≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at -20°C Ships Ice chest + Ice pads 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 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Product Describtion:
Biocytin is a conjugate of D-biotin and L-lysine, where the carboxylate of D-biotin is coupled with the ϵ-amine of L-lysine via a secondary amide bond. Biocytin is a classical neuroanatomical tracer commonly used to map brain connectivity. Biocytin is used as a versatile marker in anterograde, retrograde and intracellular neuroanatomical investigations and in biotinidase assays
| Pubchem Sid | 504755729 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504755729 |
| Sorrisi canonici | C1C2C(C(S1)CCCCC(=O)NCCCCC(C(=O)O)N)NC(=O)N2 |
| IUPAC Name | (2S)-6-[5-[(3aS,4S,6aR)-2-oxo-1,3,3a,4,6,6a-hexahydrothieno[3,4-d]imidazol-4-yl]pentanoylamino]-2-aminohexanoic acid |
| InChIKey | BAQMYDQNMFBZNA-MNXVOIDGSA-N |
| INCHI | 1S/C16H28N4O4S/c17-10(15(22)23)5-3-4-8-18-13(21)7-2-1-6-12-14-11(9-25-12)19-16(24)20-14/h10-12,14H,1-9,17H2,(H,18,21)(H,22,23)(H2,19,20,24)/t10-,11-,12-,14-/m0/s1 |
| Isomeri SMILES | C1[C@H]2[C@@H]([C@@H](S1)CCCCC(=O)NCCCC[C@@H](C(=O)O)N)NC(=O)N2 |
| Peso molecolare | 372.483 |
| Beilstein | 97197 |
| Reaxy-Rn | 1092147 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1092147&ln= |
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 - Alpha amino acids |
| Direct Parent | L-alpha-amino acids |
| Alternative Parents | Imidazolyl carboxylic acids and derivatives Medium-chain fatty acids Heterocyclic fatty acids Thiolanes Imidazolines Amino acids Isoureas Propargyl-type 1,3-dipolar organic compounds Azacyclic compounds Carboximidamides Carboxylic acids Dialkylthioethers Monocarboxylic acids and derivatives Organopnictogen compounds Hydrocarbon derivatives Organic oxides Carbonyl compounds Monoalkylamines |
| Molecular Framework | Aliphatic heteropolycyclic compounds |
| Substituents | L-alpha-amino acid - Imidazolyl carboxylic acid derivative - Medium-chain fatty acid - Heterocyclic fatty acid - Fatty acid - Fatty acyl - Thiolane - 2-imidazoline - Amino acid - Isourea - Azacycle - Carboximidic acid - Carboximidic acid derivative - Organoheterocyclic compound - Dialkylthioether - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Carboximidamide - Carboxylic acid - Thioether - Monocarboxylic acid or derivatives - Organic oxide - Organonitrogen compound - Primary aliphatic amine - Organooxygen compound - Organic oxygen compound - Primary amine - Organic nitrogen compound - Organopnictogen compound - Amine - Carbonyl group - Hydrocarbon derivative - Aliphatic heteropolycyclic compound |
| Descrizione | This compound belongs to the class of organic compounds known as l-alpha-amino acids. These are alpha amino acids which have the L-configuration of the alpha-carbon atom. |
| External Descriptors | azabicycloalkane - ureas - thiabicycloalkane - monocarboxylic acid amide - non-proteinogenic L-alpha-amino acid - L-lysine derivative |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Data | Oggetto |
|---|---|---|---|
 J2211789 | Certificate of Analysis | Apr 03, 2026 | B131254 |
| J2211790 | Certificate of Analysis | Apr 03, 2026 | B131254 |
| J2211791 | Certificate of Analysis | Apr 03, 2026 | B131254 |
| J2211829 | Certificate of Analysis | Apr 03, 2026 | B131254 |
| J2211864 | Certificate of Analysis | Apr 03, 2026 | B131254 |
| Solubilità | Solvent:water, Max Conc. mg/mL: 18.62, Max Conc. mM: 50 with gentle warming |
|---|---|
| Indice di rifrazione | [α]20/D +53°, c = 1.05% in 0.1 M NaOH |
| Punto di fusione (°C) | ~245 °C |
| Peso molecolare | 372.500 g/mol |
| XLogP3 | -2.400 |
| Hydrogen Bond Donor Count | 5 |
| Hydrogen Bond Acceptor Count | 6 |
| Rotatable Bond Count | 11 |
| Exact Mass | 372.183 Da |
| Monoisotopic Mass | 372.183 Da |
| Topological Polar Surface Area | 159.000 Ų |
| Heavy Atom Count | 25 |
| Formal Charge | 0 |
| Complexity | 491.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 4 |
| 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 |
