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3-Butyn-2-one

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3-Butyn-2-one Basic information

Product Name:
3-Butyn-2-one
Synonyms:
  • Methyl ethynyl ketone
  • ETHYNYL METHYL KETONE
  • 1-BUTYN-3-ONE
  • 1-BUTYNE-3-ONE
  • 3-BUTYNE-2-ONE
  • 3-BUTYN-2-ONE
  • 3-Butyn-2-one 99%
  • 3-BUTYN-2-ONE, 98+%
CAS:
1423-60-5
MF:
C4H4O
MW:
68.07
EINECS:
215-834-2
Product Categories:
  • C3 to C6
  • Carbonyl Compounds
  • ketone
  • Acetylenes
  • Functionalized Acetylenes
  • Ketones
Mol File:
1423-60-5.mol
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3-Butyn-2-one Chemical Properties

Boiling point:
85 °C(lit.)
Density 
0.87 g/mL at 25 °C(lit.)
refractive index 
n20/D 1.406(lit.)
Flash point:
28 °F
storage temp. 
0-6°C
form 
Liquid
Specific Gravity
0.870
color 
Clear yellow to orange-brown
Water Solubility 
It is soluble in water.
BRN 
605353
CAS DataBase Reference
1423-60-5(CAS DataBase Reference)
NIST Chemistry Reference
3-Butyn-2-one(1423-60-5)
EPA Substance Registry System
3-Butyn-2-one (1423-60-5)
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Safety Information

Hazard Codes 
F,T+,T,Xi,E,Xn
Risk Statements 
28-36/37/38-11-15-10
Safety Statements 
45-36/37/39-28A-26-16-43-7/8-7/9-24/25
RIDADR 
UN 1992 3/PG 2
WGK Germany 
3
RTECS 
ES0875000
19
Hazard Note 
Highly Flammable/Highly Toxic
HazardClass 
3
PackingGroup 
II
HS Code 
29141900

MSDS

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3-Butyn-2-one Usage And Synthesis

Chemical Properties

clear yellow to orange-brown liquid

Chemical Properties

3-Butyn-2-one is a clear, colorless liquid that is chemically reactive. It has a boiling point of 85.0°C. The autoignition temperature for 3-butyn-2-one is 274°C. 3-Butyn-2-one has a penetrating odor and is a lacrimator. 3-Butyn-2-one has a penetrating odor and is a lacrimator.

Uses

3-Butyn-2-one was used in the synthesis of clerodane diterpenoid (+/-)-sacacarin. It was used as substrate in stereoselective, conjugate arylation mediated by gallium(III) chloride leading to (E)-α,β-unsaturated ketones.

Definition

ChEBI: Butyn-2-one is a methyl ketone and a terminal acetylenic compound. It is functionally related to a butan-2-one.

General Description

3-Butyn-2-one undergoes asymmetric double-Michael reaction with ortho-tosylamidophenyl malonate catalyzed by chiral aminophosphines to yield indolines. It undergoes double Michael reaction with nitrogen-containing tethered diacid to give pipecolic acid derivatives.

3-Butyn-2-one Preparation Products And Raw materials

Preparation Products

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