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Acyclovir EP Impurity L

Acyclovir EP Impurity L

100 INR/Number
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Product Details:

  • Smell Odorless
  • Usage Reference standard, impurity profiling
  • Grade Pharma Grade
  • Molecular Formula C8H10N5O3
  • Properties High purity, suitable for pharmaceutical synthesis, stable compound
  • Poisonous NO
  • Product Type Pharmaceutical Raw Material
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Acyclovir EP Impurity L Price And Quantity

  • 100 INR/Number
  • 1 Number

Acyclovir EP Impurity L Product Specifications

  • Odorless
  • Reference standard, impurity profiling
  • For laboratory research and pharmaceutical analysis
  • Pharma Grade
  • White to off-white powder
  • 2 years
  • C8H10N5O3
  • High purity, suitable for pharmaceutical synthesis, stable compound
  • NO
  • Pharmaceutical Raw Material
  • Powder
  • 29339900
  • 223.20 g/mol
  • Soluble in DMSO, slightly soluble in water
  • >98%
  • 102111-40-2
  • Available upon request
  • Crystalline
  • Store at 2-8C, protected from light and moisture
  • Acyclovir Derivative

Product Description



Secure the ace choice for your research with Acyclovir EP Impurity L (Synonym: 9-((2-hydroxyethoxy)methyl)guanine impurity L), now available at an unbeatable price. This impurity reference standard is scarce in supply and offers pharma-grade, >98% purity-a truly unassailable offer for laboratories and pharmaceutical synthesis. Delivered as a crystalline, odorless, white to off-white powder, each sealed vial is shipped under inert atmosphere to ensure stability and safety. Enjoy astounding advantages like reliable identity confirmation (HPLC, NMR, MS), a 2-year shelf life, and prompt drop-off within 2 weeks of order.

Key Features and Application Areas of Acyclovir EP Impurity L

Acyclovir EP Impurity L is primarily used as a reference standard for impurity profiling and quality management in pharmaceutical research. This high-purity, pharma-grade compound is suitable for laboratory analysis and synthesis applications. It is stable, crystalline, and soluble in DMSO, supporting reliable results throughout different research processes. The impurity is packaged under strict conditions to maintain its integrity, ensuring optimal performance in pharmaceutical labs and research institutions.


Export Markets, Supply, and Shipped Goods Handling

Acyclovir EP Impurity L is supplied globally, with main export markets spanning Asia, Europe, and North America. Shipped goods originate from our India FOB port, allowing efficient worldwide drop-off. We maintain a robust supply ability to meet high proposal amounts and ensure delivery within two weeks of confirmed orders. All products are carefully packed and transported under ambient conditions, safeguarding the uncompromising quality and stability required for pharmaceutically critical shipments.


FAQ's of Acyclovir EP Impurity L:


Q: How should Acyclovir EP Impurity L be stored to maintain its quality?

A: Acyclovir EP Impurity L should be stored at 2-8C, protected from light and moisture, to ensure long-term stability and preserve purity.

Q: What identification methods are used to confirm the identity of Acyclovir EP Impurity L?

A: The compound's identity is confirmed using advanced techniques such as HPLC (High Performance Liquid Chromatography), NMR (Nuclear Magnetic Resonance), and MS (Mass Spectrometry).

Q: When is the estimated lead time for delivery after placing an order?

A: Orders for Acyclovir EP Impurity L are typically processed and shipped within two weeks of order confirmation.

Q: Where is Acyclovir EP Impurity L commonly applied?

A: This impurity is primarily used in laboratories for pharmaceutical research, particularly as a reference standard for impurity profiling and for pharmaceutical analysis.

Q: What benefits does the high purity of this product offer researchers?

A: With over 98% purity, the product ensures highly accurate analytical results, supporting stringent pharmaceutical quality control and research applications.

Q: How should Acyclovir EP Impurity L be handled during laboratory use?

A: Although non-hazardous, it is recommended to use gloves and safety glasses when handling the compound to maintain safety and product integrity.

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    NATIONAL ANALYTICAL CORPORATION - CHEMICAL DIVISION
    GST : 27AWSPS9814L1ZF
  • Kesarkunj, Rm No. 9, Vasanji Lalji Road, Kandivali (W), Mumbai - 400067, Maharashtra, India
  • Phone : 08071630254
  • Mr Nilesh Shah (Director)
  • Mobile : 08071630254
  • Mr Dharmik Shah
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