ChemicalBook > CAS DataBase List > 3-Pentanone

3-Pentanone

Product Name
3-Pentanone
CAS No.
96-22-0
Chemical Name
3-Pentanone
Synonyms
PENTAN-3-ONE;DIETHYL KETONE;DEK;ETHYL KETONE;3-Pentanon;PROPIONE;Ethyl propionyl;ZED2EK;(C2H5)2CO;Metacetone
CBNumber
CB5270897
Molecular Formula
C5H10O
Formula Weight
86.13
MOL File
96-22-0.mol
More
Less

3-Pentanone Property

Melting point:
-42 °C (lit.)
Boiling point:
101.5 °C (lit.)
Density 
0.813 g/mL at 25 °C (lit.)
vapor density 
3 (vs air)
vapor pressure 
20 mm Hg ( 28 °C)
refractive index 
n20/D 1.392(lit.)
Flash point:
55 °F
storage temp. 
Store below +30°C.
solubility 
water: slightly soluble
form 
Liquid
color 
Clear colorless
Odor
at 0.10 % in propylene glycol. ethereal acetone
Relative polarity
0.265
PH
6.2 (50g/l, H2O, 20℃)
explosive limit
1.6-7.7%(V)
Odor Type
ethereal
Water Solubility 
50 g/L (20 ºC)
Merck 
14,3121
BRN 
635749
Exposure limits
TLV-TWA 705 mg/m3 (200 ppm) (ACGIH).
Dielectric constant
17.3(14℃)
Stability:
Stable. Highly flammable. Readily forms explosive mixtures with air. Incompatible with strong bases, reducing agents, strong oxidizing agents.
InChIKey
FDPIMTJIUBPUKL-UHFFFAOYSA-N
LogP
0.85 at 25℃
CAS DataBase Reference
96-22-0(CAS DataBase Reference)
NIST Chemistry Reference
3-Pentanone(96-22-0)
EPA Substance Registry System
3-Pentanone (96-22-0)
More
Less

Safety

Hazard Codes 
F,Xi
Risk Statements 
11-37-66-67
Safety Statements 
9-16-25-33
RIDADR 
UN 1156 3/PG 2
OEB
A
OEL
TWA: 200 ppm (705 mg/m3)
WGK Germany 
1
RTECS 
SA8050000
Autoignition Temperature
845 °F
TSCA 
Yes
HS Code 
2914 19 90
HazardClass 
3
PackingGroup 
II
Hazardous Substances Data
96-22-0(Hazardous Substances Data)
Toxicity
LD50 orally in rats: 2.1 g/kg, Smyth et al., Arch. Ind. Hyg. Occup. Med. 10, 61 (1954)
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Hazard statements

H225Highly Flammable liquid and vapour

H319Causes serious eye irritation

H335May cause respiratory irritation

H336May cause drowsiness or dizziness

Precautionary statements

P210Keep away from heat/sparks/open flames/hot surfaces. — No smoking.

P233Keep container tightly closed.

P240Ground/bond container and receiving equipment.

P241Use explosion-proof electrical/ventilating/lighting/…/equipment.

P242Use only non-sparking tools.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

More
Less

N-Bromosuccinimide Price

Sigma-Aldrich
Product number
8.03605
Product name
Diethyl ketone
Purity
for synthesis
Packaging
1L
Price
$60.9
Updated
2024/03/01
Sigma-Aldrich
Product number
8.03605
Product name
Diethyl ketone
Purity
for synthesis
Packaging
100ML
Price
$62.6
Updated
2024/03/01
Sigma-Aldrich
Product number
127604
Product name
3-Pentanone
Purity
ReagentPlus , ≥99.0% (GC)
Packaging
4l
Price
$263
Updated
2024/03/01
Sigma-Aldrich
Product number
127604
Product name
3-Pentanone
Purity
ReagentPlus?, ≥99.0% (GC)
Packaging
18L
Price
$692
Updated
2024/03/01
TCI Chemical
Product number
P0061
Product name
3-Pentanone
Purity
>98.0%(GC)
Packaging
25mL
Price
$22
Updated
2024/03/01
More
Less

3-Pentanone Chemical Properties,Usage,Production

Description

Diethyl ketone is a colorless liquid with anacetone-like odor (smells like nail-polish remover). Odorthreshold 2.8 ppm. Molecular weight=86.15; Specificgravity (H2O:1)=0,81 at 25℃; Boiling point=101.6℃;Freezing/Melting point=242℃; Vapor pressure 535 mmHg at 25℃; Flash point=12.8℃ (oc); Autoignitiontemperature=452℃. Explosive limits: LEL=1.6%;UEL=6.4%. Hazard Identification (based on NFPA-704 MRating System): Health 1, Flammability 3, Reactivity 0.Moderately soluble in water.

Chemical Properties

3-Pentanone (also known as diethyl ketone) is a member of the class of compounds known as ketones. It is a colorless liquid ketone with an odor like that of acetone. It is soluble in about 25 parts water, but miscible with organic solvents.3-pentanone is an acetone and ethereal tasting compound and can be found in a number of food items such as strawberry guava, ceylon cinnamon, beech nut, and pak choy, which makes 3-pentanone a potential biomarker for the consumption of these food products.

Uses

Diethyl ketone is used as a solvent, inmedicine, and in organic synthesis.

Uses

3-Pentanone is mainly used as a solvent in paint and a precursor to vitamin E. It is used as a reagent to synthesize ethyl 2-cyano-3,3-diethylacrylate by Knoevenagel condensation. It also shows anticonvulsant effect in several types of mouse seizure models. It serves as an intermediate in the manufacture of pharmaceuticals.

Definition

ChEBI: Pentan-3-one is a pentanone that is pentane carrying an oxo group at position 3. It has been isolated from Triatoma brasiliensis and Triatoma infestans. It has a role as an animal metabolite.

General Description

3-Pentanone is a clear colorless liquid with an acetone-like odor. Flash point 55°F. Less dense than water. Vapors heavier than air.

Air & Water Reactions

Highly flammable. Slightly soluble in water

Reactivity Profile

3-Pentanone is incompatible with the following: Strong oxidizers, alkalis, mineral acids, (hydrogen peroxide + nitric acid) .

Health Hazard

Liquid causes eye burn. Vapor irritates eyes, nose and throat; can cause headache, dizziness, nausea, weakness, and loss of consciousness.

Toxicology

Diethyl ketone is a mild narcotic compoundas well as an irritant. Its acute toxicity is lessthan that of methyl propyl ketone. Exposureto 80,000 ppm for 4 hours was fatal to rats.
LD50 value, oral (rats): 2140 mg/kg.

Fire Hazard

HIGHLY FLAMMABLE: Will be easily ignited by heat, sparks or flames. Vapors may form explosive mixtures with air. Vapors may travel to source of ignition and flash back. Most vapors are heavier than air. They will spread along ground and collect in low or confined areas (sewers, basements, tanks). Vapor explosion hazard indoors, outdoors or in sewers. Runoff to sewer may create fire or explosion hazard. Containers may explode when heated. Many liquids are lighter than water.

Flammability and Explosibility

Highly flammable

Safety Profile

Moderately toxic by routes. A skin and eye irritant. Mutation data reported. Dangerous fre hazard when exposed to heat or flame; can react vigorously with oxidzing materials. To fight fire, use alcohol foam, foam, CO2, dry chemical. Reacts with hydrogen peroxide + nitric acid to form a shockand heat sensitive explosive peroxide. When heated to decomposition it emits acrid smoke and irritating fumes. See also KETONES.

Synthesis

Ketonic decarboxylation route
3-Pentanone is produced by ketonic decarboxylation of propanoic acid using metal oxide catalysts:
2 CH3CH2CO2H → (CH3CH2)2CO + CO2 + H2O
in the laboratory, the reaction can be conducted in a tube furnace.
Other way to make 3-pentanone: Acetone + very strong base and then + methylating agent -> butanone. Butanone + very strong base, then + methylating agent -> mixture of 3-methylbutanone and 3-pentanone.
Synthesis of 3-pentanone from 1-propanol over CeO2–Fe2O3 catalysts
Vogel's Textbook of Practical Organic Chemistry

Synthesis

3-Pentanone's two synthesis methods : 1) from Propyl alcohol. 2) from Propionic acid.

Potential Exposure

Drug,Mutagen, Primary Irritant. This compound is used as a solvent; in organic synthesis and making medicines.

First aid

If this chemical gets into the eyes, remove anycontact lenses at once and irrigate immediately for at least15 min, occasionally lifting upper and lower lids. Seek medical attention immediately. If this chemical contacts theskin, remove contaminated clothing and wash immediatelywith soap and water. Seek medical attention immediately. Ifthis chemical has been inhaled, remove from exposure,begin rescue breathing (using universal precautions, including resuscitation mask) if breathing has stopped and CPR ifheart action has stopped. Transfer promptly to a medicalfacility. When this chemical has been swallowed, get medical attention. Give large quantities of water and inducevomiting. Do not make an unconscious person vomit.

Shipping

3-Pentanone requires a shipping label of“FLAMMABLE LIQUID.” It falls in Hazard Class 3 andPacking Group II.

Purification Methods

Dry it with anhydrous CaSO4 or CuSO4, and distil from P2O5 under N2 or under reduced pressure. Further purification is by conversion to the semicarbazone (recrystallise to constant m 139o, from EtOH) which, after drying in vacuo over CaCl2 and paraffin wax, is refluxed for 30minutes with excess oxalic acid, then steam distilled and salted out with K2CO3. Dry with Na2SO4 and distil [Cowan et al. J Chem Soc 171 1940]. [Beilstein 1 IV 3279.]

Incompatibilities

Violent reaction with oxidizers, causingfire and explosion hazard. Forms explosive mixture withair. Incompatible with strong acids, aliphatic amines.Attacks many plastics, rubber, and coatings. May accumulate static electrical charges, and may cause ignition of itsvapors.

Waste Disposal

Incineration; molten salt treatment.

More
Less

3-Pentanone Suppliers

Beckmann-Kenko GmbH
Tel
+49 4241 9308 88
Fax
+49 4241 9308 89
Email
info@beckmann-kenko.com
Country
Germany
ProdList
478
Advantage
62
Dr. Ehrenstorfer GmbH
Tel
--
Fax
--
Email
info@analytical-standards.com
Country
Germany
ProdList
5545
Advantage
66
MERCK KGAA
Tel
--
Fax
--
Email
service@merckgroup.com
Country
Germany
ProdList
43
Advantage
58
Merck Millipore
Tel
--
Fax
--
Email
ccc@merckgroup.com
Country
Germany
ProdList
2008
Advantage
58
Stockmeier Chemie Gmbh & Co. KG.
Tel
--
Fax
--
Email
info@stockmeier.de
Country
Germany
ProdList
35
Advantage
58
CHEMOS GmbH & Co. KG
Tel
--
Fax
--
Email
chemos@chemos.de
Country
Germany
ProdList
6727
Advantage
58
Alfa Aesar, Thermo Fisher Scientific
Tel
--
Fax
--
Email
es@alfa.com
Country
Germany
ProdList
5123
Advantage
58
HPC Standards GmbH
Tel
--
Fax
--
Email
chulze@hpc-standards.com
Country
Germany
ProdList
2139
Advantage
58
ABCR GmbH & CO. KG
Tel
--
Fax
--
Email
info@abcr.de
Country
Germany
ProdList
6831
Advantage
75
BASF Group
Tel
--
Fax
--
Email
info@basf-vc.de
Country
Germany
ProdList
357
Advantage
30
Service Chemical Inc.
Tel
--
Fax
--
Email
sales@chemos-group.com
Country
Germany
ProdList
6350
Advantage
71
BASF Aktiengesellschaft
Tel
--
Fax
--
Country
Germany
ProdList
520
Advantage
81
Merck Schuchardt OHG
Tel
--
Fax
--
Email
schuchardt-vertrieb@merck.de
Country
Germany
ProdList
5827
Advantage
74
More
Less

View Lastest Price from 3-Pentanone manufacturers

Hebei Weibang Biotechnology Co., Ltd
Product
3-Pentanone 96-22-0
Price
US $10.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
100 mt
Release date
2024-11-13
Hebei Mojin Biotechnology Co., Ltd
Product
3-Pentanone 96-22-0
Price
US $0.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
50000KG/month
Release date
2023-08-24
Career Henan Chemical Co
Product
3-Pentanone 96-22-0
Price
US $1.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
10000KGS
Release date
2019-12-31

96-22-0, 3-PentanoneRelated Search:


  • 3-Pentanon
  • DEK
  • Diathylketon
  • Diethylcetone
  • diethylcetone(french)
  • Diethylketon
  • Ethyl propionyl
  • Diethyl Ketone Propione
  • DIETHYL KETONE FOR SYNTHESIS
  • 3-Pentanone, standard for GC,>99.5%(GC)
  • Protein DEK
  • ketone,3-Pentanone
  • 3-Pentanone for HPLC, 96%
  • 3-Pentanone ReagentPlus(R), >=99.0% (GC)
  • 3-Oxopentane
  • ZED2EK
  • (C2H5)2CO
  • 1,3-Dimethylacetone
  • 3-Pentanone (DEK)
  • ethylpropionyl
  • Metacetone
  • Methacetone
  • Pentan-3-on
  • Pentanon-3
  • Pentanone-3
  • 3-PENTANONE, 96%, HPLC GRADE
  • 3-PENTANONE, REAGENTPLUS, >=99%
  • 3-PENTANONE 99+%
  • 3-PENTANON OEKANAL
  • 3-PENTANONE, STANDARD FOR GC
  • DiethylKetone,Certified
  • 3-Pentanone,98%
  • DIETHYL KETONE ( 3-PENTANONE )
  • pentanone,3-pentanone
  • pentan-3-one diethyl ketone
  • 3-Pentanone, 98%, pure
  • 3-Pentanone, 98% 500ML
  • 3-Pentanone, pure, 98%
  • ETHYL KETONE
  • DIMETHYLACETONE
  • DIETHYL KETONE
  • PROPIONE
  • PENTAN-3-ONE
  • 3-PENTANONE
  • 3-Pentanone, 99.5%
  • 3-Pentanone&gt
  • DIETHYL KETONE FOR SYNTHESIS 1 L
  • DIETHYL KETONE FOR SYNTHESIS 100 ML
  • Diethylketone, puriss, 99%
  • Pentan-3-One, Technical, Fisher Chemical
  • Diethyl Ketone (3-Pentanone) extrapure, 99%
  • ANTI-DEK(C-TERMINAL) antibody produced in rabbit
  • Oseltamivir Impurity 70 (3-Pentanone)
  • Diethyl Ketone 99% For Synthesis
  • 3-Pentanone in Carbon disulfide
  • 96-22-0
  • 96220
  • C2H5COC2H5