Product Overview

Acetic Acid Glacial ACS Grade is a high-purity organic acid with critical importance in advanced chemical research and industrial processing. As a pure, concentrated form of acetic acid, this reagent represents a fundamental organic compound characterized by its remarkable versatility and chemical reactivity. The glacial designation indicates its extremely pure state, with minimal water content, enabling precise analytical and synthetic applications across multiple scientific disciplines.

Chemically, this compound represents a critical carboxylic acid with significant potential for complex organic transformations. Its molecular structure features a characteristic carboxyl group, which provides exceptional reactivity and enables numerous sophisticated chemical reactions essential in advanced research and industrial synthesis processes. The ACS Grade certification ensures the highest standard of chemical purity, making it an indispensable tool for rigorous scientific investigation and technical applications.

Key Properties

• Chemical Formula: CH3COOH
• Molecular Weight: 60.05 g/mol
• Boiling Point: 118°C
• Melting Point: 16°C
• Specific Gravity: 1.049
• Flash Point: 39°C
• Appearance: Colorless, clear liquid
• Solubility: Miscible with water, alcohol, ether
• Chemical Stability: High stability under standard conditions

Common Applications

• Chemical Synthesis: Utilized as a critical intermediate in complex organic reaction pathways, enabling sophisticated molecular transformations through its reactive carboxyl group and exceptional chemical versatility.
• Laboratory Analysis: Serves as a precise titration standard and analytical reagent for quantitative chemical measurements, providing exceptional accuracy in research and quality control processes.
• Industrial Cleaning: Employed as a powerful descaling and decontamination agent in industrial equipment, effectively removing mineral deposits and organic residues from complex mechanical systems.
• Solvent Extraction: Functions as an advanced extraction solvent in research environments, facilitating separation and purification of organic compounds through selective dissolution mechanisms.
• Organic Reaction Catalyst: Acts as a crucial catalyst in numerous organic chemistry transformations, enabling stereospecific molecular rearrangements and complex synthetic strategies.

Safety Precautions

Acetic Acid Glacial requires specialized handling protocols due to its corrosive nature and potential chemical reactivity. Always utilize dedicated chemical fume hoods with appropriate ventilation when manipulating this reagent, ensuring minimal exposure to vapors and potential splashing.

Storage demands strict environmental control, necessitating sealed glass or specialized chemical-resistant containers positioned in cool, dry locations away from direct sunlight and potential ignition sources. Maintain consistent temperatures between 15-25°C to preserve chemical integrity and minimize potential decomposition.

Personal protective equipment is mandatory, including chemical-resistant nitrile gloves, full-face splash protection, and laboratory coat. In case of accidental exposure, immediately flush affected areas with copious amounts of water and seek medical consultation. Keep appropriate neutralizing agents such as sodium bicarbonate solution readily accessible in laboratory environments.

Benefits

ACS Grade certification guarantees exceptional purity levels, providing researchers and industrial chemists with a consistently reliable chemical reagent suitable for the most demanding analytical and synthetic applications. The rigorous quality control ensures minimal impurity interference and maximum reproducibility in complex chemical processes.

The exceptional chemical versatility of this glacial acetic acid enables sophisticated molecular transformations across diverse scientific domains. Its precise formulation and consistent performance make it an invaluable tool for advanced research, offering unparalleled reliability in critical chemical investigations and industrial synthesis strategies.