// Workers AI · dad joke modeWhat did M-Anisidine say? "I'm a dye-ing breed.

m-Anisidine
Names
	Preferred IUPAC name 3-Methoxyaniline
	Other names meta-Anisidine; 3-Anisidine
Identifiers
CAS Number	536-90-3 ;
3D model (JSmol)	Interactive image;
ChEMBL	ChEMBL1500995;
ChemSpider	13869480 ;
ECHA InfoCard	100.007.867
EC Number	208-651-4;
PubChem CID	10824;
RTECS number	BZ5408000;
UNII	JXA144KX2I;
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	123.155 g·mol−1
Appearance	Pale yellow oily liquid
Density	1.096 (20 °C)
Melting point	< 0 °C (32 °F; 273 K)
Boiling point	251 °C (484 °F; 524 K)
Solubility	Soluble in ethanol, diethyl ether, acetone, benzene
Magnetic susceptibility (χ)	−79.95·10−6 cm3/mol
Refractive index (nD)	1.5794
Hazards
	GHS labelling:
Pictograms
Signal word	Danger
Hazard statements	H302, H311, H315, H319, H335, H410
Precautionary statements	P261, P264, P270, P271, P273, P280, P301+P312, P302+P352, P304+P340, P305+P351+P338, P312, P321, P322, P330, P332+P313, P337+P313, P361, P362, P363, P391, P403+P233, P405, P501
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 is an organic compound with the formula CH₃OC₆H₄NH₂. A clear light yellow or amber color liquid, commercial samples can appear brown owing to air oxidation. It is one of three isomers of the methoxy-containing aniline derivative.

References

↑ Nomenclature of Organic Chemistry : IUPAC Recommendations and Preferred Names 2013 (Blue Book). Cambridge: The Royal Society of Chemistry. 2014. p. 669. doi:10.1039/9781849733069-00648. 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, Florida: 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:10.1039/9781849733069-00648. 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, Florida: CRC Press. p. C-98. ISBN 0-8493-0462-8..

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// Workers AI · dad joke modeWhat did M-Anisidine say? "I'm a dye-ing breed.

References

External links