1-Undecanethiol - ≥96%(GC), used for UDT can be used to functionalize polycarbonate filter membrane for immunological experiments which can further be used in the fabrication of plasmonic flow through biosensor based applications. SAM of UDT can be used i

CAS: 5332-52-5 Cat. No.: U162892 Formule: C₁₁H₂₄S Poids moléculaire: 188.37 Beilstein Registry Number: 1(4)1838 Numéro CE: 628-713-8 PubChem CID: 62570

GRADE & PURITY ≥96%(GC)

Synonyms

DTXSID4074564 | AKOS015903186 | YY1144Q77A | 1-UDT | NSC4031 | NSC-4031 | UNII-YY1144Q77A | 1-mercaptoundecane | undecane-1-thiol | SCHEMBL131363 | undecylmercaptan | NSC 4031 | BP-27935 | MFCD00022097 | Undecyl mercaptan

Storage

Room temperature,Argon charged

Shipped In

Normal

Application

Drug Delivery, Surface Modification, PEGylation of Protein, Peptide & Oligo

Vue d’ensemble

1-Undecanethiol (UDT) is an alkanethiol that forms a self-assembled monolayer (SAM) on a variety of surfaces. It immobilizes the surface atoms and enhances the absorption of proteins. It can be synthesized by reacting bromo-1-undecanol and thiourea and subsequent purification using ethyl acetate.

Specifications

Synonymes

DTXSID4074564 | AKOS015903186 | YY1144Q77A | 1-UDT | NSC4031 | NSC-4031 | UNII-YY1144Q77A | 1-mercaptoundecane | undecane-1-thiol | SCHEMBL131363 | undecylmercaptan | NSC 4031 | BP-27935 | MFCD00022097 | Undecyl mercaptan

Spécifications et pureté

≥96%(GC)

Application

UDT can be used to functionalize polycarbonate filter membrane for immunological experiments which can further be used in the fabrication of plasmonic flow through biosensor based applications. SAM of UDT can be used in the colloidal gold enhanced immunoa

Conditions de stockage de stockage

Room temperature,Argon charged

Expédié en

Normal

Pureté

≥96%(GC)

Noms et identifiants

• Pubchem Sid: 504753854
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504753854
• Sourires canoniques: CCCCCCCCCCCS
• IUPAC Name: undecane-1-thiol
• InChIKey: CCIDWXHLGNEQSL-UHFFFAOYSA-N
• INCHI: 1S/C11H24S/c1-2-3-4-5-6-7-8-9-10-11-12/h12H,2-11H2,1H3
• Isomères SMILES: CCCCCCCCCCCS
• PubChem CID: 62570
• Numéro ONU: 1228
• Groupe d'emballage: II
• Poids moléculaire: 188.37
• Beilstein: 1(4)1838
• Reaxy-Rn: 1736161

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organosulfur compounds
    • Classe Thiols
      • Subclass Alkylthiols

• Kingdom: Organic compounds
• Superclass: Organosulfur compounds
• Classe: Thiols
• Subclass: Alkylthiols
• Intermediate Tree Nodes: Not available
• Direct Parent: Alkylthiols
• Alternative Parents: Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Alkylthiol - Hydrocarbon derivative - Aliphatic acyclic compound
• Description: This compound belongs to the class of organic compounds known as alkylthiols. These are organic compounds containing the thiol functional group linked to an alkyl chain.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Propriétés chimiques et physiques

• Solubilité: Insoluble in water
• Sensibilité: Air sensitive
• Indice de réfraction: 1.46
• Point d'éclair (°F): 219.9 °F
• Point d'éclair (°C): 109°C(lit.)
• Point d'ébullition (°C): 104°C/3mmHg(lit.)
• Point de fusion (°C): -3°C(lit.)
• Poids moléculaire: 188.380 g/mol
• XLogP3: 5.600
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 9
• Exact Mass: 188.16 Da
• Monoisotopic Mass: 188.16 Da
• Topological Polar Surface Area: 1.000 Ų
• Heavy Atom Count: 12
• Formal Charge: 0
• Complexity: 71.400
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• 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

Références

1. Ximing Huang, Jingchao Chen, Chunxia Yan, Haixia Guo, Huibo Shao.  (2020)  Probing Charge Reversal of Zwitterion at Defects on Self-Assembled Monolayers by Scanning Electrochemical Microscopy.  Journal of Physical Chemistry C,      [PMID:] [10.1021/acs.jpcc.0c01661]

2. Yan Zhang, Jianlin Yang, Yali Zhao, Zhecun Wang.  (2025)  Molecularly engineered under-liquid dual superlyophobic coatings for efficient and on-demand oil/water separation.  JOURNAL OF MEMBRANE SCIENCE,      [PMID:] [10.1016/j.memsci.2025.124603]