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Key Documents

227129

Sigma-Aldrich

Cobalt(II) acetylacetonate

97%

Synonyme(s) :

2,4-Pentanedione cobalt(II) derivative, Bis(2,4-pentanedionato)cobalt, Co(acac)2, Cobaltous acetylacetonate

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About This Item

Formule linéaire :
Co(C5H7O2)2
Numéro CAS:
Poids moléculaire :
257.15
Numéro CE :
Numéro MDL:
Code UNSPSC :
12352103
ID de substance PubChem :
Nomenclature NACRES :
NA.23

Niveau de qualité

Pureté

97%

Forme

powder and chunks

Pertinence de la réaction

core: cobalt

Impuretés

≤3% water

Pf

165-170 °C (lit.)

Chaîne SMILES 

CC(=O)\C=C(\C)O[Co]O\C(C)=C/C(C)=O

InChI

1S/2C5H8O2.Co/c2*1-4(6)3-5(2)7;/h2*3,6H,1-2H3;/q;;+2/p-2/b2*4-3-;

Clé InChI

UTYYEGLZLFAFDI-FDGPNNRMSA-L

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Application


  • Cobalt (II)-Catalyzed Isocyanide Insertion Reaction with Amines: Details a synthetic method for forming ureas and azaheterocycles catalyzed by Cobalt(II) acetylacetonate, applicable in pharmaceutical synthesis (Zhu et al., 2014).

  • Cobalt‐Catalyzed C−H Functionalizations by Imidate Assistance: Describes a method using Cobalt(II) acetylacetonate for C-H functionalization, important for organic synthesis and material chemistry (Mei & Ackermann, 2016).

  • Cobalt (II) acetylacetonate covalently anchored onto magnetic mesoporous silica nanospheres: Focuses on its use as a catalyst for epoxidation of olefins, relevant for catalysis research (Li et al., 2015).

Cobalt(II) acetylacetonate can be used:
  • A precursor in the solvothermal synthesis of Co3O4 nanoparticles. These nanoparticles exhibit high electrochemical performance and are used as a potential supercapacitor material due to their excellent capacitance and cycling stability.
  • A precursor in the preparation of Co3O4 nanoparticles via hydrothermal method. The resulting Co3O4 nanoparticles exhibit a highly-uniform mesoporous structure and tunable sizes, making them promising for CO sensing applications.
  • A precursor for the growth of cobalt oxide thin films using Metal-Organic Chemical Vapor Deposition (MOCVD).

Mention d'avertissement

Danger

Classification des risques

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 1B Inhalation - Eye Dam. 1 - Repr. 1B - Resp. Sens. 1 - Skin Sens. 1

Code de la classe de stockage

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

dust mask type N95 (US), Eyeshields, Gloves


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Consulter la Bibliothèque de documents

Sujin Kim et al.
ChemSusChem, 10(17), 3473-3481 (2017-06-20)
Hybrid systems in which molecule-based active species are combined with nanoscale materials may offer valuable routes to enhance catalytic performances for electrocatalytic reactions. The development of rationally designed, cost-effective, efficient catalysts for the oxygen reduction reaction (ORR) is a crucial
Itziar Galarreta et al.
Nanomaterials (Basel, Switzerland), 8(2) (2018-01-26)
With the aim of studying the influence of synthesis parameters in structural and magnetic properties of cobalt-doped magnetite nanoparticles, Fe3-xCo
Hui Liu et al.
Scientific reports, 7(1), 11421-11421 (2017-09-14)
Alloying platinum (Pt) with suitable transition metals is effective way to enhance their catalytic performance for methanol oxidation reaction, and reduce their cost at mean time. Herein, we report our investigation on the synthesis of bimetallic platinum-cobalt (PtCo) alloy nanoparticles
Kinjal Gandha et al.
Nanotechnology, 26(7), 075601-075601 (2015-01-23)
Ferromagnetic FeCo nanocrystals with high coercivity have been synthesized using a reductive decomposition method. The sizes and shapes of the nanocrystals were found to be dependent on reaction parameters such as the surfactant ratio, the precursor concentration and the heating
Wei Chen et al.
ACS nano, 13(2), 1292-1308 (2019-01-12)
Noninvasive stimuli-responsive drug delivery using magnetic fields in conjunction with superparamagnetic nanoparticles offers the potential for the spatial and temporal control of drug release. When hyperthermia is not desired and control of the dosage is required, it is necessary to

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