Divalproex Active Pharmaceutical Ingredients

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Divalproex Active Pharmaceutical Ingredients

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MOQ : 25 Kilograms

Divalproex Active Pharmaceutical Ingredients Specification

Shelf Life
36 months

Loss on Drying
0.5%

Poisonous
No (when used as directed)

Heavy Metal (%)
0.001%

Boiling point
Not applicable (decomposes before boiling)

EINECS No
278-304-8

Storage
Store in a cool, dry, and well-ventilated place away from light

Particle Size
90% < 250 m

Molecular Weight
310.41 g/mol

Melting Point
120-124C

Ph Level
7.0 - 8.5 (1% solution)

HS Code
29420090

Taste
Characteristic

Structural Formula
(Image-based, refer chemical structure)

Solubility
Freely soluble in water

Smell
Odorless

Molecular Formula
C16H31NaO4

Color
White to off-white

Medicine Name
Divalproex

Chemical Name
Divalproex Sodium

CAS No
76584-70-8

Type
Active Pharmaceutical Ingredient (API)

Grade
Pharmaceutical Grade

Usage
Used for the treatment of epilepsy, bipolar disorder, and migraine prophylaxis

Purity(%)
>99%

Appearance
White to off-white crystalline powder

Physical Form
Solid

Compatibility
Compatible with common excipients used in formulation

Bacterial Endotoxins
< 0.5 IU/mg

Microbial Limits
Total aerobic microbial count: 100 cfu/g; Total yeast and mould count: 10 cfu/g

Stability
Stable under recommended storage conditions

Regulatory Status
USDMF/EDMF available

Related Substances
0.1%

Identification
By IR, complies with standard

Residual Solvents
Complies with ICH Q3C guidelines

Assay (by HPLC)
>99.0%

Shelf Condition
Tightly closed containers at room temperature (15-30C)

Packaging
25 kg HDPE drum or as per customer requirement

Impurities
Complies with pharmacopeial standards

Divalproex Active Pharmaceutical Ingredients Trade Information

Minimum Order Quantity
25 Kilograms

Payment Terms
Cash in Advance (CID), Cash Against Delivery (CAD), Cash on Delivery (COD)

Supply Ability
500 Kilograms Per Month

Delivery Time
5-7 Days

Main Export Market(s)
Asia, Australia, Central America, North America, South America, Eastern Europe, Western Europe, Middle East, Africa

Main Domestic Market
All India

About Divalproex Active Pharmaceutical Ingredients

Discover the ephemeral yet inestimable value of our Divalproex Active Pharmaceutical Ingredient (API), distinguished by unrivaled purity at >99% and immaculate compliance with global pharmacopeial standards. Affordable and meticulously crafted, this API features minimal related substances (0.1%) and stringent control of residual solvents. Each batch guarantees regulatory transparency (USDMF/EDMF available), bacterial endotoxins <0.5 IU/mg, and compatibility with common excipients. Supplied in robust, secure 25 kg HDPE drums, Divalproex offers stability and efficacy-your optimal choice for innovative epilepsy, bipolar disorder, and migraine formulations. Shop now for excellence you can trust.

Competitive Advantages and Specific Uses of Divalproex API

Divalproex API boasts competitive advantages, including a high assay value (>99.0%), exceptional microbial purity, and inestimable regulatory credentials. It is specifically used for the synthesis of formulations aimed at treating epilepsy, bipolar disorder, and migraine prophylaxis. The direction of use involves precise blending with compatible excipients, following standard pharmaceutical protocols. General use in pharmaceutical manufacturing requires its integration into dosage forms such as tablets and capsules, supporting consistent therapeutic outcomes and unrivaled product efficacy.

FOB Port, Export Markets, and Sample Policy for Divalproex API

Our impeccable Divalproex API packaging ensures product integrity from the moment of dispatch. Shipments are available FOB from major Indian ports, maximizing affordability and reducing unnecessary expenditure. We serve comprehensive export markets, notably across Asia, Europe, and North America. Samples are provided under a clear charge policy that offsets preparation and handling expenses. Every effort is made to deliver timely and secure shipments, maintaining our reputation as a trusted exporter and supplier within the pharmaceutical industry.

FAQ's of Divalproex Active Pharmaceutical Ingredients:

Q: How is Divalproex Active Pharmaceutical Ingredient identified and what measures ensure its purity?

A: Divalproex API is identified by infrared spectroscopy (IR) and complies with pharmacopeial standards, ensuring unrivaled purity validated by high-performance liquid chromatography (HPLC) with an assay above 99%.

Q: What specific uses does Divalproex API serve in medical formulations?

A: Divalproex API is primarily used in pharmaceutical preparations for the treatment of epilepsy, bipolar disorder, and for migraine prophylaxis, offering consistent efficacy in solid oral dosage forms such as tablets and capsules.

Q: Where is your Divalproex API exported, and what packaging options are available?

A: Our Divalproex API is exported globally, with main export markets across Asia, Europe, and North America. Packaging options include standard 25 kg HDPE drums or customized packaging per customer request, ensuring product safety and integrity.

Q: What is the process for ordering samples of Divalproex API and are there associated charges?

A: Samples are available upon request, and a nominal charge is applied to cover packaging and handling expenditures. Interested parties can contact our sales team for sample submission and shipment details.

Q: What are the storage conditions and shelf life of Divalproex API?

A: Divalproex API should be stored in tightly closed containers at room temperature (15-30C), away from light and moisture. It maintains stability under these conditions with a shelf life of 36 months.

Q: How does Divalproex API ensure compatibility with other pharmaceutical excipients?

A: Our Divalproex API is carefully tested to confirm compatibility with common excipients used in various formulations, supporting efficient and safe product development at every stage of pharmaceutical manufacturing.

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