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Amino Iso G. Acid
Amino Iso G. Acid

Amino Iso G. Acid

Amino Iso G. Acid Specification

  • Taste
  • Slightly bitter
  • Smell
  • Odorless
  • Shelf Life
  • 24 months
  • Boiling point
  • Decomposes
  • Water Resistant
  • Yes
  • Poisonous
  • Yes
  • Solvent Color
  • Colorless in solution
  • Density
  • 1.15 Gram per cubic centimeter(g/cm3)
  • Resistance
  • Chemically stable under normal conditions
  • Rubbing Resistance
  • Good
  • Solubility
  • Soluble in water
  • Shape
  • Crystalline
  • Molecular Formula
  • C5H11NO2
  • Moisture (%)
  • 1.0%
  • Chemical Name
  • Aminoiso G. Acid
  • Type
  • Amino Acid
  • Usage
  • Industrial
  • Purity(%)
  • 98%
  • Application
  • Pharmaceutical Intermediate
  • Appearance
  • White crystalline powder
  • Physical Form
  • Solid
  • Grade
  • Technical Grade
 
 

About Amino Iso G. Acid

Amino Iso G. Acid

CAS NO. : 50976-35-7

  • M.W. : 303
  • Empirical Formula : C10H9S2O6N
  • Synonyms : 2 - Naphthylamine 5 : 7 Disulfonic Acid
  • Form Supplied : Wet Cake
  • Basis For Sale : On Real Content, M.W. 303
  • Packing : 25/50 Kgs. HDPE. Bags with inside Polythene Liner.
Technical Data
  • Description : Yellow Powder
  • Nature of Material : Free Sulphonic Acid.
  • Strength : @ 70%
  • Solubility : Soluble In Water
  • Use : Intermediate For Dye stuffs.


High-Purity Composition for Pharmaceutical Use

Amino Iso G. Acid meets stringent purity requirements, making it an excellent choice for use as a pharmaceutical intermediate. Its technical grade and 98% purity ensure reliable performance in the synthesis of complex drug compounds. The products chemically stable and water-soluble nature enhances its versatility and effectiveness in various industrial processes.


Versatile Industrial Applications

Thanks to its robust chemical resistance and moisture resistance, Amino Iso G. Acid can be integrated easily into diverse industrial applications. As a white crystalline powder, it mixes easily in formulations and provides consistent, high-quality results. Its odorless and non-poisonous properties make it safe to handle in controlled environments.

FAQs of Amino Iso G. Acid:


Q: How is Amino Iso G. Acid commonly used in the pharmaceutical industry?

A: Amino Iso G. Acid serves predominantly as a pharmaceutical intermediate, meaning it is a key component in the synthesis of various medicinal compounds. Its high purity and stability make it suitable for producing active ingredients in pharmaceutical manufacturing processes.

Q: What are the notable physical properties of Amino Iso G. Acid?

A: The compound appears as a white, crystalline, odorless solid with a slightly bitter taste, features a density of 1.15 g/cm, and dissolves readily in water. It is chemically stable under normal conditions, colorless when dissolved, and maintains its integrity for up to 24 months if stored properly.

Q: When should Amino Iso G. Acid be utilized in a manufacturing process?

A: Amino Iso G. Acid should be incorporated during the intermediate stages of pharmaceutical compound synthesis, especially when a high-purity, chemically stable amino acid is required to ensure efficacy and reliability in the final product.

Q: Where is Amino Iso G. Acid produced and available for supply?

A: This amino acid is produced, distributed, and supplied by manufacturers, exporters, importers, and traders throughout India. It is available to industrial users requiring technical-grade amino acids for pharmaceutical applications.

Q: What is the process for ensuring the quality and stability of Amino Iso G. Acid?

A: To preserve purity (98%) and effectiveness, Amino Iso G. Acid is manufactured under controlled conditions, tested for moisture (1.0%), and packaged in a way that prevents contamination or decomposition. Proper storage extends the shelf life up to 24 months.

Q: How does using Amino Iso G. Acid benefit pharmaceutical production?

A: Its high purity, chemical stability, and good solubility make Amino Iso G. Acid an optimal choice for pharmaceutical intermediates, supporting efficient synthesis and quality assurance in drug development while minimizing the risk of impurities.

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