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  • Cyclopentanone, C5H8O, CAS No. C120-92-3
  • Cyclopentanone, C5H8O, CAS No. C120-92-3
  • Cyclopentanone, C5H8O, CAS No. C120-92-3
Cyclopentanone, C5H8O, CAS No. C120-92-3

Cyclopentanone, C5H8O, CAS No. C120-92-3

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Chemical NameCyclopentanone
CAS Number120-92-3
Molecular FormulaC5H8O
Purity>99%, 99%, and 98%
Packaging Details25 litres Drum
SynonymsKetocyclopentane, Adipic ketone
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Specifications of Cyclopentanone, C5H8O, CAS No. C120-92-3

Chemical Identifiers

Chemical Name Cyclopentanone
CAS Number 120-92-3
Molecular Formula C5H8O
Synonyms Ketocyclopentane, Adipic ketone
EC Number 204-435-9
IUPAC Name Cyclopentanone

General Details

Purity >99%, 99%, and 98%
Packaging Details 25 litres Drum

Chemical Properties

Molecular Weight (g/mol) 84.12 g/mol
Density 0.95 g/cm³
Melting Point -58.2°C
Boiling Point 130.6°C
Solubility in water 9.175 g/L
Vapor pressure, kPa 1.51
Refractive index 1.4366
Flash Point 26°C
Auto Ignition Temperature 445°C
Surface tension 34 mN/m
Vapor density (air=1) 2.3
Critical Temperature 241°C
Critical Pressure 4.6 MPa
Dipole Moment 3.28 D
Heat of Fusion -236.5 kJ/mol
Heat of Vaporization 42.6 kJ/mol
Heat of Combustion -2870 kJ/mol

Physical Properties

Physical Form Liquid
Color Clear Colourless
Odor Pepermint like
Shelf Life 4-5 Years
Features
  • Colourless liquid with low toxicity
  • It has similar properties to gasoline and ethanol
  • It has a role as a Maillard reaction product
  • Insoluble in water, soluble in alcohol & acetone
Applications
  • Application include pharmaceuticals,perfumes,etc
  • Used as flavouring agents
  • Used as a solvent in Paints removers
  • Raw material for cosmetic industry
Product Description
    Packaging Details Price
    25 kg Drum Rs 8,750
    50 kg Drum Rs 17,500
    180 kg Drum Rs 64,800

     

     

    Production of Cyclopentanone
    Cyclopentanone is the product of furfural rearrangement in an aqueous system. Since the aldol-condensation reaction is conducted in an aqueous solution all these biomass-derived reactants can be applied as water solutions formed in the processes of their preparation. The aldol condensation of furfural with cyclopentanone is at low concentration of base and molar ratio of reactants 2:1 highly selective and after 40–80 min of reaction at a temperature of 40–100 °C more than 95 mol% yield of 2,5-bis (2-furylmethylidene) cyclopentan-1-one was obtained. When instead of furfural as a reactant HMF was used higher than 98 mol% yield of 2,5-bis (5-hydroxymethyl-2-furylmethylidene) cyclopentan-1-one was achieved.

    ASTM Testing Standard
    • D1089 Method of Test for Carbonyl Content of Butadiene
    • D1193 Specification for Reagent Water
    • D1612 Test Method for Acetone in Methanol
    • D2119 Test Method for Aldehydes in Styrene Monomer
    • D2191 Test Method for Acetaldehyde Content of Vinyl Acetate
    • E60 Practice for Analysis of Metals, Ores, and Related Materials by Spectrophotometry
    • E180 Practice for Determining the Precision of ASTM Methods for Analysis and Testing of Industrial and Specialty Chemicals
    • E300 Practice for Sampling Industrial Chemicals

    Storage and Handling
    • Precautions for safe handling
    Avoid contact with skin and eyes.
    Avoid inhalation of vapour or mist.
    Keep away from sources of ignition - No smoking.
    Take measures to prevent the build up of electrostatic charge.
    • Conditions for safe storage
    Store in cool place.
    Keep container tightly closed in a dry and well-ventilated place.
    Containers which are opened must be carefully resealed and kept upright to prevent leakage

    Incompatible Materials
    Strong oxidizing agents, Strong bases, Strong reducing agents

    Fire fighting
    • Suitable extinguishing media Use water spray, alcohol-resistant foam, dry chemical or carbon dioxide
    • Advice for firefighters Wear self-contained breathing apparatus for firefighting if necessary
    • Use water spray to cool unopened containers

    First Aid
    • If inhaled - If breathed in, move person into fresh air. If not breathing, give artificial respiration. Consult a physician.
    • In case of skin contact - Wash off with soap and plenty of water. Consult a physician.
    • In case of eye contact - Rinse thoroughly with plenty of water for at least 15 minutes and consult a physician.
    • If swallowed - Do NOT induce vomiting. Never give anything by mouth to an unconscious person. Rinse mouth with water. Consult a physician.

    Hazard Statement
    • Flammable liquid and vapour.
    • Causes skin irritation.
    • Causes serious eye irritation

    Precaution
    • Wash face, hands and any exposed skin thoroughly after handling
    • Wear protective gloves/protective clothing/eye protection/face protection
    • Keep away from heat/sparks/open flames/hot surfaces. - No smoking
    • Keep container tightly closed
    • Ground/bond container and receiving equipment
    • Use explosion-proof electrical/ventilating/lighting/equipment
    • Use only non-sparking tools
    • Take precautionary measures against static discharge

    Uses
    Cyclopentanone is common precursor to fragrances, especially those related to jasmine and jasmone. Examples include 2-pentyl- and 2-heptylcyclopentanone.It is a versatile synthetic intermediate, being a precursor to cyclopentobarbital. Cyclopentanone is also used to make cyclopentamine, the pesticide pencycuron, and pentethylcyclanone.

Product Photos
  • Cyclopentanone, C5H8O, CAS No. C120-92-3
  • Cyclopentanone, C5H8O, CAS No. C120-92-3
  • Cyclopentanone, C5H8O, CAS No. C120-92-3
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