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37110-24-0

DIMEDONE DIOXIME is a chemical compound that belongs to the class of oximes, which are organic compounds containing the functional group C=N-OH. It is derived from the compound dimedone, a cyclic ketone, with the addition of two oxime groups resulting in its formation. This chemical is recognized for its chelating properties, particularly its ability to complex with metal ions, especially transition metals such as copper.

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  • (NE)-N-[(5E)-5-hydroxyimino-3,3-dimethyl-cyclohexylidene]hydroxylamine

    Cas No: 37110-24-0

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  • 37110-24-0 Structure

  • Basic information

    1. Product Name: DIMEDONE DIOXIME
    2. Synonyms: METHONE DIOXIME;DIMETHYLDIHYDRORESORCINOL DIOXIME;DIMEDONE DIOXIME;5,5-DIMETHYL-1,3-CYCLOHEXANEDIONE DIOXIME;(NE)-N-[(5E)-5-HYDROXYIMINO-3,3-DIMETHYL-CYCLOHEXYLIDENE]HYDROXYLAMINE;Dimedone Dioxime [for Determination of Co];5,5-Dimethyl-1,3-cyclohexanedione Dioxime Dimethyldihydroresorcinol Dioxime Methone Dioxime;[for DeterMination of Co]
    3. CAS NO:37110-24-0
    4. Molecular Formula: C8H14N2O2
    5. Molecular Weight: 170.21
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 37110-24-0.mol

  • Chemical Properties

    1. Melting Point: 173 °C
    2. Boiling Point: 329.2°Cat760mmHg
    3. Flash Point: 202.5°C
    4. Appearance: /
    5. Density: 1.21g/cm3
    6. Vapor Pressure: 3.55E-05mmHg at 25°C
    7. Refractive Index: 1.551
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: DIMEDONE DIOXIME(CAS DataBase Reference)
    11. NIST Chemistry Reference: DIMEDONE DIOXIME(37110-24-0)
    12. EPA Substance Registry System: DIMEDONE DIOXIME(37110-24-0)

  • 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: 37110-24-0(Hazardous Substances Data)

37110-24-0 Usage

Uses

Used in Analytical Chemistry:
DIMEDONE DIOXIME is used as a reagent for the determination and extraction of metal ions in solution. Its chelating nature allows for effective binding and separation of metal ions, which is crucial in various analytical processes.
Used in the Development of Novel Materials:
DIMEDONE DIOXIME is studied for its potential use in the development of new materials. Its ability to form complexes with metal ions can contribute to the creation of materials with unique properties and applications.
Used as a Catalyst in Organic Synthesis:
DIMEDONE DIOXIME is also utilized as a catalyst in organic synthesis. Its interaction with metal ions can facilitate and enhance the rate of chemical reactions, making it a valuable component in the synthesis of various organic compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 37110-24-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,1,1 and 0 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 37110-24:
(7*3)+(6*7)+(5*1)+(4*1)+(3*0)+(2*2)+(1*4)=80
80 % 10 = 0
So 37110-24-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H14N2O2/c1-8(2)4-6(9-11)3-7(5-8)10-12/h11-12H,3-5H2,1-2H3/b9-6-,10-7+

37110-24-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name Dimedone Dioxime [for Determination of Co]

1.2 Other means of identification

Product number -
Other names DIMETHYLDIHYDRORESORCINOL DIOXIME

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:37110-24-0 SDS

37110-24-0Upstream product

37110-24-0Relevant articles and documents

Green and highly selective protocol for the synthesis of oximes

Ghosh, Pranab,Subba, Raju

, p. 529 - 532 (2013/11/06)

A green and efficient protocol has been developed for the synthesis of either exclusively a monoxime or exclusively a dioxime from a host of 1,2-dicarbonyl compounds on silica.

Catalytic effect of wet molecular sieve 3A in dry media on syntheses of oximes and 1,3-dioximes

Bigdeli, Mohammadali,Rahmati, Abbas

, p. 605 - 607 (2007/10/03)

A simple, efficient and eco-friendly method has been developed for the condensation of hydroxylamine hydrochloride with aldehydes, ketones and 1,3-diketones in the presence of powdered molecular sieves (3A) as catalyst. Aldoximes, ketoximes and 1,3-dioximes were obtained in excellent yields.

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