Monosodium acetylide
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IUPAC name Ethynylsodium | |
Other names sodium acetylide, sodium ethynide | |
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ChEBI |
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ChemSpider |
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ECHA InfoCard | 100.012.645 |
EC Number |
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Gmelin Reference | 174471 |
PubChem CID |
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CompTox Dashboard (EPA) |
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InChI
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Properties | |
Chemical formula | C2HNa |
Molar mass | 48.020 g·mol−1 |
Appearance | white solid |
Density | 1.352 g/cm3 |
Solubility in water | hydrolysis |
Hazards | |
GHS labelling:[1] | |
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Danger | |
Hazard statements | H261, H314 |
Precautionary statements | P231+P232, P260, P264, P280, P301+P330+P331, P302+P361+P354, P304+P340, P305+P354+P338, P316, P321, P363, P370+P378, P402+P404, P405, P501 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references |
Chemical compound
Monosodium acetylide is an organosodium compound with the formula NaC2H. It is a derived from acetylene by deprotonation using a sodium base, typically sodium amide.[2] This compound, a white solid, has been characterized by neutron diffraction, which revealed an Na-C bond and an elongated C≡C bond of 1.27 Å, which is longer than the C≡C bond length in acetylene itself (1.204 Å).[3] As a reagent, monosodium acetylide has been largely displaced by monolithium acetylide, which can be prepared more easily.[4]
References
- ^ "Sodium acetylide". pubchem.ncbi.nlm.nih.gov. Retrieved 3 September 2023.
- ^ K. N. Campbell, B. K. Campbell (1950). "n-Butylacetylene". Organic Syntheses. 30: 15. doi:10.15227/orgsyn.030.0015.
- ^ Atoji, Masao (1972). "Neutron Structure Determination of Monosodium Acetylide, NaC2H, at 293 and 5K". The Journal of Chemical Physics. 56 (10): 4947–4951. Bibcode:1972JChPh..56.4947A. doi:10.1063/1.1676972.
- ^ M. M. Midland; J. I. McLoughlin; R. T. Werley Jr. (1990). "Preparation and Use of Lithium Acetylide: 1-Methyl-2-Ethynyl-endo-3,3-Dimethyl-2-Norbornanol". Organic Syntheses. 68: 14. doi:10.15227/orgsyn.068.0014.