P1222

Potassium acetate

meets USP testing specifications

Manufacturer: Sigma Aldrich

CAS Number: 127-08-2

Select a Size

Pack Size SKU Availability Price
500 G P1222-500-G In Stock ₹ 18,683.95

P1222 - 500 G

₹ 18,683.95

In Stock

Quantity

1

Base Price: ₹ 18,683.95

GST (18%): ₹ 3,363.111

Total Price: ₹ 22,047.061

Agency

USP/NFmeets USP testing specifications

Quality Level

200

Assay

99.0-100.5%

form

crystalline

pH

7.0-9 (25 °C, 98.2 g/L)

solubility

H2O: soluble 98.2 g/L at 20 °C, colorless

density

1.57 g/cm3 at 25 °C (lit.)

application(s)

pharmaceutical (small molecule)

SMILES string

[K+].CC([O-])=O

InChI

1S/C2H4O2.K/c1-2(3)4;/h1H3,(H,3,4);/q;+1/p-1

Other Options

Image Product Name Manufacturer Price Range
50-180-5631
Sigma Aldrich Fine Chemicals Biosciences Potassium acetate United States Pharmacopeia (USP) Reference Standard | 127-08-2 | MFCD00012458 | 500MG
Sigma Aldrich Fine Chemicals Biosciences ₹ 39,408.94
NC2399776
eMolecules​ Potassium acetate | 127-08-2 | MFCD00012458 | 25g
eMolecules​ ₹ 2,591.61
50-180-5640
Sigma Aldrich Fine Chemicals Biosciences Potassium acetate 99.98% trace metals basis | 127-08-2 | MFCD00012458 | 25G
Sigma Aldrich Fine Chemicals Biosciences ₹ 25,469.50
NC2196648
eMolecules​ Potassium acetate | 127-08-2 | MFCD00012458 | 5kg
eMolecules​ ₹ 42,985.34
NC2303040
eMolecules​ POTASSIUMACETATE | 127-08-2 | MFCD00012458 | 500G
eMolecules​ --
50-492-859
Chem-Impex International, Inc. Potassium acetate | 127-08-2 | MFCD00012458 | 10KG
Chem-Impex International, Inc. ₹ 46,946.77
NC1604808
U.S. Pharmacopeia Potassium acetate, 127-08-2, MFCD00012458, 500 mg
U.S. Pharmacopeia ₹ 26,307.99
NC1600132
Chem-Impex International, Inc. Potassium acetate | 127-08-2 | MFCD00012458 | 250G
Chem-Impex International, Inc. ₹ 3,721.86
50-188-0136
Sigma Aldrich Fine Chemicals Biosciences Potassium acetate ReagentPlus(R), >=99.0% | 127-08-2 | MFCD00012458 | 500G
Sigma Aldrich Fine Chemicals Biosciences ₹ 7,101.48
50-188-0135
Sigma Aldrich Fine Chemicals Biosciences Potassium acetate ReagentPlus(R), >=99.0% | 127-08-2 | MFCD00012458 | 2.5KG
Sigma Aldrich Fine Chemicals Biosciences ₹ 20,019.33

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Description

  • Application: Study on the Freeze-Thaw Resistance of Concrete Pavements in Seasonally Frozen Regions.: This research examines the effectiveness of potassium acetate as a de-icing agent for concrete pavements, highlighting its role in improving the durability and longevity of infrastructure in cold climates. The study emphasizes the chemical′s ability to mitigate the adverse effects of freeze-thaw cycles on concrete (Zhao R et al., 2024).Optimization of Spore Production in Bacillus coagulans Using Response Surface Methodology Approach.: Highlighting the use of potassium acetate as a nutrient source in microbial cultures, this study details the optimization of growth conditions for Bacillus coagulans. The research provides insights into maximizing spore production for various biotechnological applications (Mirmajidi SH et al., 2024).Gene Expression of Ethanol and Acetate Metabolic Pathways in the Acinetobacter baumannii EmaSR Regulon.: Investigating the metabolic role of potassium acetate in bacterial physiology, this study examines how Acinetobacter baumannii utilizes this compound in its metabolic pathways. The research enhances understanding of bacterial adaptation and potential targets for antimicrobial strategies (Huang YW et al., 2024).Polyimide-Based Aqueous Potassium Energy Storage Systems Using Concentrated WiSE Electrolyte.: This article discusses the development of innovative energy storage systems using potassium acetate as a key component in electrolyte solutions. The study advances the field of energy storage technologies by demonstrating the electrolyte′s effectiveness in enhancing ionic conductivity and battery performance (Vardhini G et al., 2024).

SAFETY INFORMATION

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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H2O: soluble 98.2 g/L at 20 °C, colorless

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1S/C2H4O2.K/c1-2(3)4;/h1H3,(H,3,4);/q;+1/p-1

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CCCCCCCC\C=C/CCCCCCCC(=O)OCC(COP(O)(=O)OCCN)OC(=O)CCCCCCC\C=C/CCCCCCCC

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