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CAS

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3304-24-3

Cyclohexanone, 2-(1-hydroxy-1-methylethyl)-5-methyl-, also known as 5-methyl-2-(1-hydroxy-1-methylethyl)-cyclohexanone or 5-methyl-2-isopropylidene-cyclohexanone, is an organic compound with the molecular formula C10H18O. It is a colorless to pale yellow liquid with a density of 0.92 g/cm3 and a boiling point of 228-230°C. Cyclohexanone, 2-(1-hydroxy-1-methylethyl)-5-methyl- is a derivative of cyclohexanone, featuring a methyl group at the 5-position and an isopropylidene group at the 2-position. It is used as a synthetic intermediate in the production of various chemicals, pharmaceuticals, and fragrances. Due to its reactivity, it is important to handle Cyclohexanone, 2-(1-hydroxy-1-methylethyl)-5-methyl- with care, following proper safety guidelines.

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  • 3304-24-3 Structure

  • Basic information

    1. Product Name: Cyclohexanone, 2-(1-hydroxy-1-methylethyl)-5-methyl-
    2. Synonyms: Cyclohexanone, 2-(1-hydroxy-1-methylethyl)-5-methyl-
    3. CAS NO:3304-24-3
    4. Molecular Formula: C10H18O2
    5. Molecular Weight: 0
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 3304-24-3.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 263.6°Cat760mmHg
    3. Flash Point: 109.5°C
    4. Appearance: /
    5. Density: 1g/cm3
    6. Vapor Pressure: 0.00143mmHg at 25°C
    7. Refractive Index: 1.471
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: Cyclohexanone, 2-(1-hydroxy-1-methylethyl)-5-methyl-(CAS DataBase Reference)
    11. NIST Chemistry Reference: Cyclohexanone, 2-(1-hydroxy-1-methylethyl)-5-methyl-(3304-24-3)
    12. EPA Substance Registry System: Cyclohexanone, 2-(1-hydroxy-1-methylethyl)-5-methyl-(3304-24-3)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 3304-24-3(Hazardous Substances Data)

3304-24-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3304-24-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,0 and 4 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3304-24:
(6*3)+(5*3)+(4*0)+(3*4)+(2*2)+(1*4)=53
53 % 10 = 3
So 3304-24-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H18O2/c1-7-4-5-8(9(11)6-7)10(2,3)12/h7-8,12H,4-6H2,1-3H3

3304-24-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-hydroxypropan-2-yl)-5-methylcyclohexan-1-one

1.2 Other means of identification

Product number -
Other names 8-hydroxy-p-menthan-3-one

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:3304-24-3 SDS

3304-24-3Downstream Products

3304-24-3Relevant articles and documents

Essential oil composition and allelopathic effect of the Brazilian lamiaceae Hesperozygis ringens (Benth.) epling and Hesperozygis rhododon epling

Von Poser, Gilsane L.,Menut, Chantal,Toffoli, Maria E.,Verin, Pierre,Sobral, Marcos,Bessiere, Jean-Marie,Lamaty, Gerard,Henriques, Amelia T.

, p. 1829 - 1832 (2007/10/03)

Samples of Hesperozygis ringens (Benth.) Epling and Hesperozygis rhododon Epling essential oils were analyzed by a combination of analytical techniques: capillary gas chromatography, liquid/ solid chromatography, GC/MS coupling, and NMR spectroscopy. Twenty-four components have been identified representing altogether more than 95% of the oil content. The oil of H. ringens is constituted mainly by pulegone (79.2%) accompanied by several oxygenated derivatives (pulegone oxides, 1.2%; 8-hydroxy-p-menth-3-one, 1.3%; and 8-hydroxy-p-menth-4-en-3-one, 3.7%); that of H. rhododon contains menthone and pulegone as main compounds in almost comparable amounts (43.4% and 29.6%, respectively). Tests carried out on lettuce seeds using alcoholic extracts of the two species showed significant antigerminating properties mainly for H. ringens. The same activity was observed with its essential oil.

Biotransformation of terpenic compounds by fungi. I. Metabolism of R-(+)-pulegone

Ismaili-Alaoui,Benjilali,Buisson,Azerad

, p. 2349 - 2352 (2007/10/02)

R-(+)-Pulegone 1 is converted by several fungal strains to new regioselectively hydroxylated compounds. Epoxidation of the double bond does not seem to be responsible for the main observed hydroxylation pattern.

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