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Erlotinib hydrochloride

Erlotinib hydrochloride
Erlotinib hydrochloride

Erlotinib hydrochloride Specification

  • Smell
  • Odorless
  • Taste
  • Bitter
  • Molecular Formula
  • C22H23N3O4
  • Shelf Life
  • 2 Years
  • Loss on Drying
  • 0.5%
  • Melting Point
  • 223-224C
  • Heavy Metal (%)
  • 0.001%
  • Structural Formula
  • See image structure
  • Storage
  • Store in cool, dry place; keep tightly closed
  • Molecular Weight
  • 393.44 g/mol
  • Solubility
  • Soluble in DMSO, methanol, and ethanol; insoluble in water
  • Poisonous
  • YES
  • HS Code
  • 29339900
  • Color
  • White to off-white
  • Medicine Name
  • Erlotinib
  • Chemical Name
  • Erlotinib Hydrochloride
  • CAS No
  • 183321-74-6
  • Type
  • Other
  • Grade
  • Other
  • Usage
  • Pharmaceutical Intermediate, Used in treatment of non-small cell lung cancer and pancreatic cancer
  • Purity(%)
  • 99.0
  • Appearance
  • White to off-white powder
  • Physical Form
  • Solid
 

Erlotinib hydrochloride Trade Information

  • Minimum Order Quantity
  • 1 Kilograms
  • Supply Ability
  • 2000 Kilograms Per Day
  • Delivery Time
  • 1 Days
 

About Erlotinib hydrochloride



Erlotinib hydrochloride (Erlontin) is a special and must-have antineoplastic agent, expertly crafted for elite pharmaceutical applications. As a select EGFR inhibitor, it targets unassailable cancer pathways, particularly in non-small cell lung cancer and pancreatic cancer treatments. Presented as a majestic, white to off-white powder, this solid intermediate boasts 99.0% purity and exceptional stability. Each batch complies strictly with USP/EP or custom standards, sealed meticulously to preserve integrity. Ideal for discerning manufacturers, Erlontin ensures safety by observing stringent limits on impurities, heavy metals, and solvents.

Erlotinib Hydrochloride Applications: Targeted Cancer Therapy

Erlotinib hydrochloride is predominantly used as a pharmaceutical intermediate in the preparation of advanced therapies, specifically as an EGFR inhibitor. Its elite use type is chemotherapeutic, demonstrating efficacy for patients with non-small cell lung cancer and pancreatic cancer. This special compound is vital for manufacturers developing targeted cancer medicines, and its select performance has rendered it a must-have ingredient in research and development for antineoplastic agents globally.


Supply Ability, Export, and Sample Dispatching

As an unassailable resource in the elite pharmaceutical market, Erlotinib hydrochloride is available in substantial supply. Swift dispatching from the point of arrival at the specified FOB port ensures timely delivery to domestic and export markets. Samples can be provided upon request to support evaluation and compliance. With reliable logistics and select packaging, clients are assured of product integrity from export to arrival, reinforcing trust and satisfaction.


FAQs of Erlotinib hydrochloride:


Q: How should Erlotinib hydrochloride be stored to maintain its stability?

A: Erlotinib hydrochloride should be stored in a cool, dry place, kept tightly closed, and protected from moisture. Following these recommendations preserves its stability and prolongs its shelf life up to 2 years.

Q: What are the main uses of Erlotinib hydrochloride in pharmaceuticals?

A: Erlotinib hydrochloride serves as a pharmaceutical intermediate and is primarily used in the formulation of drugs for the treatment of non-small cell lung cancer and pancreatic cancer due to its powerful EGFR-inhibiting properties.

Q: When can customers expect the arrival of dispatched Erlotinib hydrochloride orders?

A: Orders are processed with efficiency; upon completion of export formalities, dispatching occurs from the specified FOB port with prompt arrival timelines dependent on the destination and chosen shipping method.

Q: Where can I request samples or additional product specifications for Erlotinib hydrochloride?

A: Samples and detailed product specifications can be requested directly from the supplier, distributor, or manufacturer. These entities provide comprehensive support and documentation for prospective clients.

Q: What is the process for ensuring the quality and compliance of Erlotinib hydrochloride?

A: Every batch of Erlotinib hydrochloride adheres to USP/EP or custom reference standards. Stringent testing confirms total impurities (0.5%), heavy metal content (0.001%), and residual solvents comply with ICH Q3C guidelines.

Q: What benefits does using Erlotinib hydrochloride with high purity and low impurity levels provide?

A: High purity (99.0%) and low impurity levels ensure potent therapeutic effects, minimize the risk of side effects, and support compliance with regulatory guidelines, making Erlotinib hydrochloride a preferred choice for elite pharmaceutical manufacturing.

Price 100 INR/ Kilograms

  • Minimum Order Quantity
  • 1 Kilograms
  • Supply Ability
  • 2000 Kilograms Per Day
  • Delivery Time
  • 1 Days
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"We are into Supply of Pharmaceutical Raw Material / API". We only deal in Bulk Quantity. We do not deals in Pakistan and Bangladesh Countries.