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Sec-Butyl acetate

sec-Butyl acetate
Sec-butyl acetate
Ball-and-stick model of the sec-butyl acetate molecule
Names
Preferred IUPAC name
Butan-2-yl acetate
Other names
2-Butyl acetate
sec-Butyl acetate (no longer recommended)
sec-Butyl ester;
s-Butyl acetate;
sec-Butyl ester of acetic acid
1-Methylpropyl acetate
Identifiers
3D model (Jmol)
ChemSpider
ECHA InfoCard 100.003.001
PubChem CID
UNII
Properties
C6H12O2
Molar mass 116.16 g/mol
Appearance clear, liquid
Odor fruity
Density 0.87 g/cm3, liquid
Melting point −99 °C (−146 °F; 174 K)
Boiling point 112 °C (234 °F; 385 K)
0.80 g/100 mL
Vapor pressure 10 mmHg
Hazards
Main hazards Flammable
Safety data sheet External MSDS
Flash point 17 °C; 62 °F; 290 K
Explosive limits 1.7%-9.8%
US health exposure limits (NIOSH):
PEL (Permissible)
TWA 200 ppm (950 mg/m3)
REL (Recommended)
TWA 200 ppm (950 mg/m3)
IDLH (Immediate danger)
1700 ppm
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

sec-Butyl acetate, or s-butyl acetate, is a solvent commonly used as a solvent in lacquers and enamels, where it is used in the production of acyclic polymers, vinyl resins, and nitrocellulose. It is a clear flammable liquid with a sweet smell.

sec-Butyl acetate has three isomers that are also acetate esters: n-butyl acetate, isobutyl acetate, and tert-butyl acetate.

The first method of production of sec-butyl acetate was the esterification of sec-butanol and acetic anhydride It was experimentally determined and published in 1946 by Rolf Altschul.

The LD50 for rats is 13 g/kg. Exposure in humans to significant quantities of sec-butyl acetate can cause irritation to the eyes, mouth, throat, nose, and skin. Ingestion and inhalation of sec-butyl acetate can cause central nervous system depression producing symptoms of dizziness and disorientation.


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