282774

Rhodium(III) acetylacetonate

97%

Manufacturer: Sigma Aldrich

CAS Number: 14284-92-5

Synonym(S): 2,4-Pentanedione rhodium(III) derivative, Rh(acac)3

Select a Size

Pack Size SKU Availability Price
250 MG 282774-250-MG In Stock ₹ 14,674.20
1 G 282774-1-G In Stock ₹ 40,281.90
5 G 282774-5-G In Stock ₹ 2,27,849.70

282774 - 250 MG

₹ 14,674.20

In Stock

Quantity

1

Base Price: ₹ 14,674.20

GST (18%): ₹ 2,641.356

Total Price: ₹ 17,315.556

Quality Level

100

Assay

97%

form

solid

reaction suitability

reagent type: catalyst

mp

263-264 °C (lit.)

SMILES string

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

InChI

1S/3C5H8O2.Rh/c3*1-4(6)3-5(2)7;/h3*3,6H,1-2H3;/q;;;+3/p-3/b3*4-3+;

InChI key

DGOINFUDFBWCMX-MUCWUPSWSA-K

Other Options

Image Product Name Manufacturer Price Range
50-901-12213
Strem, An Ascensus Company CAS# 14284-92-5. 250mg. Rhodium(III) acetylacetonate, 97+% (99.9%-Rh). MFCD00083144
Strem, An Ascensus Company ₹ 29,158.85
282774
Rhodium(III) acetylacetonate
Sigma Aldrich ₹ 14,674.20 - ₹ 2,27,849.70
AI67562
14284-92-5 | Rhodium(III) acetylacetonate
A2B Chem ₹ 2,139.00 - ₹ 14,545.20

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Description

  • General description: Rhodium(III) acetylacetonate is a yellowcrystalline compound composed of rhodium atoms coordinated with three acetylacetonate ligands. It iswidely used in the field of catalysis, organic electronics and to prepare Rhcomplexes. It is soluble inorganic solvents.[1]
  • Application: Rhodium(III) acetylacetonate can be used:As a precursor to synthesize Rh nanocrystals with catalytic activities.As an efficient catalyst for the α-alkylation of ketones, β-alkylation of secondary alcohols, and the alkylation of amines with primary alcohols.To prepare highly phosphorescent complexes for organic light-emitting devices.To synthesize the Rh2P NCs supported on carbon (Rh2P/C) by a one-step solvothermal method via a direct reaction between Rh(acac)3 and tri-n-octylphosphine (TOP). The resultant electrocatalyst exhibited remarkable performance for both the hydrogen evolution reaction and the oxygen evolution reaction, surpassing the capabilities of Rh/C and Pt/C catalysts for water splitting .To prepare Single-atom Rh/N-doped carbon electrocatalyst for the oxidation of formic acid.To synthesize Pt–Rh NWs as highly efficient electrocatalysts toward ethanol oxidation reaction (EOR) for Direct ethanol fuel cells. The electrocatalyst demonstrated improved catalytic activities, primarily attributed to the presence of Rh, which enhances its ability to resist poisoning.

SAFETY INFORMATION

Pictograms

GHS08,GHS07

Signal Word

Warning

Hazard Statements

H302 + H312 + H332,H315,H319,H335,H361

Precautionary Statements

P280 - P301 + P312 - P302 + P352 + P312 - P304 + P340 + P312 - P305 + P351 + P338 - P308 + P313

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Repr. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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100

Assay:
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form:
solid

reaction suitability:
reagent type: catalyst

mp:
263-264 °C (lit.)

SMILES string:
CC(=O)\C=C(/C)O[Rh](O\C(C)=C\C(C)=O)O\C(C)=C\C(C)=O

InChI:
1S/3C5H8O2.Rh/c3*1-4(6)3-5(2)7;/h3*3,6H,1-2H3;/q;;;+3/p-3/b3*4-3+;

InChI key:
DGOINFUDFBWCMX-MUCWUPSWSA-K

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

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

InChI key:
KLFRPGNCEJNEKU-FDGPNNRMSA-L

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InChI:
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KLFRPGNCEJNEKU-FDGPNNRMSA-L

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__

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__

mp:
__

SMILES string:
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InChI:
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InChI key:
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