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Glacial Acetic Acid (99% min) - Taiwan
- Origin
- : Taiwan
- CAS Number
- : 64-19-7
- HS Code
- : 29152100
Basic Info
- IUPAC Name
- : acetic acid
- Molecular Formula
- : C2H4O2
- Molecular Weight (g/mol)
- : 60.0500
- Synonyms & Trade Names
- : Glacial acetic acid; Ethanoic acid; Methanecarboxylic acid
- Purity / Assay (%)
- : 99.5% min
- Grade / Quality Level
- : Industrial Grade
- Physical Form
- : Liquid
- Concentration
- : Pure substance
- Appearance / Color
- : Clear to slightly colored liquid
- Odor
- : Vinegar-like sharp
- Melting Point (°C)
- : 17.0000
- Boiling Point (°C)
- : 118
- Density (g/cm³)
- : 1.0490
- Solubility in Water
- : Miscible
- Signal Word
- : Danger
- UN Number
- : 2789
- GHS Hazard Class
- : Flammable; Skin corrosive; Eye corrosive
- H-Statements
- : H226|H290|H314
- P-Statements
- : P210|P234|P260|P264|P271|P273|P280|P301+P330+P331
- REACH Status
- : Registered
- Drug Precursor Status
- : Non-precursor
- Storage Class (GHS)
- : 8
- Storage Conditions
- : Cool, dry; away from oxidizers and bases
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Brief Overview
Glacial Acetic acid is the concentrated variant of acetic acid, also known as ethanoic acid, with the molecular formula CH3COOH. It acts as a weak monoprotic acid, readily releasing a proton from its acid functional group (-COOH) to form the acetate anion, a conjugate base. Functioning as a polar protic solvent, it easily dissolves and mixes with other polar solvents like water. However, its polar nature makes it insoluble and unable to mix with non-polar solvents such as octane.
When used as a primary reagent, acetic acid readily creates various organic reagents like acetyl chloride and ethanol through substitution and reduction reactions, respectively. Moreover, it can corrode metals like iron, magnesium, and zinc, producing hydrogen gas and metal acetates. Notably, aluminum develops a protective layer of aluminum oxide, granting it acid resistance and making aluminum tanks a suitable choice for transporting acetic acid. Alternatively, high-density polyethylene (HDPE) drums are also effective transport vessels due to their resistance against the effects of acetic acid.
Manufacturing Process
Method 1: Methanol Carbonylation
The synthesis of acetic acid involves methanol carbonylation, where the introduction of metal carbonyl into methanol occurs through either the rhodium-catalyzed Monsanto process or the iridium-catalyzed Cativa process. However, the advancement of the iridium-catalyzed Cativa process rendered the Monsanto process obsolete. The Cativa process, known for its economic and environmentally sustainable nature, swiftly became the primary method for producing acetic acid.
Method 2: Acetaldehyde Oxidation
Another approach to acetic acid production entails oxidizing acetaldehyde, obtained from the oxidation of butane and hydration of ethylene through the Wacker process. The resulting crude acetaldehyde undergoes purification via extractive distillation followed by fractional distillation. This refined acetaldehyde then undergoes further oxidation to yield acetic acid.
Method 3: Fermentation Techniques
Acetic acid synthesis also involves oxidative fermentation utilizing acetic acid bacteria Acetobacter in alcoholic content or anaerobic fermentation employing anaerobic bacteria Acetobacterium. The Acetobacter method proves more cost-effective for acetic acid production compared to other fermentation methods.
