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Cyclopentanone CAS:120-92-3

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CAS No.:

120-92-3

Grade:

Industrial Grade

Content:

99%

Port:

SHANGHIA

Brand:

Orient

Packaging:

25kg/bag,500kg/bag, customized

Price valid (until):

2025-12-26

Company Type:
Trader
Location:
China
Qualification:
Main Products:

pharmaceutical intermediates,peptides,electronic chemicals

  • Product Description

  • Seller Information

  • Inquiry History

  • Description
    Cyclopentanone Chemical Properties
    Melting point  -51 °C (lit.)
    Boiling point  130-131 °C (lit.)
    density  0.951 g/mL at 25 °C (lit.)
    vapor density  2.97 (vs air)
    vapor pressure  11.5 hPa (20 °C)
    FEMA  3910 | CYCLOPENTANONE
    refractive index  n20/D 1.437(lit.)
    Fp  87 °F
    storage temp.  Store below +30°C.
    solubility  9.18g/l slightly soluble
    form  Liquid
    color  Clear colorless to slightly yellow
    Odor Pleasant
    Odor Type minty
    biological source synthetic
    explosive limit 1.6-10.8%(V)
    Water Solubility  PRACTICALLY INSOLUBLE
    JECFA Number 1101
    Merck  14,2743
    BRN  605573
    Dielectric constant 16.0(-49℃)
    Stability: Stable. Incompatible with strong reducing agents, strong oxidizing agents, strong bases.
    LogP 0.7 at 25℃
    Surface tension 33.78mN/m at 298.15K
    CAS DataBase Reference 120-92-3(CAS DataBase Reference)
    NIST Chemistry Reference Cyclopentanone(120-92-3)
    EPA Substance Registry System Cyclopentanone (120-92-3)


    Cyclopentanone Usage And Synthesis
    Physical and Chemical Properties Cyclopentanone is also known Adipic Ketono. It is transparent colorless oily liquid. It has smell of special ether and also slightly mint-smell. It has a relative molecular mass being 84.12. It also has a relative density being 0.9487, melting point being-51.3 ℃, boiling point being 130.6 ℃, 23~24 ℃ (1.333 X 103Pa), the refractive index being 1.4366, and the flash point being 30 ℃. It is insoluble in water, soluble in alcohol, ether and acetone. It is narcotic at high concentrations. It can be obtained through oxidation of cyclopentanol. It can also be obtained through the heating of Adipic acid in the presence of Barium hydroxide. Cyclopentanone is also easily subject to polymerization especially in the presence of an acid. In the case of heating, it can participate in the following dehydration reactions, respectively producing 2-cyclopentylene cyclopentanone and 2'-cyclopentylene-2-cyclopentylene cyclopentanone:
    Shop Cyclopentanone CAS:120-92-3-Detailed Image 1
    Hydrogenation can produce double-cyclopentanol with further dehydration producing 2, 2-tetramethylene cyclopentanone.
    Shop Cyclopentanone CAS:120-92-3-Detailed Image 2
    Cyclopentanone is mainly used for the manufacturing of drugs, biological agents, pesticides and rubber additives.
    Aldehydes, ketones can react with diazoalkane and have the nitrogen atoms lost, generating two carbonyl compounds and epoxy compounds. When the aldehydes, ketones molecules contain electron-withdrawing groups, the reactivity is increased will boost the generation of the epoxy compound. The ketone molecule, with the increase of the hydrocarbon group, also mainly generates epoxy compound. Cyclic ketones, instead, will have ring expansion reactions. The bigger the hydrocarbyl group of the diazoalkane is, the more carbonyl compounds can be obtained.
    The order of the ketone reactivity is consistent with its nucleophilic substitution order:
    Cl3CCOCH3> ClCH2COCH3> CH3COCH3> CH3COC6H5> cyclohexanone> cyclopentanone> cycloheptanone> cyclooctanone.
    The main purpose 1, Take the n-valeraldehyde and cyclopentanone as raw material, and first go through aldol condensation reaction and further dehydration reaction to obtain pentylene cyclopentanone, then followed by selective catalytic hydrogenation to obtain pentyl cyclopentanone. Pentyl cyclopentanone has strong floral and fruity aroma as well as nuances of jasmine. It can be used in the formulation of daily chemical flavor with the usage amount being less than 20%. IFRA has no restrictions.
    2, Take n-hexanal and cyclopentanone as the raw material, first have condensation, and then perform selective hydrogenation reaction to obtain hexyl cyclopentanone. Hexyl cyclopentanone has strong jasmine smell accompanied by fruit nuances and can be used in perfume fragrance as well as the formulation of other kinds of fragrance with the usage amount being less than 5%. IFRA has no restrictions.
    3, Take the 1-pentene or 1-heptene obtained by the cracking of paraffin or dehydration of the corresponding alcohol as the raw material, in the presence of t-butyl peroxide as the initiator, have addition reaction of the free radical group with cyclopentanone, generating 2-pentyl cyclopentanone (or 2-heptyl-cyclopentanone) with oxidation and ring expansion reaction to become δ-lactone (or δ-Dodecalactone).
    4 Synthesis route with cyclopentanone being the starting material is of the greatest industrial production value. Cyclopentanone is first had aldol condensation reaction with n-valeraldehyde with the dehydration products further undergoing condensation and the selective hydrogenation to generate 2-pentyl cyclopentanone. It finally undergoes oxidation and ring expansion to become δ-decalactone.
    5, δ-decalactone is mainly used in the formulation of edible food flavor. It is considered with the characteristic flavor of the natural cream. Before its emergence, perfumers had long been limited to application of monomer spices such as butanedione and vanillin monomers to be as the major raw material for the deployment of butter flavor. But it is generally recognized that the formulated butter flavor is worse than natural products in the respects of both taste or flavor respects. Only after the use of δ-decalactone can it have realistic cream flavor, especially in the case of using δ-Dodecalactone and δ-decalactone in combination for being as the main flavor raw material which can further improve the flavor and effect of the formulated cream spice.
    6, Take cyclopentanone and pentanal as raw materials, have condensation to produce 2-(1-hydroxy) pentyl cyclopentanone which is then reacted with dimethyl malonate and hydrolyzed at 160~180 ℃, go through decarboxylation, esterification to obtain methyl dihydrojasmonate. Methyl dihydrojasmonate is the edible flavor provided by the GB2760-1996 of China for temporary application. Its aroma is better than the natural methyl jasmonate. Its property is also relatively stable.



    Shop Cyclopentanone CAS:120-92-3-Detailed Image 3

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    ——  Q&A  ——

    Q1:Do you provide sample?

    A: Yes, we can provide free sample, you only need pay the shipping cost.

    Q2: What is the lead time?

    A: For stock goods, it usually take about 5-7 days by air, 15-30 days by sea,For customized products, the delivery time needs to be confirmed based on the actual situation.

    Q3: How can I buy? What is the payment method?

    A: You can contract us through Email or you can browse our website:orientchem.cc, we have bank transfer,

    A:We attach great importance to after-sales service of our products. If there are any quality issues, please contact us within 30 days of receiving the goods and we will handle returns and exchanges for you.



    Certificates

    Basic Info
    Product Name:

    Cyclopentanone

    Other Name:

    Cyclopentanone;Adipic ketone;Dumasin;Ketocyclopentane;Ketopentamethylene;Adipin keton;NSC 4122;6: PN: WO2007101224 PAGE: 36 claimed sequence;1800084-96-1

    CAS No.:

    120-92-3

    Molecular Formula:

    C5H8O

    InChIKeys:

    InChIKey=BGTOWKSIORTVQH-UHFFFAOYSA-N

    Molecular Weight:

    84.118

    Exact Mass:

    84.12

    EC Number:

    204-435-9

    UNII:

    220W81TN3S

    ICSC Number:

    0427

    NSC Number:

    4122

    UN Number:

    2245

    DSSTox ID:

    DTXSID3029154

    Color/Form:

    WATER-WHITE, MOBILE LIQUID

    HScode:

    2914 29 00

    Characteristics
    PSA:

    17.1

    XLogP3:

    0.38

    Appearance:

    Cyclopentanone appears as a clear colorless liquid with a petroleum-like odor. Flash point 87°F. Less dense than water and insoluble in water. Vapors heavier than air.

    Density:

    0.94869 g/cm3 @ Temp: 20 °C

    Melting Point:

    -51.3 °C

    Boiling Point:

    130.6 °C @ Press: 760 Torr

    Flash Point:

    26°C

    Refractive Index:

    n 20/D 1.437(lit.)

    Water Solubility:

    H2O: 9.18g/l slightly soluble

    Storage Conditions:

    Flammables area

    Vapor Pressure:

    11.5 hPa (20 °C)

    Vapor Density:

    Relative vapour density (air = 1): 2.3

    Toxicity:

    Intraperitoneal-mouse LD50: 1950 mg/kg; subcutaneous-Mouse LD50: 2600 mg/kg.

    Flammability characteristics:

    It is flammable in case of fire, high temperature and with burning producing irritated smoke.

    Explosive limit:

    1.6-10.8%(V)

    Odor:

    DISTINCTIVE ETHEREAL ODOR, SOMEWHAT LIKE PEPPERMINT

    OH:

    2.94e-12 cm3/molecule*sec

    Henrys Law Constant:

    1.00e-05 atm-m3/mole

    Experimental Properties:

    POLYMERIZES EASILY, ESP IN PRESENCE OF ACIDS

    Air and Water Reactions:

    Highly flammable. Insoluble in water.

    Reactive Group:

    Ketones

    Reactivity Alerts:

    Highly Flammable

    Reactivity Profile:

    CYCLOPENTANONE polymerizes easily, especially in the presence of acids. Can react with oxidizing materials, i.e. hydrogen peroxide. (NTP, 1992)

    Peroxide Forming Chemical:

    Cyclopentanone|D*: Other compounds that may form peroxides|4 samples had 1-4 ppm peroxide; age >1 yrs|Management of time-sensitive chemicals (JCHAS)

    Physical Dangers:

    The vapour is heavier than air.

    Hazard Identification

    Classification of the substance or mixture

    Flammable liquids, Category 3

    Skin irritation, Category 2

    Eye irritation, Category 2

    GHS label elements, including precautionary statements

    Pictogram(s)
    Signal word

    Warning

    Hazard statement(s)

    H226 Flammable liquid and vapour

    H315 Causes skin irritation

    H319 Causes serious eye irritation

    Precautionary statement(s)
    Prevention

    P210 Keep away from heat, hot surfaces, sparks, open flames and other ignition sources. No smoking.

    P233 Keep container tightly closed.

    P240 Ground and bond container and receiving equipment.

    P241 Use explosion-proof [electrical/ventilating/lighting/...] equipment.

    P242 Use non-sparking tools.

    P243 Take action to prevent static discharges.

    P280 Wear protective gloves/protective clothing/eye protection/face protection/hearing protection/...

    P264 Wash ... thoroughly after handling.

    Response

    P303+P361+P353 IF ON SKIN (or hair): Take off immediately all contaminated clothing. Rinse affected areas with water [or shower].

    P370+P378 In case of fire: Use ... to extinguish.

    P302+P352 IF ON SKIN: Wash with plenty of water/...

    P321 Specific treatment (see ... on this label).

    P332+P317 If skin irritation occurs: Get medical help.

    P362+P364 Take off contaminated clothing and wash it before reuse.

    P305+P351+P338 IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing.

    Storage

    P403+P235 Store in a well-ventilated place. Keep cool.

    Disposal

    P501 Dispose of contents/container to an appropriate treatment and disposal facility in accordance with applicable laws and regulations, and product characteristics at time of disposal.

    Other hazards which do not result in classification

    no data available

    Handling and Storage

    Precautions for safe handling

    NO open flames, NO sparks and NO smoking. Handling in a well ventilated place. Wear suitable protective clothing. Avoid contact with skin and eyes. Avoid formation of dust and aerosols. Use non-sparking tools. Prevent fire caused by electrostatic discharge steam.

    Conditions for safe storage, including any incompatibilities

    Fireproof. Separated from acids. Cool. Keep in the dark. Keep in a well-ventilated room. Store only if stabilized.

  • Seller Information
    Business Type:

    Trader

    Main Products:

    pharmaceutical intermediates,peptides,electronic chemicals

    Location:

    Room 102, 1st Floor, East Office Building, No. 45 Pengwan Road, Qianwan Bonded Port Area, Qingdao Zone, China (Shandong) Pilot Free Trade Zone

    Payment Terms:

    100% TT in advance

    Average lead Time:

    10

    Total Annual Revenue:

    $10 million-$25 million

    Total Employees:

    51-100

    Year of Establishment:

    2024

    A reliable supplier is like insurance.

    We are mainly specilized in supply of pharmaceutical intermediates, electronic chemicals,food additives, and other fine chemical products.
    Integrity is the foundation, quality is life. We would like to work together with you to build a greener and brighter future.

    Website: orientchem.cc
    Email: scarlett@orientchem.cc
    WhatsApp: +86 17753254221

  • Inquiry History
    5 Inquiries
    Country Product Purchase Quantity Date Posted
    India

    Cyclopentanone

    1000 KG Aug 27, 2024
    United States

    Cyclopentanone

    10 MT Aug 1, 2023
    United States

    Cyclopentanone

    1 MT Oct 7, 2024
    United Kingdom

    cyclopentanone

    1000 MT Jun 11, 2024
    United Kingdom

    cyclopentanone

    50 KG Jun 9, 2026
    Post an enquiry for this product
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