Sodium acetate
SIGALD/241245 - ACS reagent, ≥99.0%
Synonym: Acetic acid sodium salt
CAS Number: 127-09-3
Empirical Formula (Hill Notation): C2H3NaO2
Molecular Weight: 82.03
EC Number: 204-823-8
MDL Number: MFCD00012459
Linear Formula: CH3COONa
Product Type: Chemical
This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material.
This image depicts SKU: 241245-100G
This image depicts SKU: 241245-100G
This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material.
This image depicts SKU: 241245-500G
This image depicts SKU: 241245-500G
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This image depicts SKU: 241245-1KG
This image depicts SKU: 241245-1KG
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This image depicts SKU: 241245-5G
This image depicts SKU: 241245-5G
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This image depicts SKU: 241245-2.5KG
This image depicts SKU: 241245-2.5KG
| anion traces | chloride (Cl-): ≤0.002% |
| phosphate (PO43-): ≤0.001% | |
| sulfate (SO42-): ≤0.003% | |
| assay | ≥99.0% |
| autoignition temp. | 1112 °F |
| cation traces | Ca: ≤0.005% |
| Fe: ≤0.001% | |
| heavy metals: ≤0.001% (by ICP-OES) | |
| Mg: ≤0.002% | |
| form | solid |
| grade | ACS reagent |
| impurities | ≤0.01% insolubles |
| InChI | 1S/C2H4O2.Na/c1-2(3)4;/h1 |
| InChI key | VMHLLURERBWHNL-UHFFFAOYSA |
| loss | ≤1.0% loss on drying |
| mp | >300 °C (dec.) (lit.) |
| pH | 7.0-9.2 (25 °C, 5%) |
| pKa | 4.76 (acetic acid) |
| Quality Level | 200  |
| SMILES string | [Na+].CC([O-])=O |
| suitability | complies for IR spectroscopy |
| Application: | Sodium acetate can be used as a base to synthesize:• Oxazolones via Erlenmeyer Plochl condensation reaction of aromatic aldehydes and hippuric acid. • Cinnamic acids via Perkin reaction between aromatic aldehydes and acid anhydrides. A mixture of sodium acetate-acetic acid buffer can be employed in the polybromination of substituted imidazoles to synthesize polybrominated imidazoles. It can also be used as a catalyst in tandem Knoevenagel-Michael multicomponent reactions. |
| General description: | Sodium acetate is a hydrophilic organic compound that can be prepared by treating acetic acid with sodium carbonate or sodium hydroxide. It acts as neutralizing agent, catalyst, food additive, and buffer to maintain a specific pH. |
| Legal Information: | Redi-Dri is a trademark of Sigma-Aldrich Co. LLC |
| Other Notes: | Go to Redi-Dri™ Product Listing 791741 |
| Packaging: | 1 kg in poly bottle |
| Packaging: | 2.5 kg in poly drum |
| Packaging: | 5, 100, 500 g in poly bottle |
| RIDADR | NONH for all modes of transport |
| WGK Germany | WGK 1 |
| Purity | ≥99.0% |
| mp | >300 °C (dec.) (lit.) |
| UNSPSC | 12352300 |