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Etamsylate

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MOQ : 50 Kilograms

Etamsylate Specification

Shelf Life
5 years if properly stored

Poisonous
Non-poisonous

Storage
Store below 25C, dry and protected from light

Smell
Odorless

Taste
Slightly bitter

Color
White

Solubility
Freely soluble in water, very slightly soluble in ethanol and chloroform

Heavy Metal (%)
0.001%

Particle Size
80 mesh (typical)

Ph Level
6.0-7.5 (1% aqueous solution)

Molecular Formula
C10H17NO5S

Molecular Weight
263.31 g/mol

Boiling point
Not applicable (decomposes)

HS Code
29221990

Melting Point
166-170C

Structural Formula
C10H17NO5S (refer image for graphical structure)

EINECS No
220-089-7

Loss on Drying
0.5%

Medicine Name
Etamsylate

Chemical Name
2,5-Dihydroxybenzenesulfonic acid monoethanolamine salt

CAS No
2624-44-4

Type
Active Pharmaceutical Ingredient (API)

Grade
Pharmaceutical Grade

Usage
Used as a haemostatic agent to prevent and control bleeding

Purity(%)
99%

Appearance
White to almost white crystalline powder

Physical Form
Powder

Sulphated Ash
0.1%

Specific Optical Rotation
+67 to +71 (c=2 in water)

Chloride Content
0.05%

Bacterial Endotoxins
<0.5 IU/mg

Identification
Complies with standard tests (IR, UV)

Packing
Fibre drum with double polyethylene bags, 25 kg net

Residual Solvent
Complies as per ICH guidelines

Etamsylate Trade Information

Minimum Order Quantity
50 Kilograms

Supply Ability
50 Kilograms Per Week

Delivery Time
1 Week

About Etamsylate

The Ethamsylate is used as the effective medicine, suited for the treatment of bleeding. Its utilization can reduce the bleeding and can deal with the abnormal blood loss. Also, this is useful in the dysfunctional uterine bleeding. Ethamsylate has been made to provide effectiveness in the several conditions of bleeding. It must be taken under a professional administration only. Offered is a haemostatic agent, formulated for the management of blood loss caused by surgery as well as menorrhagia.

Reliable Haemostatic Solution

Etamsylate is widely recognized for its effectiveness in managing and reducing bleeding. It works by promoting stable blood clot formation, making it a preferred choice in various clinical and surgical settings. Its consistent quality and compliance with international pharmaceutical standards guarantee safety and efficacy each time it is used.

Stringent Quality & Safety Measures

Manufactured following rigorous protocols, Etamsylate meets pharmaceutical-grade criteria. It boasts a high purity level (99%), minimal impurities, and strict adherence to specifications regarding chloride content, bacterial endotoxins, and heavy metals. These controls ensure the ingredient is safe for medicinal use and long-term storage, backed by a five-year shelf life.

Convenient Packaging and Storage

To preserve Etamsylates integrity, it is packed securely in fibre drums with double polyethylene bags. This packaging protects the powder from moisture and light, supporting its stability during storage and transportation. For optimal shelf life and performance, it should be stored below 25C in a dry, protected environment.

FAQs of Etamsylate:

Q: How is Etamsylate typically used in medical applications?

A: Etamsylate is primarily used as a haemostatic agent to control and prevent bleeding. It is administered in medical and surgical scenarios to support hemostasis, often as part of formulations designed for intravenous or oral use.

Q: What are the main benefits of using Etamsylate as an API?

A: Etamsylate offers rapid, reliable bleeding control with high purity and low toxicity. Its excellent solubility in water ensures ease of formulation, while stringent quality standards make it a trusted choice for pharmaceutical manufacturers.

Q: What is the recommended storage condition for Etamsylate powder?

A: Etamsylate should be stored below 25C in a dry, protected environment away from direct light. Proper storage maximizes its shelf life, which is five years under recommended conditions.

Q: What quality tests does Etamsylate comply with before distribution?

A: Etamsylate is verified through identification tests (IR, UV), and adheres to strict limits for chloride content, sulphated ash, and heavy metals. It also complies with ICH guidelines for residual solvents and tests negative for excessive bacterial endotoxins.

Q: Where does Etamsylate fall under in terms of regulatory classification?

A: Etamsylate is classified as a pharmaceutical grade Active Pharmaceutical Ingredient (API), suitable for human medicinal use according to international standards.

Q: What packaging is used for safe transport and storage of Etamsylate?

A: Etamsylate is securely packed in fibre drums with double polyethylene bags, each containing a net weight of 25 kg. This packaging protects the integrity of the powder from environmental factors during transit and storage.

Q: What is the chemical composition of Etamsylate?

A: Etamsylates molecular formula is C10H17NO5S, and it is known chemically as 2,5-Dihydroxybenzenesulfonic acid monoethanolamine salt. It is provided as a white, odorless, slightly bitter powder with a typical particle size of 80 mesh.

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