273 K)
Boiling point	251 °C (484 °F; 524 K)
Solubility	soluble in ethanol, diethyl ether, acetone, benzene
Refractive index (nD)	1.5794
Hazards
Flash point	> 122 °C (252 °F; 395 K)
Autoignition; temperature	515 °C (959 °F; 788 K)
Related compounds
Related compounds	o-Anisidine; p-Anisidine
	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

m-Anisidine one of the three isomers of anisidine. It is very poisonous for the blood leading to pink coloration of the skin and inner suffocation. Additionally its vapors are irritating to eyes, mucous membranes, the respiratory system and skin.

References

^ Nomenclature of Organic Chemistry : IUPAC Recommendations and Preferred Names 2013 (Blue Book). Cambridge: The Royal Society of Chemistry. 2014. p. 669. doi:10.1039/9781849733069-FP001. ISBN 978-0-85404-182-4. The names 'toluidine', 'anisidine', and 'phenetidine' for which o-, m-, and p- have been used to distinguish isomers, and 'xylidine' for which numerical locants, such as 2,3-, have been used, are no longer recommended, nor are the corresponding prefixes 'toluidine', 'anisidino', 'phenetidine', and 'xylidino'.
^ Weast, Robert C., ed. (1981). CRC Handbook of Chemistry and Physics (62nd ed.). Boca Raton, FL: CRC Press. p. C-98. ISBN 0-8493-0462-8..

External links

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[iupac2013-1] Nomenclature of Organic Chemistry : IUPAC Recommendations and Preferred Names 2013 (Blue Book). Cambridge: The Royal Society of Chemistry. 2014. p. 669. doi:10.1039/9781849733069-FP001. ISBN 978-0-85404-182-4. The names 'toluidine', 'anisidine', and 'phenetidine' for which o-, m-, and p- have been used to distinguish isomers, and 'xylidine' for which numerical locants, such as 2,3-, have been used, are no longer recommended, nor are the corresponding prefixes 'toluidine', 'anisidino', 'phenetidine', and 'xylidino'.

[2] Weast, Robert C., ed. (1981). CRC Handbook of Chemistry and Physics (62nd ed.). Boca Raton, FL: CRC Press. p. C-98. ISBN 0-8493-0462-8..

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