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2,3-Pentanedione

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2,3-Pentanedione Basic information

Product Name:
2,3-Pentanedione
Synonyms:
  • 2,3-Pentadione
  • 2,3-pentandione
  • 3-Pentanedione
  • Natural 2,3-Pentanedione
  • Acethylpropionyl
  • CH3C(O)C(O)C2H5
  • 2,3-PENTANEDITHIOL
  • 2 3-PENTANEDIONE 96+% FCC
CAS:
600-14-6
MF:
C5H8O2
MW:
100.12
EINECS:
209-984-8
Product Categories:
  • Pharmaceutical Raw Materials
  • ketone Flavor
  • Organics
Mol File:
600-14-6.mol
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2,3-Pentanedione Chemical Properties

Melting point:
-52 °C (lit.)
Boiling point:
110-112 °C (lit.)
Density 
0.957 g/mL at 25 °C (lit.)
vapor pressure 
28.5 hPa (20 °C)
FEMA 
2841 | 2,3-PENTANEDIONE
refractive index 
n20/D 1.404(lit.)
Flash point:
66 °F
storage temp. 
2-8°C
solubility 
60g/l
form 
Liquid
color 
very deep green-yellow
PH
4 (H2O)
Odor
at 1.00 % in dipropylene glycol. pungent sweet butter creamy caramel nutty cheese
Odor Type
buttery
explosive limit
1.8-10.9%(V)
Water Solubility 
60 g/L (15 ºC)
JECFA Number
410
BRN 
1699638
Exposure limits
NIOSH: TWA 9.3 ppb; STEL 31 ppb
Stability:
Stable. Highly flammable - store cool. Incompatible with strong oxidizing agents, reducing agents, strong bases.
InChIKey
TZMFJUDUGYTVRY-UHFFFAOYSA-N
LogP
-0.85
CAS DataBase Reference
600-14-6(CAS DataBase Reference)
NIST Chemistry Reference
2,3-Pentanedione(600-14-6)
EPA Substance Registry System
2,3-Pentanedione (600-14-6)
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Safety Information

Hazard Codes 
F,Xi
Risk Statements 
11-36/37/38
Safety Statements 
16-26-36-37/39
RIDADR 
UN 1224 3/PG 2
WGK Germany 
1
RTECS 
SA1850000
9-23
Autoignition Temperature
265 °C
TSCA 
Yes
HazardClass 
3
PackingGroup 
II
HS Code 
29141990
Hazardous Substances Data
600-14-6(Hazardous Substances Data)
Toxicity
LD50 orally in Rabbit: 3000 mg/kg LD50 dermal Rabbit > 2500 mg/kg

MSDS

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2,3-Pentanedione Usage And Synthesis

Chemical Properties

2,3-Pentanedione is a colourless or deep green-yellow colour liquid that has a somewhat sweet odor similar to quinone. This compound has a penetrating, buttery taste on dilution. It is used as flavoring agent or adjuvant.

Occurrence

2,3-Pentanedione occurs in butter, bread, milk, yogurt, chicken, meat, cocoa, coffee, potato chips, roasted almonds, pecans, beer, red and white wine, rum and whiskey. The organoleptic profile can be described as creamy, penetrating, cheesy, oily, sweet, buttery, almondlike, brown roasted, and somewhat caramellic, with a fruity nuance.

Uses

2,3-Pentanedione may be used as a reference standard in the determination of 2,3-pentanedione in beer samples using headspace-gas chromatographic technique (HS-GC).

Application

2,3-Pentanedione can be used as a reactant to synthesize:
Bisphenol derivatives by acid-catalyzed condensation reaction with phenols.
2-Ethyl-3-methyl-1H-indole by Pd-catalyzed reaction with aniline under reductive conditions.
2-Ethyl-3-methylquinoxaline by condensation reaction with o-phenylenediamine using citric acid as a catalyst.

Definition

ChEBI: 2,3-Pentanedione is an alpha-diketone that is pentane substituted at the 2- and 3-positions by oxo groups. It has a role as a flavouring agent. It is an alpha-diketone and a methyl ketone. It derives from a hydride of a pentane.

Preparation

By oxidation of methyl propyl ketone with excess NaNO2 and diluted HCl in the presence of hydroxylamine hydrochloride under a nitrogen blanket.

Aroma threshold values

Detection: 20 ppb. Aroma characteristics at 1.0%: buttery diacetyl-like, fermented dairy and creamy, popcorn buttery.

Taste threshold values

Taste characteristics at 1 to 5 ppm: sweet buttery, creamy, cheesy, slightly toasted dairy, with a rich baked goods nuance and a good mouthfeel.

General Description

2,3-Pentanedione (acetylpropionyl) is one of the aroma active compounds of cereal coffee brew.

Biochem/physiol Actions

Taste at 1-5.0 ppm

Safety Profile

Confirmed human carcinogen. Poison by intraperitoneal route. When heated to decomposition it emits acrid smoke and irritating fumes. See also NICKEL COMPOUNDS

2,3-Pentanedione Preparation Products And Raw materials

Raw materials

Preparation Products

2,3-PentanedioneSupplier

Henan Wei Yuan Biotechnology Co., Ltd. Gold
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