Dextrose Anhydrous Pharma IP

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MOQ : 1000 Kilograms

Dextrose Anhydrous Pharma IP Specification

Type
Pharmaceutical Grade

Form
Powder

Processing
Refined

Purity(%)
99.5%

Weight
25 kg

Color
White

Shelf Life
36 Months

Packaging
Bag

Pack Size
25 kg

Pack Type
HDPE Bag

Physical State
Solid

Flavor
Sweet

Dextrose Anhydrous Pharma IP Trade Information

Minimum Order Quantity
1000 Kilograms

Supply Ability
500 Kilograms Per Day

Delivery Time
1-2 Days

About Dextrose Anhydrous Pharma IP

Introduction :

Dextrose Anhydrous is produced by re-dissolving Dextrose Monohydrate, refining, evaporation and re-crystallization by seed crystals at elevated temperature.

It is separated by centrifugation, washing and drying. M/S.UNIVERSAL STARCH CHEM ALLIED LTD., manufactures Dextrose Anhydrous-IP.

Application :

Pharmaceutical : Dextrose Anhydrous is formulated with vitamins and Minerals and sold in packets or containers or used during convalescent periods of physical stress by patients, athletes and students. In medical formulations Dextrose is used in tableting (salt tablets) and as a raw material in the fermentation industry for bio-chemical synthesis of antibiotics (penicillin, streptomycin etc.) and vitamin C. via Sorbitol.

Fermentation industry : Dextrose serves as a raw material in the manufacture of citric acid, amino acids, enzymes, lactic acid and ethanol.

Chemical processes : Sorbitol and mannitol methyglucoside, gluconic acid, gluconates also are produced from various chemical reactions with Dextrose Monohydrate.

Dextrose Intravenous Injections:

Dextrose Injection is a sterile solution of Dextrose in water for Injection.
Thus Dextrose is a widely used product and its uses have increased over 100 fold. Best quality of Dextrose is produced by improved process equipments, refining techniques at rigid control of processing conditions at the most modern plant at Dondaicha, Dist Dhulia (M.S.).

Specification :

Determination	I.P. LIMITS	Results
Description	A white crystalline powder.	Complies
Identification	When heated it melts, swells up & burns & an odor of burnt sugar is perceptible. Dissolve 0.1 g in 10 ml of water, add 3 ml potassium cupri-tartrate solution; The solution is blue and clear. Heat to boiling; a copious red precipitate is formed,	Complies
Appearance and odour of Solution	Dissolve 10.0g in 15 ml of water. The solution is clear. not more intensely coloured than reference solution BYS7,and is odourless.	Complies
Acidity or alkalinity	NMT 0.15 ml of 0.1 M NaOH per 6 gm of the substance.	0.095
Specific Optical Rotation (10% W/V solution)	52.50 / -53.30	+52.89
Arsenic	NMT 1 ppm	Complies
Heavy metals	NMT 5 ppm	Complies
Chloride	NMT 125 ppm.	Complies
Sulphate	NMT 200 ppm .	Complies
Sulphite	Conforms	Complies
Barium	Conforms	Complies
Foreign sugars, soluble starch and dextrins	Conforms	Complies
Sulphated ash	NMT 0.10	0.038
Water	NMT 1.0 % w/w	0.40

Top-Quality Dextrose Anhydrous for Pharmaceuticals

Our Dextrose Anhydrous Pharma IP is precision-manufactured to meet stringent Indian Pharmacopoeia specifications. With assured solubility, low moisture, and high purity, it integrates seamlessly into injectable and oral drug preparations. Reliable distribution and export services are available, ensuring prompt supply throughout India.

Optimized for Pharmaceutical Applications

Ideal for use in pharmaceutical formulations, Dextrose Anhydrous is a trusted ingredient for energy delivery in injectables, as well as various oral preparations. Its consistent quality and controlled moisture content guarantee stability for sensitive medical uses.

FAQs of Dextrose Anhydrous Pharma IP:

Q: How is Dextrose Anhydrous Pharma IP commonly used in pharmaceutical formulations?

A: Dextrose Anhydrous Pharma IP is frequently incorporated into injectables and oral preparations to provide a reliable energy source and to stabilize active ingredients in various pharmaceutical products.

Q: What makes this grade of Dextrose Anhydrous suitable for medical and injectable applications?

A: Its compliance with Indian Pharmacopoeia standards, high purity of at least 99.5%, and low moisture content (below 0.5%) ensure safety, solubility, and stability required for medical and injectable drugs.

Q: Where should Dextrose Anhydrous Pharma IP be stored to maintain its quality?

A: It is best stored in a cool, dry place away from direct sunlight to prevent moisture absorption and maintain its crystalline integrity.

Q: What is the recommended process for dissolving Dextrose Anhydrous in pharmaceutical formulations?

A: Dextrose Anhydrous is freely soluble in water. For precise formulations, measure the required quantity and dissolve in water at ambient temperature under controlled conditions.

Q: When should pharmaceutical manufacturers opt for the IP grade of Dextrose Anhydrous?

A: Manufacturers should choose the IP grade when product specifications mandate strict adherence to Indian Pharmacopoeia requirements for quality, purity, and safety.

Q: What benefits does Dextrose Anhydrous Pharma IP offer over other glucose forms in pharmaceuticals?

A: It offers consistent purity, rapid solubility, and low moisture, making it ideal for sensitive medical applications where precise formulation and stability are critical.

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