2-Ethylhexyl Thioglycolate - ≥98%(GC) , CAS No.7659-86-1

CAS: 7659-86-1 Cat. No.: E156186 Formula: C₁₀H₂₀O₂S Peso molecolare: 204.33 Beilstein Registry Number: 9047470 Numero EC: 231-626-4

GRADE & PURITY ≥98%(GC)

Synonyms

Mercaptoacetic acid 2-ethylhexyl ester | NCGC00257281-01 | Thioglykolsaeure-2-aethylhexyl ester | 2-ethylhexyl 2-sulfanylethanoate | AKOS000120360 | LS-13895 | OWHSTLLOZWTNTQ-UHFFFAOYSA- | 2-Ethylhexyl thioglycolate, >=95.0% (GC) | Acetic acid, 2-mercapto

Storage

Room temperature

Shipped In

Normal

Specifications

Sinonimi

Mercaptoacetic acid 2-ethylhexyl ester | NCGC00257281-01 | Thioglykolsaeure-2-aethylhexyl ester | 2-ethylhexyl 2-sulfanylethanoate | AKOS000120360 | LS-13895 | OWHSTLLOZWTNTQ-UHFFFAOYSA- | 2-Ethylhexyl thioglycolate, >=95.0% (GC) | Acetic acid, 2-mercapto

Specifiche e purezza

≥98%(GC)

Condizioni di conservazione di stoccaggio

Room temperature

Spedito in

Normal

Purezza

≥98%(GC)

Nomi e identificatori

• Pubchem Sid: 504753183
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504753183
• Sorrisi canonici: CCCCC(CC)COC(=O)CS
• IUPAC Name: 2-ethylhexyl 2-sulfanylacetate
• InChIKey: OWHSTLLOZWTNTQ-UHFFFAOYSA-N
• INCHI: 1S/C10H20O2S/c1-3-5-6-9(4-2)7-12-10(11)8-13/h9,13H,3-8H2,1-2H3
• Isomeri SMILES: CCCCC(CC)COC(=O)CS
• WGK Germania: 3
• RTECS: AI7255000
• Peso molecolare: 204.33
• Beilstein: 9047470
• Reaxy-Rn: 9047474
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=9047474&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Classe Carboxylic acids and derivatives
      • Subclass Carboxylic acid derivatives

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Classe: Carboxylic acids and derivatives
• Subclass: Carboxylic acid derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: Carboxylic acid esters
• Alternative Parents: Monocarboxylic acids and derivatives Alkylthiols Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Carboxylic acid ester - Monocarboxylic acid or derivatives - 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 carboxylic acid esters. These are carboxylic acid derivatives in which the carbon atom from the carbonyl group is attached to an alkyl or an aryl moiety through an oxygen atom (forming an ester group).
• 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

Meccanismi d'azione

Proprietà chimiche e fisiche

• Solubilità: Solubility in water: Practically Insoluble; Degree of Solubility in water: 0.03 g/l 23 °C
• Indice di rifrazione: 1.46
• Rotazione specifica [α]: 1.461
• Punto di infiammabilità (°F): 132.8 °F
• Punto di infiammabilità (°C): 136°C
• Punto di ebollizione (°C): 255-260°C
• Peso molecolare: 204.330 g/mol
• XLogP3: 3.600
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 8
• Exact Mass: 204.118 Da
• Monoisotopic Mass: 204.118 Da
• Topological Polar Surface Area: 27.300 Ų
• Heavy Atom Count: 13
• Formal Charge: 0
• Complexity: 137.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 1
• 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. Jie Mao, Jing Li, Wang Lin, Faliang Luo.  (2023)  Polybutadiene Dielectric Elastomers with High Dielectric Constant and Ultralow Dielectric Loss via Tuning Grafted Polar Groups.  MACROMOLECULAR RAPID COMMUNICATIONS,  44  (10): (2200971).  [PMID:37002911] [10.1002/marc.202200971]

2. Xing Liu, Zhenzhi Liu, Houqun Xiao, Lijing Han, Jianqing Zhao.  (2025)  Phosphorus-Containing Polyimidothioether as a Latent Curing Agent and Flame Retardant for One-Component Epoxy Resins.  ACS Applied Polymer Materials,      [PMID:] [10.1021/acsapm.5c02469]

3. Zhengyong Song, Qian Zhang, Shuming Wen.  (2026)  Synergistic chemical bonding and hydrogen bonding interactions enable efficient collection for non-activated ZnSO4-depressed sphalerite by 2-ethylhexyl thioglycolate.  SEPARATION AND PURIFICATION TECHNOLOGY,      [PMID:] [10.1016/j.seppur.2026.139446]