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Tryptophan Impurity – L

1-(1H-indol-3-ylmethyl)-1,2,3,4-tetrahydro-9H-pyrido[3,4-b]indole-3-carboxylic acid

Chemical Name 1-(1H-indol-3-ylmethyl)-1,2,3,4-tetrahydro-9H-pyrido[3,4-b]indole-3-carboxylic acid
CAS No. 287170-99-4
Molecular Formula C21H19N3O2
Molecular Weight 345.4
Chemical Structure 1-(1H-indol-3-ylmethyl)-1,2,3,4-tetrahydro-9H-pyrido[3,4-b]indole-3-carboxylic acid Structure
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Tryptophan Impurity – L

Tryptophan Impurity – L is documented as a related substance of Tryptophan in pharmaceutical quality control, recognized under the EP monograph. Chemically, it is described as 1-(1H-indol-3-ylmethyl)-1,2,3,4-tetrahydro-9H-pyrido[3,4-b]indole-3-carboxylic acid. It has the molecular formula C21H19N3O2 and a molecular weight of 345.4 g/mol. Laboratories use this reference standard for impurity identification, method validation, and batch release testing related to Tryptophan. Available as a high-purity certified reference material suitable for HPLC, LC-MS, and other analytical techniques.

Tryptophan impurities reference standards are useful in pharmaceutical research. They are useful in product development, ANDA and DMF filing, Quality control (QC), method validation, and stability studies. It is also useful in the identification of unknown impurities and the assessment of genotoxic potential.

We are the BHAVANISH LIFE SCIENCES specializes in manufacturing and supplying of Tryptophan impurities that meet specific pharmacopeial standards (USP/EP/BP/IP) as well as process-related impurities.

This related products or Impurities are thoroughly characterized. Supplied with detailed COA & analytical data Like NMR / MASS / HPLC / GC / IR / TGA / Potency / Structure elucidation data (SER Report) meeting regulatory compliance.

BHAVANISH LIFE SCIENCES provides this compound for research and development and Analytical testing use only, and is not meant for human consumption. With product information including CAS number, molecular formula, molecular weight details.

BHAVANISH LIFE SCIENCES in providing high-quality impurity standards to support pharmaceutical companies in maintaining drug safety and efficacy.

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