Tryptophol - 10mM in DMSO , CAS No.526-55-6

CAS: 526-55-6 Cat. No.: T424520 Formule: C10H11NO Poids moléculaire: 161.2 Beilstein Registry Number: 125553 Numéro CE: 208-393-2 PubChem CID: 10685
DISPONIBLE À COMMANDE
GRADE & PURITY 10mM in DMSO
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
Store at -80°C
Shipped In
Dry ice packs + Cold packs
★
Size
Allemagne (EU)
USA*
Price
Qty
1ml
T424520-1ml
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1 En stock
38,96€
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Why this grade

10mM in DMSO for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at -80°C Ships Dry ice packs + Cold packs 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.

Vue d’ensemble

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

Synonymes
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
Spécifications et pureté
10mM in DMSO
Conditions de stockage de stockage
Store at -80°C
Expédié en
Dry ice packs + Cold packs
Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.
Noms et identifiants
Pubchem Sid528775082
Sourires canoniquesC1=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
Isomères SMILES C1=CC=C2C(=C1)C(=CN2)CCO
WGK Allemagne 3
RTECS KL3685000
PubChem CID 10685
Poids moléculaire 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
DescriptionThis 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
Structure 3D
Modèle de structure chimique interactif





Cibles associées (humaines)
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
Cibles associées (non humaines)
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
Mécanismes d'action
Certificats (CoA, COO, BSE/TSE et tableau d'analyse)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Propriétés chimiques et physiques
SensibilitéLight sensitive.
Point d'éclair (°F)255℃
Point d'éclair (°C)255℃
Point d'ébullition (°C)174°C
Point de fusion (°C)57-60°C
Poids moléculaire161.200 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
FAQ et articles
Citations of This Product
Références
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]
Calculateurs de solution
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