≥90% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature,Argon charged Ships Normal Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 4 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Sodium thiophenolate can be prepared from the reaction of sodium and thiophenol in diethyl ether.
Sodium thiophenolate has been used for the synthesis of MCoTI-I and MCoTI-II cyclotides, which are naturally-occurring cyclic cystine-knot microprotein trypsin inhibitors. It may be employed in the following studies:
· As probe for the immunoassay and for the detection of label-free protein by surface-enhanced Raman scattering (SERS).
· Preparation of new cyclometalated 6-phenyl-4-(p-R-phenyl)-2,2′-bipyridyl (C--N--N)Pt(II) thiophenolate complexes.
· Synthesis of 1,3,5,7,9-pentakis(4-methoxyphenylthio)corannulene, 1,3,5,7,9-pentakis(2-naphthylthio)corannulene and 1,3,6,8-tetrakis(4-methoxyphenylthio)corannulene.
· Synthesis of Et4N+ salts of homoleptic arylthiolate Ti(IV) complex, [Ti(SPh)6]2-.
| Sonrisas canónicas | C1=CC=C(C=C1)[S-].[Na+] |
|---|---|
| IUPAC Name | sodium;benzenethiolate |
| InChIKey | RZWQDAUIUBVCDD-UHFFFAOYSA-M |
| INCHI | 1S/C6H6S.Na/c7-6-4-2-1-3-5-6;/h1-5,7H;/q;+1/p-1 |
| Isómeros SMILES | C1=CC=C(C=C1)[S-].[Na+] |
| WGK Alemania | 3 |
| PubChem CID | 4110039 |
| Peso molecular | 132.16 |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Benzenoids |
| Clase | Benzene and substituted derivatives |
| Subclass | Not available |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Benzene and substituted derivatives |
| Alternative Parents | Organosulfur compounds Organic sodium salts Hydrocarbon derivatives |
| Molecular Framework | Aromatic homomonocyclic compounds |
| Substituents | Monocyclic benzene moiety - Organic alkali metal salt - Hydrocarbon derivative - Organic sodium salt - Organic salt - Organosulfur compound - Aromatic homomonocyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as benzene and substituted derivatives. These are aromatic compounds containing one monocyclic ring system consisting of benzene. |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Fecha | Articulo |
|---|---|---|---|
 B2626619 | Certificate of Analysis | Jan 24, 2026 | S195897 |
| B2626620 | Certificate of Analysis | Jan 24, 2026 | S195897 |
| B2626621 | Certificate of Analysis | Jan 24, 2026 | S195897 |
| B2626622 | Certificate of Analysis | Jan 24, 2026 | S195897 |
| D2620095 | Certificate of Analysis | Jan 24, 2026 | S195897 |
| A2211582 | Certificate of Analysis | Feb 17, 2025 | S195897 |
| L2427369 | Certificate of Analysis | Dec 11, 2024 | S195897 |
| L2427371 | Certificate of Analysis | Dec 11, 2024 | S195897 |
| L2427373 | Certificate of Analysis | Dec 11, 2024 | S195897 |
| L2427375 | Certificate of Analysis | Dec 11, 2024 | S195897 |
| A2211581 | Certificate of Analysis | Oct 11, 2024 | S195897 |
| A2211609 | Certificate of Analysis | Oct 11, 2024 | S195897 |
| L2402586 | Certificate of Analysis | Jul 08, 2024 | S195897 |
| A2422192 | Certificate of Analysis | Dec 07, 2021 | S195897 |
| E2408023 | Certificate of Analysis | Dec 07, 2021 | S195897 |
| Sensibilidad | Air and moisture sensitive |
|---|---|
| Punto de fusión (°C) | >300 °C |
| Peso molecular | 132.160 g/mol |
| XLogP3 | |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 0 |
| Exact Mass | 132.001 Da |
| Monoisotopic Mass | 132.001 Da |
| Topological Polar Surface Area | 1.000 Ų |
| Heavy Atom Count | 8 |
| Formal Charge | 0 |
| Complexity | 50.500 |
| 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 | 2 |
| 1. Yumiao Dong, Qinhui Xie, Shuo Wu, Junbo Li, Lei Sun, Wei Ji. (2023) Revealing Adsorption Mechanism of p-Mercaptobenzoic Acid with TiO2 Surfaces Using Electric Field-Enhanced Semiconductor SERS. Journal of Physical Chemistry C, [PMID:] [10.1021/acs.jpcc.3c02113] |
| 2. Zhuoyao Li, Chengyu Zhang, Huixiang Sheng, Jin Wang, Yameng Zhu, Liuyingzi Yu, Junjie Wang, Qiming Peng, Gang Lu. (2022) Molecular Cocatalyst of p-Mercaptophenylboronic Acid Boosts the Plasmon-Mediated Reduction of p-Nitrothiophenol. ACS Applied Materials & Interfaces, [PMID:35943401] [10.1021/acsami.2c08327] |
| 3. Qilong Li, Na Li, Xiangqiang Pan, Jian Zhu. (2021) Photo masking via breaking alkyl CSe bond of selenium-containing maleimide polymers by ultraviolet light. EUROPEAN POLYMER JOURNAL, [PMID:] [10.1016/j.eurpolymj.2021.110764] |
| 4. Yu Ji, Qiang Yao, Weihong Cao, Yueying Zhao. (2021) A Probable Origin of Dibenzothiophenes in Coals and Oils. Energies, 14 (1): (234). [PMID:] [10.3390/en14010234] |
