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 Formula: C₁₁H₂₄S Molecular Weight: 188.37 Beilstein Registry Number: 1(4)1838 EC Number: 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

Overview

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

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

Specifications & Purity

≥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

Storage

Room temperature,Argon charged

Shipped In

Normal

Purity

≥96%(GC)

Names and Identifiers

Pubchem Sid

504753854

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/504753854

Canonical Smiles

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

Isomeric SMILES

CCCCCCCCCCCS

PubChem CID

62570

UN Number

1228

Packing Group

II

Molecular Weight

188.37

Beilstein

1(4)1838

Reaxy-Rn

1736161

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Organosulfur compounds
• Class: 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

Chemical and Physical Properties

• Solubility: Insoluble in water
• Sensitivity: Air sensitive
• Refractive Index: 1.46
• Flash Point(°F): 219.9 °F
• Flash Point(°C): 109°C(lit.)
• Boil Point(°C): 104°C/3mmHg(lit.)
• Melt Point(°C): -3°C(lit.)
• Molecular Weight: 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