Tryptophol - ≥97%(GC) , CAS No.526-55-6

CAS: 526-55-6 Cat. No.: T112368 Fórmula: C10H11NO Peso molecular: 161.2 Beilstein Registry Number: 125553 Número CE: 208-393-2 PubChem CID: 10685
Disponível para encomenda
GRADE & PURITY ≥97%(GC)
Synonyms
EINECS 208-393-2 | SB14961 | Z1123806416 | FT-0600657 | ISUPSL100239 | Q5479351 | 1H-Indolyl-3-ethanol | AC-3286 | ETHANOL, 3-INDOLYL- | TRYPTOPHOL [MI] | WLN: T56 BMJ D2Q | CCG-266289 | DTXSID2060173 | Ethanol, 2-indol-3-yl- | 2-(3-INDOLE)ETHANOL | 3-.BE
Storage
Desiccated,Room temperature
Shipped In
Normal
★
Size
Alemanha (EU)
USA*
Price
Qty
1g
T112368-1g
—
1 Em stock

8,59€

12,93€
Gravar 4,34 € (33.56%)
5g
T112368-5g
—
2 Em stock

18,14€

27,68€
Gravar 9,55 € (34.48%)
25g
T112368-25g
—
1 Em stock

61,52€

92,76€
Gravar 31,24 € (33.68%)
100g
T112368-100g
—
1 Em stock

242,88€

364,36€
Gravar 121,48 € (33.34%)
Enter a quantity for the sizes you want to add.
🧪

Why this grade

≥97%(GC) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Desiccated,Room temperature Ships Normal Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 2 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Visão geral

Reactant for preparation of Inhibitors of the C-terminal domain of RNA polymerase II and their antitumor activities,Anti-HIV-1 agents, Inhibitors of Protein-Protein Interactions,Partial agonists of the serotonin 5-HT1A receptor,Growth hormone secretagogues,Vascular endothelial growth factor (VEGF) inhibitors,A2B adenosine receptor ligands, Potential detoxification inhibitors of the crucifer phytoalexin brassinin, Inhibitors of interleukine 6,Dual binding site acetylcholinesterase inhibitors.

Specifications

Sinónimos
EINECS 208-393-2 | SB14961 | Z1123806416 | FT-0600657 | ISUPSL100239 | Q5479351 | 1H-Indolyl-3-ethanol | AC-3286 | ETHANOL, 3-INDOLYL- | TRYPTOPHOL [MI] | WLN: T56 BMJ D2Q | CCG-266289 | DTXSID2060173 | Ethanol, 2-indol-3-yl- | 2-(3-INDOLE)ETHANOL | 3-.BE
Especificações e pureza
≥97%(GC)
Condições de armazenamento de armazenamento
Desiccated,Room temperature
Enviado em
Normal
Pureza
≥97%(GC)
Nomes e identificadores
Pubchem Sid504751985
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504751985
Sorrisos canónicosC1=CC=C2C(=C1)C(=CN2)CCO
IUPAC Name2-(1H-indol-3-yl)ethanol
InChIKeyMBBOMCVGYCRMEA-UHFFFAOYSA-N
INCHI1S/C10H11NO/c12-6-5-8-7-11-10-4-2-1-3-9(8)10/h1-4,7,11-12H,5-6H2
SMILES isoméricas C1=CC=C2C(=C1)C(=CN2)CCO
WGK Alemanha 3
RTECS KL3685000
PubChem CID 10685
Peso molecular 161.2
Beilstein 125553
Reaxy-Rn 125553

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
ClasseIndoles and derivatives
SubclassIndoles
Intermediate Tree Nodes Not available
Direct Parent3-alkylindoles
Alternative Parents Substituted pyrroles  Benzenoids  Heteroaromatic compounds  Azacyclic compounds  Primary alcohols  Organopnictogen compounds  Organonitrogen compounds  Hydrocarbon derivatives  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents 3-alkylindole - Benzenoid - Substituted pyrrole - Heteroaromatic compound - Pyrrole - Azacycle - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Primary alcohol - Organooxygen compound - Organonitrogen compound - Alcohol - Aromatic heteropolycyclic compound
DescriçãoThis compound belongs to the class of organic compounds known as 3-alkylindoles. These are compounds containing an indole moiety that carries an alkyl chain at the 3-position.
External Descriptors a small molecule
Estrutura 3D
Modelo de Estrutura Química Interativa





Alvos associados (humanos)
GLP1R Tclin Glucagon-like peptide 1 receptor (111429 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SH-SY5Y (11521 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
U-251 (51189 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HaCaT (4069 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NTRK2 Tclin Neurotrophic tyrosine kinase receptor type 2 (3279 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
BRCA1 Tchem Breast cancer type 1 susceptibility protein (15908 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Alvos associados (não humanos)
Plenodomus lingam (178 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Plasmodium falciparum (966862 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
N2a (708 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Rhizoctonia solani (2251 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Laetisaria fuciformis (2 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Cryphonectria parasitica (24 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Magnaporthiopsis poae (2 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mecanismos de ação
Certificados(CoA,COO,BSE/TSE e Mapa de Análise)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

12 results found

Lot NumberCertificate TypeDataItem
F2421342Certificate of AnalysisApr 01, 2024 T112368
C2618248Certificate of AnalysisSep 04, 2023 T112368
H2422109Certificate of AnalysisSep 04, 2023 T112368
H2422111Certificate of AnalysisSep 04, 2023 T112368
I2312668Certificate of AnalysisSep 04, 2023 T112368
I2312672Certificate of AnalysisSep 04, 2023 T112368
I2312673Certificate of AnalysisSep 04, 2023 T112368
I2312677Certificate of AnalysisSep 04, 2023 T112368
I2312678Certificate of AnalysisSep 04, 2023 T112368
I2312681Certificate of AnalysisSep 04, 2023 T112368
I2312685Certificate of AnalysisSep 04, 2023 T112368
I2312686Certificate of AnalysisSep 04, 2023 T112368

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Propriedades químicas e físicas
SolubilidadeSlightly soluble in water; Soluble in Alcohol,Acetone,Ether
SensibilidadeLight sensitive.
Ponto de inflamação (°F)255℃
Ponto de inflamação (°C)255℃
Ponto de ebulição (°C)174°C
Ponto de fusão (°C)57-60°C
Peso molecular161.200 g/mol
XLogP31.800
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count1
Rotatable Bond Count2
Exact Mass161.084 Da
Monoisotopic Mass161.084 Da
Topological Polar Surface Area36.000 Ų
Heavy Atom Count12
Formal Charge0
Complexity149.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
FAQs e artigos
Citations of This Product
Referências
1. Zhang Junzhi, Lin Binyan, Zhang Ying, Hu Xiaochao, Liu Tongtong, Liu E-Hu, Liu Shijia.  (2024)  Baitouweng decoction alleviates ulcerative colitis by regulating tryptophan metabolism through DOPA decarboxylase promotion.  Frontiers in Pharmacology,      [PMID:38974042] [10.3389/fphar.2024.1423307]
2. Mengshi Xiao, Jiayuan Bi, Xinmiao Ren, Xiaodan Fu, Dongyu Li, Rong Li, Haijin Mou.  (2024)  Evaluation of potential prebiotic activity of a novel fucose-containing trisaccharide prepared from bacterial exopolysaccharides.  Food Bioscience,      [PMID:] [10.1016/j.fbio.2024.104380]
Calculadoras de soluções
Revisões

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