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Benfotiamine API

Price 4500.0 INR/ Kilograms

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MOQ : 100 Kilograms

Benfotiamine API Specification

Loss on Drying
1.0%

EINECS No
245-018-1

Heavy Metal (%)
0.002%

Molecular Weight
467.45 g/mol

Smell
Odorless

Poisonous
Non-poisonous

Taste
Slightly bitter

Color
White to off-white

Molecular Formula
C19H23N4O6PS

Shelf Life
36 months

Storage
Store below 25C, protect from moisture and light

HS Code
29362310

Melting Point
164-166C

Ph Level
6.0-7.5 (1% w/v solution)

Structural Formula
Available on request

Solubility
Slightly soluble in water, soluble in methanol and ethanol

Particle Size
98% passes through 80 mesh

Boiling point
Not applicable (decomposes)

Medicine Name
Benfotiamine API

Chemical Name
S-benzoylthiamine O-monophosphate

CAS No
22457-89-2

Type
API (Active Pharmaceutical Ingredient)

Grade
Pharmaceutical Grade

Usage
Used in the treatment of diabetic neuropathy and other neurological disorders

Purity(%)
>99%

Appearance
White to off-white crystalline powder

Physical Form
Powder

Residual Solvent
Complies with ICH guidelines

Packaging
Double polythene bags in HDPE drums, 5kg/10kg/25kg

Identification
IR spectrum complies with reference standard

Related Substances
1.0%

Bulk Density
0.35-0.55 g/cm3

Microbial Limits
Total Count 1000 cfu/g, Yeast & Mold 100 cfu/g

Assay (by HPLC)
98.5%

Water Content
0.20% (by KF)

Specific Optical Rotation
+90 to +95

Endotoxin Level
<2.5 EU/mg

Benfotiamine API Trade Information

Minimum Order Quantity
100 Kilograms

Supply Ability
100 Kilograms Per Day

Delivery Time
7 Days

Sample Available
No

Sample Policy
Contact us for information regarding our sample policy

About Benfotiamine API

Packaging Size	25 kg
Form	Powder
Country of Origin	Made in India
Minimum Order Quantity	10 Kg

We are manufacturer and exporter of Benfotiamine API

It is used for the treatment and prevention of diabetic nephropathy and diabetes mellitus, type 2. In the last few years we have established ourselves as one of the most prominent organizations engaged in offering Benfotiamine . It is a synthetic version of thiamine, essential for many of the body

Pharmaceutical Grade Quality

Benfotiamine API is produced under strict quality controls, including an assay of 98.5% by HPLC and a purity exceeding 99%. All batches comply with ICH guidelines for residual solvents and heavy metal limits, ensuring excellent safety and efficacy. Our product undergoes thorough testing for microbial and endotoxin levels to guarantee patient safety.

Safe and Reliable Handling

This active ingredient is non-poisonous and odorless, making it safe to handle during manufacturing. Its stable crystalline form is slightly bitter in taste and designed for easy formulation. Packaged securely in double polythene bags within HDPE drums, it maintains its quality during storage and transport.

Therapeutic Application and Usage

Benfotiamine API is widely used in treating diabetic neuropathy and other neurological disorders. Its slightly water-soluble nature and favorable pH allow for formulation versatility in various pharmaceutical preparations, supporting innovative therapies for nerve-related conditions.

FAQs of Benfotiamine API:

Q: How is Benfotiamine API typically used in pharmaceutical formulations?

A: Benfotiamine API is primarily used as the key active ingredient in medications targeting diabetic neuropathy and neurological disorders. Its excellent purity, stability, and pharmaceutical grade ensure reliable performance in tablets, capsules, and other dosage forms.

Q: What benefits does Benfotiamine API offer over regular thiamine derivatives?

A: Benfotiamine exhibits superior bioavailability and stability compared to standard thiamine. This leads to enhanced absorption and efficacy in treating nerve-related conditions, making it a preferred choice for formulating advanced neurological therapies.

Q: Where is Benfotiamine API manufactured and supplied from?

A: This API is manufactured, exported, and supplied from India by reputable producers experienced in pharmaceutical ingredients. The product adheres to international standards, ensuring consistent quality for global distribution.

Q: What is the recommended storage condition for Benfotiamine API?

A: Benfotiamine API should be stored below 25C, protected from moisture and light, in its original packaging. This preserves its crystalline integrity and chemical stability for its full 36-month shelf life.

Q: How does the packaging process ensure the quality of Benfotiamine API?

A: The API is packed in double polythene bags placed inside high-grade HDPE drums, available in sizes of 5kg, 10kg, and 25kg. This robust packaging shields the product from environmental contaminants and maintains its purity during storage and transit.

Q: What quality specifications comply with international guidelines for Benfotiamine API?

A: The API conforms to strict ICH guidelines for residual solvents; has related substances 1.0%; a water content of 0.20%; and meets all criteria for microbial and endotoxin limits, ensuring it is suitable for pharmaceutical use globally.

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