16-mercaptohexadecanoic acid - ≥95% , CAS No.69839-68-5

CAS: 69839-68-5 Cat. No.: M304433 Formula: C₁₆H₃₂O₂S Peso molecolare: 288.49 Numero EC: 628-111-5

GRADE & PURITY ≥95%

Synonyms

MHDA | C16H32O2S | INOAASCWQMFJQA-UHFFFAOYSA-N | AMY37962 | 16-Mercaptohexadecanoic acid, 99% | DTXSID00393287 | Hexadecanoic acid, 16-mercapto- | 16-Mercaptohexadecanoic acid, 90% | SCHEMBL49347 | 16-Mercaptohexadecanoic acid | D70988 | MFCD00674018 | BS

Storage

Store at 2-8°C,Argon charged

Shipped In

Wet ice

Panoramica

product description：

16-Mercaptohexadecanoic acid (MHA) is an alkanethiol with long chained −CH2 groups, which form a self-assembled monolayer (SAM) on a wide range of substrates.

application：

MHA forms a SAM on gold surfaces by pen lithography (PPL). It finds potential application in bio-engineering. It can also be used to functionalize gold-dypiramids, which can fabricate nano-resonators for shell-isolated nanoparticle enhanced Raman-spectroscopy (SHINERS).

Formation of interchain carboxylic anhydrides on self-assembled monolayers with Fluoro N,N,N′,N′-tetramethylforamidinium hexafluorophosphate. This compound is used in self-assembly to produce hydrophilic SAMs. The resulting monolayers which are terminated with carboxylic acids can be further functionalized with various amines and alcohols to introduce more complex end groups or multiple layers.

Specifications

Sinonimi

MHDA | C16H32O2S | INOAASCWQMFJQA-UHFFFAOYSA-N | AMY37962 | 16-Mercaptohexadecanoic acid, 99% | DTXSID00393287 | Hexadecanoic acid, 16-mercapto- | 16-Mercaptohexadecanoic acid, 90% | SCHEMBL49347 | 16-Mercaptohexadecanoic acid | D70988 | MFCD00674018 | BS

Specifiche e purezza

≥95%

Condizioni di conservazione di stoccaggio

Store at 2-8°C,Argon charged

Spedito in

Wet ice

Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.

Purezza

≥95%

Nomi e identificatori

• Pubchem Sid: 504762596
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504762596
• Sorrisi canonici: C(CCCCCCCC(=O)O)CCCCCCCS
• IUPAC Name: 16-sulfanylhexadecanoic acid
• InChIKey: INOAASCWQMFJQA-UHFFFAOYSA-N
• INCHI: 1S/C16H32O2S/c17-16(18)14-12-10-8-6-4-2-1-3-5-7-9-11-13-15-19/h19H,1-15H2,(H,17,18)
• Isomeri SMILES: C(CCCCCCCC(=O)O)CCCCCCCS
• WGK Germania: 3
• Peso molecolare: 288.49
• Reaxy-Rn: 2257927
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2257927&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Lipids and lipid-like molecules
    • Classe Fatty Acyls
      • Subclass Fatty acids and conjugates

• Kingdom: Organic compounds
• Superclass: Lipids and lipid-like molecules
• Classe: Fatty Acyls
• Subclass: Fatty acids and conjugates
• Intermediate Tree Nodes: Not available
• Direct Parent: Long-chain fatty acids
• Alternative Parents: Thia fatty acids Straight chain fatty acids Monocarboxylic acids and derivatives Carboxylic acids Alkylthiols Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Long-chain fatty acid - Thia fatty acid - Straight chain fatty acid - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Alkylthiol - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organosulfur compound - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as long-chain fatty acids. These are fatty acids with an aliphatic tail that contains between 13 and 21 carbon atoms.
• 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

Proprietà chimiche e fisiche

• Sensibilità: air sensitive
• Punto di infiammabilità (°C): 208.8℃
• Punto di ebollizione (°C): 421.7℃at 760 mmHg
• Punto di fusione (°C): 65-69 °C
• Peso molecolare: 288.500 g/mol
• XLogP3: 5.700
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 15
• Exact Mass: 288.212 Da
• Monoisotopic Mass: 288.212 Da
• Topological Polar Surface Area: 38.300 Ų
• Heavy Atom Count: 19
• Formal Charge: 0
• Complexity: 195.000
• 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

Riferimenti

1. Jiaojiao Fang, Chengyang Zhu, Yaru Ni, Chunhua Lu, Zhongzi Xu.  (2023)  Double local electromagnetic fields collaboratively enhanced triplet–triplet annihilation upconversion for efficient photocatalysis.  Catalysis Science & Technology,  13  (7): (2151-2159).  [PMID:] [10.1039/D2CY01649D]

2. Jian Wang, Essalhi Fatima-Ezzahra, Jie Dai, Yanlei Liu, Chengjie Pei, Hai Li, Zhiwei Wang, Xiao Huang.  (2022)  Ligand-assisted deposition of ultra-small Au nanodots on Fe2O3/reduced graphene oxide for flexible gas sensors.  Nanoscale Advances,  4  (5): (1345-1350).  [PMID:36133674] [10.1039/D1NA00734C]

3. Huiying Guo, Wanwan Cao, Guodong Yang, Ruoxu Wang, Hongyu Chen.  (2025)  In-ex site selectivity: a novel mechanism for the controlled fabrication of hollow multi-shelled nanostructures.  JOURNAL OF COLLOID AND INTERFACE SCIENCE,      [PMID:40876332] [10.1016/j.jcis.2025.138805]