Determine the necessary mass, volume, or concentration for preparing a solution.
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| SKU | Size | Availability |
Price | Qty |
|---|---|---|---|---|
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B151928-100mg
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100mg |
3
|
$16.90
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B151928-250mg
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250mg |
3
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$31.90
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B151928-1g
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1g |
3
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$96.90
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B151928-5g
|
5g |
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
|
$372.90
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B151928-25g
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25g |
1
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$1,675.90
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| Synonyms | MFCD00142541 | 1,4-Benzenedithiol | BBL103921 | Dithiohydroquinone | SCHEMBL64710 | GEO-04155 | CALCIUMUNDECYLENATE | C6H6S2 | 4-mercaptothiophenol | B1505 | DTXSID80405615 | AMY22355 | 1,4-Benzenendithiol | AKOS005207204 | MS-20722 | FT-0606769 | benzene |
|---|---|
| Specifications & Purity | ≥98%(GC) |
| Storage Temp | Store at 2-8°C,Argon charged |
| Shipped In |
Wet ice This product requires cold chain shipping. Ground and other economy services are not available. |
| Product Description |
It is used in single molecule junctions in electronic devices and nanomaterial synthesis. Benzene-1,4-dithiol (BDT) is a class of aromatic dithiol that can be used to form a self-assembled monolayer (SAM) on a variety of surfaces. |
Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Benzenoids |
| Class | Thiophenols |
| Subclass | Not available |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Thiophenols |
| Alternative Parents | Benzene and substituted derivatives Thiols Hydrocarbon derivatives |
| Molecular Framework | Aromatic homomonocyclic compounds |
| Substituents | Thiophenol - Monocyclic benzene moiety - Arylthiol - Hydrocarbon derivative - Organosulfur compound - Aromatic homomonocyclic compound |
| Description | This compound belongs to the class of organic compounds known as thiophenols. These are compounds containing a thiophenol ring, which a phenol derivative obtained by replacing the oxygen atom from the hydroxyl group (attached to the benzene) by a sulfur atom. |
| External Descriptors | Not available |
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| IUPAC Name | benzene-1,4-dithiol |
|---|---|
| INCHI | InChI=1S/C6H6S2/c7-5-1-2-6(8)4-3-5/h1-4,7-8H |
| InChIKey | WYLQRHZSKIDFEP-UHFFFAOYSA-N |
| Smiles | C1=CC(=CC=C1S)S |
| Isomeric SMILES | C1=CC(=CC=C1S)S |
| Molecular Weight | 142.23 |
| Beilstein | 6(4)5840 |
| Reaxy-Rn | 1680022 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1680022&ln= |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Date | Item |
|---|---|---|---|
| Certificate of Analysis | Mar 28, 2023 | B151928 | |
| Certificate of Analysis | Mar 28, 2023 | B151928 | |
| Certificate of Analysis | Mar 28, 2023 | B151928 | |
| Certificate of Analysis | Mar 28, 2023 | B151928 | |
| Certificate of Analysis | Jun 06, 2022 | B151928 | |
| Certificate of Analysis | Jun 06, 2022 | B151928 | |
| Certificate of Analysis | Jun 06, 2022 | B151928 | |
| Certificate of Analysis | Jun 06, 2022 | B151928 | |
| Certificate of Analysis | Jun 06, 2022 | B151928 | |
| Certificate of Analysis | Jun 06, 2022 | B151928 | |
| Certificate of Analysis | Jun 06, 2022 | B151928 | |
| Certificate of Analysis | Jun 06, 2022 | B151928 | |
| Certificate of Analysis | Jun 06, 2022 | B151928 |
| Solubility | Soluble in water. |
|---|---|
| Sensitivity | Air & Moisture Sensitive |
| Melt Point(°C) | 96.0 - 99.0 °C |
| Molecular Weight | 142.200 g/mol |
| XLogP3 | 2.100 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 0 |
| Exact Mass | 141.991 Da |
| Monoisotopic Mass | 141.991 Da |
| Topological Polar Surface Area | 2.000 Ų |
| Heavy Atom Count | 8 |
| Formal Charge | 0 |
| Complexity | 54.900 |
| 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 |
| 1. Siyu Wei, Xinfang Wang, Xinyu Zhao, Ke Zhao, Linzhe Xu, Yingbo Chen. (2023) Detection of pesticide residues on flexible and transparent fluorinated polyimide film based on surface-enhanced Raman spectroscopy technology. ANALYTICA CHIMICA ACTA, 1283 (341958). |
| 2. Zhenzhen Feng, Xiaomeng She, Jian Peng, Yujie Qiang, Song Zhang. (2023) Robust corrosion protection of Ni-thiolate coordination polymer/Mg(OH)2 coating on magnesium alloy AZ31. Journal of Materials Research and Technology-JMR&T, 26 (2407). |
| 3. Guangyuan Hu, Zhiwei Wang, Weiye Zhang, Hongxing He, Yi Zhang, Xiujun Deng, Weili Li. (2023) MIL-161 Metal–Organic Framework for Efficient Au(III) Recovery from Secondary Resources: Performance, Mechanism, and DFT Calculations. MOLECULES, 28 (14): (5459). |
| 4. Qianqian Wang, Hao Cui, Xiaolin Wang, Ziyu Hu, Peipei Tao, Mingyang Li, Jianlong Wang, Yaping Tang, Hong Xu, Xiangming He. (2023) Exceptional Light Sensitivity by Thiol–Ene Click Lithography. Journal of the American Chemical Society, 145 (5): (3064–3074). |
| 5. Fu Wan, Yu Lei, Changding Wang, Xinyuan Zhang, Honglin He, Lei Jia, Tingting Wang, Weigen Chen. (2022) Highly sensitive and reproducible CNTs@Ag modified Flower-Like silver nanoparticles for SERS situ detection of transformer Oil-dissolved furfural. SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY, 273 (121067). |
| 6. Haoyu Cai, Guojun Weng, Jianjun Li, Gaofeng Wu, Jian Zhu, Junwu Zhao. (2025) BDT mediated asymmetric deposition of Ag on gold nanobipyramids for SERS detection of drug residues in aquaculture water. COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS, 713 (136558). |
| 7. Xinyuan Bi, Zhicheng He, Zhewen Luo, Wensi Huang, Xingxing Diao, Jian Ye. (2024) Digital colloid-enhanced Raman spectroscopy for the pharmacokinetic detection of bioorthogonal drugs. Chemical Science, |
| 8. Yizhan Wang, Yunhui Shi, Jiawei Qiu, JiaBao Cheng, Yao Xu, Yongxin Wang. (2025) Insights into molecular interactions at organic-MBene heterointerfaces for efficient Zn-ion storage. JOURNAL OF COLLOID AND INTERFACE SCIENCE, 678 (95). |
| 9. Jing Huang, Li Zou, Shuxiang Wang, Yijia Zhang, Pingping Yang, Wenyan Tao, Jiale Xie. (2024) In-situ electrochemical activation of a nickel metal-organic framework modified TiO2 photoanode for urea photoelectrocatalysis. JOURNAL OF SOLID STATE CHEMISTRY, 336 (124779). |
| 10. Qinglian Hu, Jingyu Li, Tong Wang, Xiangchi Xu, Yuxuan Duan, Yuanxiang Jin. (2024) Polyphenolic Nanoparticle-Modified Probiotics for Microenvironment Remodeling and Targeted Therapy of Inflammatory Bowel Disease. ACS Nano, 18 (20): (12917-12932). |
| 11. Linchun Nie, Jiazhi Xia, Jiawei Liao, Na Liu, Meiling Xu, Dejing Meng, Wenjing Liu, Qingxiang Zhou, Chunmao Chen. (2025) Rapid visual detection of glutathione in vegetables and distinguishing multiple sulfur-containing compounds by smartphone-assisted sensor based on calcined PPy@CuNi-ZIF-67 nanozyme with enhanced oxidase-like activity. FOOD CHEMISTRY, 474 (143189). |
| 12. Linchun Nie, Liushan Jiang, Shuangying Li, Denghao Song, Guangyu Dong, Lutong Bu, Chunmao Chen, Qingxiang Zhou. (2024) Smartphone-assisted array discrimination of sulfur-containing compounds and colorimetric−fluorescence dual-mode sensor for detection of 1,4-benzenedithiol based on peroxidase-like nanozyme g-C3N4@Cu, N-CDs. TALANTA, 275 (126119). |