Methyl iodide
Itsura
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Mga pangalan | |
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Pangalang IUPAC
Iodomethane
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Mga ibang pangalan
Monoiodomethane, Methyl iodine, MeI, Halon 10001, UN 2644
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Mga pangkilala | |
Modelong 3D (JSmol)
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ChemSpider | |
Infocard ng ECHA | 100.000.745 |
Bilang ng EC |
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KEGG | |
PubChem CID
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Bilang ng RTECS |
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Dashboard ng CompTox (EPA)
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Mga pag-aaring katangian | |
CH3I | |
Bigat ng molar | 141.94 g/mol |
Hitsura | Malinaw na walang kulay na likido na may akridong amoy |
Densidad | 2.28 g/cm3 (20 °C)[1] |
Puntong natutunaw | −66.45 °C (−87.61 °F; 206.70 K) |
Puntong kumukulo | 42.43 °C (108.37 °F; 315.58 K) |
Solubilidad sa tubig
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1.4 g/100 mL (20 °C) |
log P | 1.51 |
Presyon ng singaw | 50 kPa at 20 °C 53.32 at 25.3 °C 166.1 kPa at 55 °C |
Repraktibong indeks (nD)
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1.531 |
Mga panganib | |
NFPA 704 (diyamanteng sunog) | |
Mga hangganan ng pagsabog | 8.5 - 66% |
Panimulang saklaw na halaga (TLV)
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2 ppm (TWA), 5 ppm (STEL) |
Nakakamatay na dosis o konsentrasyon (LD, LC): | |
LD50 (dosis na panggitna)
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0.78 mmol/kg (mouse, s.c.)[1] |
Maliban kung saan nabanggit, binigay ang datos para sa mga materyales sa kanilang estadong pamantayan (sa 25 °C [77 °F], 100 kPa).
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Ang Methyl iodide, tinatawag ding iodomethane, at kadalasang pinapaikli bilang "MeI", ay isang kompuwesto na may pormulang CH3I.
Talababa
[baguhin | baguhin ang wikitext]- ↑ 1.0 1.1 Merck Index, 11th Edition, 6002
Karagdagang Talababa
[baguhin | baguhin ang wikitext]- March, Jerry (1992), Advanced Organic Chemistry: Reactions, Mechanisms, and Structure (ika-4th (na) edisyon), New York: Wiley, ISBN 0-471-60180-2
{{citation}}
: CS1 maint: date auto-translated (link) - Sulikowski, G. A.; Sulikowski, M. M. (1999). in Coates, R.M.; Denmark, S. E. (Eds.) Handbook of Reagents for Organic Synthesis, Volume 1: Reagents, Auxiliaries and Catalysts for C-C Bond Formation New York: Wiley, pp. 423–26.
- Bolt H. M., Gansewendt B. (1993). "Mechanisms of carcinogenicity of methyl halides". Crit Rev Toxicol. 23 (3): 237–53. doi:10.3109/10408449309105011. PMID 8260067.
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Mga kawing panlabas
[baguhin | baguhin ang wikitext]- International Chemical Safety Card 0509
- NIOSH Pocket Guide to Chemical Hazards 0420
- IARC Summaries & Evaluations: Vol. 15 (1977), Vol. 41 (1986), Vol. 71 (1999)
- Metabolism of iodomethane in the rat
- Iodomethane NMR spectra Naka-arkibo 2007-02-10 sa Wayback Machine.
- Jones, Nicola (Setyembre 24, 2009). "Strawberry pesticide leaves sour taste: Methyl iodide use by Californian farmers up for review". Nature News. doi:10.1038/news.2009.943. Nakuha noong Setyembre 25, 2009.
{{cite journal}}
: CS1 maint: date auto-translated (link)
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- Articles without InChI source
- Articles without UNII source
- ECHA InfoCard ID from Wikidata
- Articles with changed KEGG identifier
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- Organoiodides
- Halomethanes
- Methylating agents
- IARC Group 3 carcinogens
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