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10027-30-2

Copper phthalate is a chemical compound formed by the complexation of copper(II) ions with phthalate anions, known for its versatile applications in various industries.
Used in Wood Preservation Industry:
Copper phthalate is used as a wood preservative for its ability to protect against fungal decay and termites, particularly in marine and agricultural applications.
Used in Paint and Coating Industry:
Copper phthalate is used as a pigment in paints and coatings, enhancing their durability and performance.
Used in Organic Synthesis:
Copper phthalate is used as a catalyst in organic synthesis, facilitating various chemical reactions and improving the efficiency of the processes.
It is crucial to handle and dispose of copper phthalate with care due to its potential toxicity to aquatic organisms and possible health risks to humans if ingested or inhaled.

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  • 10027-30-2 Structure

  • Basic information

    1. Product Name: copper phthalate
    2. Synonyms: copper phthalate;Phthalic acid copper(II) salt;1,2-Benzenedicarboxylic acid, copper(2+) salt;Ai3-17215;Einecs 233-068-7
    3. CAS NO:10027-30-2
    4. Molecular Formula: 2C8H5O4*Cu
    5. Molecular Weight: 227.66096
    6. EINECS: 233-068-7
    7. Product Categories: N/A
    8. Mol File: 10027-30-2.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 378.3°Cat760mmHg
    3. Flash Point: 196.7°C
    4. Appearance: /
    5. Density: g/cm3
    6. Vapor Pressure: 2.14E-06mmHg at 25°C
    7. Refractive Index: N/A
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: copper phthalate(CAS DataBase Reference)
    11. NIST Chemistry Reference: copper phthalate(10027-30-2)
    12. EPA Substance Registry System: copper phthalate(10027-30-2)

  • 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: 10027-30-2(Hazardous Substances Data)

10027-30-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 10027-30-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,0,2 and 7 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 10027-30:
(7*1)+(6*0)+(5*0)+(4*2)+(3*7)+(2*3)+(1*0)=42
42 % 10 = 2
So 10027-30-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H6O4.Cu/c9-7(10)5-3-1-2-4-6(5)8(11)12;/h1-4H,(H,9,10)(H,11,12);/q;+2/p-2

10027-30-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name copper,phthalate

1.2 Other means of identification

Product number -
Other names copper(II) o-phthalate

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:10027-30-2 SDS

10027-30-2Relevant articles and documents

Relationship between the structures of Cu(II) complexes and their chemical transformations. XII. Are there only the split - off bonds activated during dehydration of copper carboxylates?

Langfelderova,Hodur

, p. 1009 - 1023 (2008/10/08)

The study of the thermal dehydration of the compounds CuX2nH2O, where X- were formate, salicylate or phtalate anions, was performed, including the observations of structural changes of compounds during their decomposition.

LIQUID-PHASE OXIDATION OF DIETHYL SULFIDE BY OXYGEN IN THE PRESENCE OF COPPER-CONTAINING CATALYSTS.

Barnakova,Mashkina,Kirik,Masagutov,Sharipov,Zagryatskaya,Suleimanova

, p. 712 - 715 (2008/10/08)

The activity of a copper-containing catalyst in the liquid-phase oxidation of diethyl sulfide by air was studied. It is established that in the formation of diethyl sulfoxide and diethylsulfone, high catalytic activity is possessed by copper(II) phenolates that contain electron donor substituents in the benzene ring.

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