Home Categories Organic Chemistry 2,3-Butanedione
A1219112

2,3-Butanedione , standardforGC,≥99.0%(GC) , 431-03-8

Synonym(s):
2,3-Butanedione, 2,3-Butadione, Dimethyldiketon, Dimethylglyoxal;Biacetyl;Diacetyl

CAS NO.:431-03-8

Empirical Formula: C4H6O2

Molecular Weight: 86.09

MDL number: MFCD00008756

EINECS: 207-069-8

Update time: 2022-07-08

PRODUCT Properties

Melting point: -4--2 °C
Boiling point: 88 °C(lit.)
Density  0.985 g/mL at 20 °C
vapor density  3 (vs air)
vapor pressure  52.2 mm Hg ( 20 °C)
FEMA  2370 | DIACETYL
refractive index  n20/D 1.394(lit.)
Flash point: 45 °F
storage temp.  Store at +2°C to +8°C.
solubility  200g/l
form  Liquid
color  Clear yellow
Odor at 1.00 % in propylene glycol. strong butter sweet creamy pungent caramel
Odor Type buttery
Odor Threshold 0.00005ppm
explosive limit 2.4-13.0%(V)
Water Solubility  200 g/L (20 ºC)
Merck  14,2966
JECFA Number 408
BRN  605398
Exposure limits ACGIH: TWA 0.01 ppm; STEL 0.02 ppm
NIOSH: TWA 5 ppb; STEL 25 ppb
Stability: Stable. Flammable. Incompatible with acids, strong bases, metals, reducing agents, oxidizing agents. Protect from moisture and water. Note low flashpoint.
InChIKey QSJXEFYPDANLFS-UHFFFAOYSA-N
LogP -1.340

Description and Uses

2,3-Butanedione, also known as Diacetyl, is a reactive diketone in artificial butter flavors. It is a water-soluble and volatile, alpha-diketone compound that has a buttery odor. Diacetyl occurs naturally in plants, fruits, coffee, honey, cocoa, and dairy products. It is a natural by-product of fermentation and is found in beer and wine. Diacetyl is also present in cigarette smoke.
Diacetyl can be synthesized by converting 2-butanone to an isonitroso compound and then hydrolyzing it with hydrochloric acid. Other methods for producing diacetyl include oxidation of 2-butanone over a copper catalyst at 300°C and dehydrogenation of 2,3-butanediol over a copper or silver catalyst. In addition, diacetyl can be synthesized through the acid catalyzed condensation of 1-hydroxyacetone and formaldehyde. Naturally occurring diacetyl is also available from starter distillate, a by-product of dairy product fermentation. Although diacetyl and starter distillates are liquids, they can be converted to a powdered form by encapsulating them within a solid material to prevent volatility. Diacetyl in powdered form is also found in flavorings that have been spray dried. The boiling point of diacetyl is 88°C with a calculated vapor pressure of 55 mmHg at 20°C.

2,3-Butanedione is a flavoring agent that is a clear yellow to yellowish green liquid with a strong pungent odor. It is chemically synthesized from methyl ethyl ketone. It is miscible in water, glycerin, alcohol, and ether, and in very dilute water solution it has a typical buttery odor and flavor. It is used as Carrier of aroma of butter, vinegar, coffee, and other foods. It is also used Inactivates aminopeptidase-N, precursor to α-diones, Cyclocondensation with amines has been used to form triazine and pteridine ring systems.

Safety

Symbol(GHS) 
GHS02,GHS05,GHS06,GHS08
Signal word  Danger
Hazard statements  H225-H302-H315-H317-H318-H331-H373
Precautionary statements  P210-P280-P301+P312-P304+P340+P311-P305+P351+P338-P314
Hazard Codes  F,Xn
Risk Statements  11-20/22-38-41-36/38-20/21/22-37/38
Safety Statements  9-16-26-37/39-36/37/39-39
RIDADR  UN 2346 3/PG 2
WGK Germany  2
RTECS  EK2625000
13
Autoignition Temperature 365 °C
TSCA  Yes
HazardClass  3
PackingGroup  II
HS Code  29141990
Toxicity LD50 orally in rats: 1580 mg/kg (Jenner)

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