Wikipedia

Methyl iodide

Ang Methyl iodide, tinatawag ding iodomethane, at kadalasang pinapaikli bilang "MeI", ay isang kompuwesto na may pormulang CH3I.

Methyl iodide
Mga pangalan
Pangalang IUPAC
Iodomethane
Mga ibang pangalan
Monoiodomethane, Methyl iodine, MeI, Halon 10001, UN 2644
Mga pangkilala
Modelong 3D (JSmol)
ChemSpider
Infocard ng ECHA 100.000.745 Baguhin ito sa Wikidata
Bilang ng EC
  • 200-819-5
KEGG
Bilang ng RTECS
  • PA9450000
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
 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)
 1.531
Mga panganib
NFPA 704 (diyamanteng sunog)
NFPA 704 four-colored diamondHealth 3: Short exposure could cause serious temporary or residual injury. E.g. chlorine gasFlammability 1: Must be pre-heated before ignition can occur. Flash point over 93 °C (200 °F). E.g. canola oilInstability 1: Normally stable, but can become unstable at elevated temperatures and pressures. E.g. calciumSpecial hazards (white): no code
3
1
1
Mga hangganan ng pagsabog 8.5 - 66%
Panimulang saklaw na halaga (TLV)
 2 ppm (TWA), 5 ppm (STEL)
Nakakamatay na dosis o konsentrasyon (LD, LC):
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).
☒N patunayan (ano ang Y☒N ?)

Talababa

baguhin
  1. ↑ 1.0 1.1 Merck Index, 11th Edition, 6002

Karagdagang Talababa

baguhin
  • 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.{{cite journal}}: CS1 maint: date auto-translated (link)

Mga kawing panlabas

baguhin
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