Determine the necessary mass, volume, or concentration for preparing a solution.
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≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature Ships Normal Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 2 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Indinavir is a member of the novel hydroxyaminopentane amide class of HIV-1 protease inhibitors.
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organic acids and derivatives |
| Classe | Carboxylic acids and derivatives |
| Subclass | Amino acids, peptides, and analogues |
| Intermediate Tree Nodes | Amino acids and derivatives - Alpha amino acids and derivatives |
| Direct Parent | Alpha amino acid amides |
| Alternative Parents | Indanes Piperazine carboxamides Aralkylamines N-alkylpiperazines Benzene and substituted derivatives N-acyl amines Pyridines and derivatives Heteroaromatic compounds Secondary alcohols Trialkylamines Secondary carboxylic acid amides 1,2-aminoalcohols Azacyclic compounds Hydrocarbon derivatives Carbonyl compounds Organic oxides Organopnictogen compounds |
| Molecular Framework | Aromatic heteropolycyclic compounds |
| Substituents | Alpha-amino acid amide - Indane - Piperazine-2-carboxamide - N-alkylpiperazine - Aralkylamine - Monocyclic benzene moiety - 1,4-diazinane - Fatty amide - N-acyl-amine - Piperazine - Pyridine - Benzenoid - Fatty acyl - Heteroaromatic compound - Tertiary amine - Secondary carboxylic acid amide - Secondary alcohol - 1,2-aminoalcohol - Carboxamide group - Tertiary aliphatic amine - Azacycle - Organoheterocyclic compound - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Alcohol - Amine - Organic oxide - Carbonyl group - Organonitrogen compound - Hydrocarbon derivative - Organooxygen compound - Aromatic heteropolycyclic compound |
| Description | This compound belongs to the class of organic compounds known as alpha amino acid amides. These are amide derivatives of alpha amino acids. |
| External Descriptors | dicarboxylic acid diamide - N-(2-hydroxyethyl)piperazine - piperazinecarboxamide |
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| Solubilité | Soluble in water (0.02 mg/mL).(unbuffered) |
|---|---|
| Indice de réfraction | n20D1.64 |
| Rotation spécifique [α] | α20/D +24.1°, c = 0.01 in chloroform |
| Point d'ébullition (°C) | 877.89° C at 760 mmHg |
| Point de fusion (°C) | 153-154° C |
| Poids moléculaire | 613.800 g/mol |
| XLogP3 | 2.800 |
| Hydrogen Bond Donor Count | 4 |
| Hydrogen Bond Acceptor Count | 7 |
| Rotatable Bond Count | 12 |
| Exact Mass | 613.363 Da |
| Monoisotopic Mass | 613.363 Da |
| Topological Polar Surface Area | 118.000 Ų |
| Heavy Atom Count | 45 |
| Formal Charge | 0 |
| Complexity | 952.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 5 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |