Methoxypropane

Methoxypropane
Names
Preferred IUPAC name
1-Methoxypropane
Other names
Propane, 1-methoxy-
methyl propyl ether
Metopryl
Neothyl
propane, 1-methoxy
methyl n-propyl ether
Identifiers
CAS Number
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.008.327
EC Number
  • 209-158-7
PubChem CID
RTECS number
  • KO2280000
UNII
UN number 2612
InChI
  • InChI=1S/C4H10O/c1-3-4-5-2/h3-4H2,1-2H3 checkY
    Key: VNKYTQGIUYNRMY-UHFFFAOYSA-N checkY
  • InChI=1/C4H10O/c1-3-4-5-2/h3-4H2,1-2H3
SMILES
  • O(CCC)C
Properties
Chemical formula
 C4H10O
Molar mass 74.12
Density 0.7356 g/cm3
Boiling point 38.8 °C (101.8 °F; 311.9 K)
Solubility in water
 30.5 g/L
Refractive index (nD)
 1.35837 (14.3 °C)
Viscosity 0.3064 cP (0.3 °C)
Pharmacology
inhalation
Hazards
NFPA 704 (fire diamond)
NFPA 704 four-colored diamondHealth 0: Exposure under fire conditions would offer no hazard beyond that of ordinary combustible material. E.g. sodium chlorideFlammability 3: Liquids and solids that can be ignited under almost all ambient temperature conditions. Flash point between 23 and 38 °C (73 and 100 °F). E.g. gasolineInstability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazards (white): no code
0
3
0
Flash point < −20 °C (−4 °F; 253 K)
Explosive limits 1.9–11.8%
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

Methoxypropane, or methyl propyl ether, is an ether once used as a general anaesthetic.[1] It is a clear colorless flammable liquid with a boiling point of 38.8 °C.[2]

Marketed under the trade names Metopryl and Neothyl, methoxypropane was used as an alternative to diethyl ether because of its greater potency. Its use as an anaesthetic has since been supplanted by modern halogenated ethers which are much less flammable.

References

  1. ^ White, Mary Louise T.; Shane, Sylvan M.; Krantz, John C., Jr. "Anesthesia. XXI. Propyl methyl ether as an inhalation anesthetic in man", Anesthesiology, (1946), 7, 663-7.
  2. ^ Merck Index, 11th edition, 6031.


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