Pharmaceutical Grade Glacial Acetic Acid Medical Grade Glacial Acetic Acid Complies with Pharmacopoeia Standards Disinfectant and Preservative Active Pharmaceutical Ingredient 500ml per Bottle

Shaanxi Active Pharmaceutical Ingredient Glacial Acetic Acid | Glacial Acetic Acid API | Pharmaceutical Grade Glacial Acetic Acid | Pharmaceutical Raw Material Glacial Acetic Acid

Medicinal Glacial Acetic Acid Medicinal Acetic Acid Medical Glacial Acetic Acid National Medicine Approval Number Glacial Acetic Acid/Acetic Acid

02.26.002 Glacial Acetic Acid (Acetic Acid) 500g Bottle Pharmaceutical Grade

02.28.001 Propylene Glycol 500ml Bottle Pharmaceutical Grade

02.28.003 Propylene Glycol 25kg Pharmaceutical Grade

Xi'an Pharmaceutical Grade Glacial Acetic Acid (Acetic Acid) Pharmaceutical Raw Material

Chinese Name Glacial Acetic Acid

English Name Acetic acid

Chinese Aliases Acetic acid; Glacial acetic acid; Acid (food grade); Glacial acetic acid; Glacial acetic acid (food grade); Acetic acid, anhydrous; Acetic acid (food grade)

Glacial Acetic Acid CAS: 64-19-7

EINECS Number 200-580-7

Glacial Acetic Acid Molecular Formula C2H4O2

Glacial Acetic Acid Molecular Weight 60.05

Physicochemical Properties Appearance Colorless transparent liquid with a pungent odor.

Glacial Acetic Acid Melting Point 16.635°C

Glacial Acetic Acid Boiling Point 117.9°C

Relative Density 1.0492

Refractive Index 1.3716

Flash Point 57°C

[Indications] This product in different concentrations is used to treat various superficial fungal skin infections, irrigate wounds, and treat corns and warts. Glacial acetic acid can be used as a caustic agent.

[Drug Classification] Disinfectant and Preservative - Glacial Acetic Acid

Glacial Acetic Acid Uses: Mainly used in the preparation of acetic anhydride, vinyl acetate, acetate esters, metal acetates, cellulose acetate, etc. Used in the production of ethyl acetate, food flavorings, wine flavorings, etc. Used as an analytical reagent, solvent, and soaking agent.

Pharmaceutical Grade Glacial Acetic Acid Medical Grade Glacial Acetic Acid Complies with Pharmacopoeia Standards Disinfectant and Preservative Active Pharmaceutical Ingredient 500ml per Bottle

Glacial acetic acid, scientifically known as acetic acid (Acetic acid), is a common organic acid widely used in the chemical industry, food processing, and pharmaceutical industry. In pharmaceutical preparations, glacial acetic acid, as an acidic solution, is often used to adjust the pH of drug formulations, clean equipment, and serve as a solvent or buffer for some drugs. Pharmaceutical grade glacial acetic acid must meet strict quality standards to ensure its safety and efficacy in drug production.

According to the provisions of the Chinese Pharmacopoeia (CP edition), pharmaceutical grade glacial acetic acid must meet the following quality standards:

1. Appearance:

Pharmaceutical grade glacial acetic acid should be a colorless or slightly yellow liquid with a strong sour taste and the characteristic pungent odor of acetic acid. Its appearance should be clear and transparent, free of any visible impurities.

2. Identification:

Identification tests are usually conducted using infrared spectroscopy (IR) or other chemical methods. Pharmaceutical grade glacial acetic acid must be proven to be acetic acid (Acetic acid) and not other impurities. The identification method requires acetic acid to have specific spectral characteristics within ultraviolet, infrared, and other wavelength ranges.

3. Purity and Content Determination:

The purity of pharmaceutical grade glacial acetic acid should be no less than 99.5%. Conventional purity tests are performed using titration methods, particularly by titrating with a standard sodium hydroxide (NaOH) solution to determine the acetic acid content. The pharmacopoeia specifies its acidity standard, with acidity calculated as a percentage of milligrams of acetic acid.

4. Moisture Content:

Due to the hygroscopic nature of acetic acid, the moisture content of pharmaceutical grade glacial acetic acid must be strictly controlled, generally not exceeding 1%, to ensure its stability and purity in formulations.

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