Movatterモバイル変換


[0]ホーム

URL:


Jump to content
WikipediaThe Free Encyclopedia
Search

Ethyl formate

From Wikipedia, the free encyclopedia
Ethyl formate
Ethyl formate
Ethyl formate
Names
Preferred IUPAC name
Ethyl formate
Systematic IUPAC name
Ethyl methanoate
Identifiers
3D model (JSmol)
906769
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard100.003.384Edit this at Wikidata
EC Number
  • 203-721-0
RTECS number
  • LQ8400000
UNII
UN number1190
  • InChI=1S/C3H6O2/c1-2-5-3-4/h3H,2H2,1H3 checkY
    Key: WBJINCZRORDGAQ-UHFFFAOYSA-N checkY
  • InChI=1/C3H6O2/c1-2-5-3-4/h3H,2H2,1H3
    Key: WBJINCZRORDGAQ-UHFFFAOYAO
  • O=COCC
Properties
HCOOCH2CH3
Molar mass74.079 g·mol−1
AppearanceColorless liquid[1]
Odorfruity[1]
Density0.917 g/cm3
Melting point−80 °C; −112 °F; 193 K
Boiling point54.0 °C (129.2 °F; 327.1 K)
9% (17.78 °C)[1]
Vapor pressure200 mmHg (20°C)[1]
−43.00·10−6 cm3/mol
Hazards
Flash point−20 °C; −4 °F; 253 K[1]
Explosive limits2.8% - 16.0%[1]
Lethal dose or concentration (LD, LC):
1850 mg/kg (rat, oral)
1110 mg/kg (guinea pig, oral)
2075 mg/kg (rabbit, oral)[2]
10,000 ppm (cat, 1.5 hr)
8000 ppm (rat, 4 hr)[2]
NIOSH (US health exposure limits):
PEL (Permissible)
TWA 100 ppm (300 mg/m3)[1]
REL (Recommended)
TWA 100 ppm (300 mg/m3)[1]
IDLH (Immediate danger)
1500 ppm[1]
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
checkY verify (what is checkY☒N ?)
Chemical compound

Ethyl formate is anester formed whenethanol (analcohol) reacts withformic acid (acarboxylic acid). Ethyl formate has the characteristic smell ofrum and is partially responsible for the flavor ofraspberries,[3] occurring naturally in some plant oils, fruits, and juices.

Exposure

[edit]

Ethyl formate isgenerally recognized as safe by theU.S. Food and Drug Administration.[4]

According to theU.S Occupational Safety and Health Administration (OSHA), ethyl formate can irritate eyes, skin,mucous membranes, and therespiratory system of humans and other animals; it is also acentral nervous systemdepressant.[5] In industry, it is used as a solvent forcellulose nitrate,cellulose acetate, oils, and greases. It can be used as a substitute foracetone; workers may also be exposed to it under the following circumstances:[5]

OSHA considers a time-weighted average of 100parts per million (300 milligrams per cubic meter) over an eight-hour period as thepermissible exposure limit. TheU.S. National Institute for Occupational Safety and Health (NIOSH) also considers a time-weighted average of 100 ppm over an eight-hour period as therecommended exposure limit.[6]

In space

[edit]

Ethyl formate has been identified in dust clouds in an area of the Milky Way galaxy calledSagittarius B2. It is among 50 molecular species identified using the30 metreIRAM radiotelescope.[3]

References

[edit]
  1. ^abcdefghiNIOSH Pocket Guide to Chemical Hazards."#0278".National Institute for Occupational Safety and Health (NIOSH).
  2. ^ab"Ethyl formate".Immediately Dangerous to Life or Health Concentrations.National Institute for Occupational Safety and Health.
  3. ^abSample, Ian (21 April 2009)."Galaxy's centre tastes of raspberries and smells of rum, say astronomers".The Guardian.Archived from the original on 6 July 2017. Retrieved2009-04-21.
  4. ^ab"Alternative fumigants: Ethyl Formate".University of California. Archived fromthe original on 2009-05-30. Retrieved2009-04-25.
  5. ^ab"Occupational Safety and Health Guideline for Ethyl Formate".OSHA. Archived fromthe original on 2009-04-14. Retrieved2009-04-25.
  6. ^CDC - NIOSH Pocket Guide to Chemical HazardsArchived 2017-12-19 at theWayback Machine.
Methyl esters
Ethyl esters
Propyl esters
Butyl esters
Amyl esters
Hexyl esters
Phenyl esters
Heptyl esters
Benzyl esters
Molecules
Diatomic








Triatomic
Four
atoms
Five
atoms
Six
atoms
Seven
atoms
Eight
atoms
Nine
atoms
Ten
atoms
or more
Deuterated
molecules
Unconfirmed
Related
Retrieved from "https://en.wikipedia.org/w/index.php?title=Ethyl_formate&oldid=1315061085"
Categories:
Hidden categories:

[8]ページ先頭

©2009-2025 Movatter.jp