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Atenolol IP API with DMF

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MOQ : 100 Kilograms

Atenolol IP API with DMF Specification

Poisonous
Non-poisonous under normal use

EINECS No
249-028-2

Loss on Drying
NMT 0.5%

Melting Point
152-155C

Shelf Life
5 Years

Structural Formula
C14H22N2O3

Molecular Formula
C14H22N2O3

Solubility
Freely soluble in water, sparingly soluble in ethanol

Particle Size
D90 < 150 microns

Storage
Store in a cool, dry place in tightly closed containers

Heavy Metal (%)
Not more than 20 ppm

Molecular Weight
266.34 g/mol

Smell
Odorless

HS Code
29420090

Color
White

Taste
Bitter

Ph Level
6.0-7.5 (1% solution in water)

Medicine Name
Atenolol IP API with DMF

Chemical Name
4-(2-Hydroxy-3-[(1-methylethyl)amino]propoxy)benzeneacetamide

CAS No
29122-68-7

Type
Active Pharmaceutical Ingredient

Grade
IP (Indian Pharmacopoeia)

Usage
Used in the manufacturing of antihypertensive drugs

Purity(%)
>99%

Appearance
White or almost white crystalline powder

Physical Form
Solid

Endotoxin Level
NMT 0.5 EU/mg

Microbial Limit
Complies with IP limits

DMF Status
Drug Master File (DMF) available

Packaging
HDPE/LDPE bags with outer drum

Residue on Ignition
NMT 0.1%

Related Substances
Single impurity NMT 0.5%, total impurities NMT 1.0%

Regulatory Compliance
Certified as per Indian Pharmacopoeia (IP), available with DMF

Identification
Complies with IP standards (IR and HPLC)

Atenolol IP API with DMF Trade Information

Minimum Order Quantity
100 Kilograms

Supply Ability
1000 Kilograms Per Month

Delivery Time
7 Days

Atenolol IP API with DMF About

Purchase the masterful Atenolol IP API with DMF, highlighted for its splendid compliance with Indian Pharmacopoeia (IP) standards. Personalise your pharmaceutical supply with this soaring quality active ingredient-purity exceeding 99%, residue on ignition not more than 0.1%, and a superb particle size (D90 < 150 microns). Offered as an odorless, bitter, white crystalline powder, it's non-poisonous under normal use and designed for reliable hypertensive drug production. Secure Packaging: HDPE/LDPE bags with outer drum. DMF available for regulatory needs. Trusted by importers, exporters, and manufacturers worldwide from India.

Atenolol IP API with DMF: Features and Usage

This splendid Atenolol IP API is widely used in the manufacturing of antihypertensive medicines, with seamless compatibility across diverse formulation media. Its application is straightforward-simply integrate into your established production process following standard operating protocols. Key material features include high purity, strict impurity controls, and outstanding solubility in water. Designed for pharmaceutical excellence, it supports robust therapeutic outcomes while ensuring compliance with all IP guidelines and stringent regulatory standards.

Sample Policy, Supply, and Delivery Information

We support potential buyers by offering samples at a fair asking price, allowing hands-on assessment before large-scale purchase. Supply ability for Atenolol IP API with DMF is soaring, ensuring seamless availability to meet your manufacturing needs. Orders are delivered with quick dispatch, typically within a few days of order confirmation. Our team is committed to efficient, dependable service, optimizing the delivery process for clients worldwide seeking excellence in pharmaceutical ingredients.

FAQ's of Atenolol IP API with DMF:

Q: How should Atenolol IP API with DMF be stored to maintain its quality?

A: This product should be stored in a cool, dry place within tightly closed containers to preserve its purity and extend its 5-year shelf life.

Q: What are the highlighted regulatory compliance features of this API?

A: Atenolol IP API with DMF is fully certified according to Indian Pharmacopoeia standards, accompanied by a Drug Master File (DMF) for streamlined regulatory submissions.

Q: When can I expect delivery after placing an order?

A: Quick dispatch is a priority, and orders are usually delivered within a few days from order confirmation, based on your location and supply needs.

Q: Where can samples of Atenolol IP API with DMF be obtained?

A: Samples are available upon request at the asking price, enabling evaluation before full-scale procurement.

Q: What is the benefit of using Atenolol IP API with DMF in pharmaceutical manufacturing?

A: Its masterful purity levels, compliance with IP standards, and availability of DMF documentation benefit both quality assurance and regulatory approvals, supporting splendid therapeutic product development.

Q: How is Atenolol IP API typically used in medicine production?

A: It is utilized as an active ingredient in antihypertensive drug formulations, easily integrated due to its high solubility and controlled particle size.

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