Chemistry:2,4-Xylidine
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Names | |
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Preferred IUPAC name
2,4-Dimethylaniline | |
Other names
2,4-Dimethylphenylamine
2,4-Dimethylbenzenamine | |
Identifiers | |
3D model (JSmol)
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636243 | |
ChEBI | |
ChEMBL | |
ChemSpider | |
EC Number |
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KEGG | |
PubChem CID
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RTECS number |
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UNII | |
UN number | 1711 |
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Properties | |
C8H11N | |
Appearance | colourless liquid |
Density | 0.9763 |
Melting point | −15.9 °C (3.4 °F; 257.2 K) |
Boiling point | 218.0 °C (424.4 °F; 491.1 K) |
low | |
Hazards | |
GHS pictograms | |
GHS Signal word | Warning |
H301, H311, H319, H330, H331, H373, H411 | |
P260, P261, P264, P270, P271, P273, P280, P284, P301+310, P302+352, P304+340, P305+351+338, P310, P311, P312, P314, P320, P321, P322, P330, P337+313, P361, P363, P391, P403+233 | |
Flash point | 100 |
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 | |
Tracking categories (test):
2,4-Xylidine is an organic compound with the formula C6H3(CH3)2NH2. It is one of several isomeric xylidines. It is a colorless viscous liquid. Commercially significant derivatives include the veterinary drug cymiazole and the colorant Pigment Yellow 81.[1]
It is prepared by nitration of m-xylene followed by hydrogenation.
References
- ↑ Meyer, M. (2012). "Xylidines". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a28_455. ISBN 978-3527306732.
Original source: https://en.wikipedia.org/wiki/2,4-Xylidine.
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