≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature 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 2 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Product description：
Butyl sulfide is a volatile sulfur compound that can be used as a flavoring agent.
Application：
Di-n-butyl sulfide is generally used as an agricultural intermediate, a sulfiding agent, a refinery catalyst, a lubricant additive, a gas odorant and a processing aid in mining applications. It finds application as an internal standard in X-ray fluorescence spectrometry (XRF) measurements of sulfur in oils and other liquid hydrocarbon matrices.
| Pubchem Sid | 528769558 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/528769558 |
| Sorrisi canonici | CCCCSCCCC |
| IUPAC Name | 1-butylsulfanylbutane |
| InChIKey | HTIRHQRTDBPHNZ-UHFFFAOYSA-N |
| INCHI | 1S/C8H18S/c1-3-5-7-9-8-6-4-2/h3-8H2,1-2H3 |
| Isomeri SMILES | CCCCSCCCC |
| WGK Germania | 2 |
| RTECS | ER6417000 |
| Peso molecolare | 146.29 |
| Beilstein | 1370 |
| Reaxy-Rn | 1732829 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1732829&ln= |
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 | Organosulfur compounds |
| Classe | Thioethers |
| Subclass | Dialkylthioethers |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Dialkylthioethers |
| Alternative Parents | Sulfenyl compounds Hydrocarbon derivatives |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Dialkylthioether - Sulfenyl compound - Hydrocarbon derivative - Aliphatic acyclic compound |
| Descrizione | This compound belongs to the class of organic compounds known as dialkylthioethers. These are organosulfur compounds containing a thioether group that is substituted by two alkyl groups. |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Data | Oggetto |
|---|---|---|---|
 A2207800 | Certificate of Analysis | Jul 15, 2025 | B136661 |
| A2207801 | Certificate of Analysis | Jul 15, 2025 | B136661 |
| H2304285 | Certificate of Analysis | May 12, 2025 | B136661 |
| H2304300 | Certificate of Analysis | May 12, 2025 | B136661 |
| H2304317 | Certificate of Analysis | May 12, 2025 | B136661 |
| J2115501 | Certificate of Analysis | Apr 03, 2025 | B136661 |
| L2206546 | Certificate of Analysis | Sep 19, 2024 | B136661 |
| L2206547 | Certificate of Analysis | Sep 19, 2024 | B136661 |
| L2206551 | Certificate of Analysis | Sep 19, 2024 | B136661 |
| J2115498 | Certificate of Analysis | Jul 07, 2023 | B136661 |
| I1923048 | Certificate of Analysis | May 06, 2023 | B136661 |
| Solubilità | Silghtly miscible with water. Miscible with olive oil and almond oil |
|---|---|
| Indice di rifrazione | 1.452 |
| Punto di infiammabilità (°F) | 170.6 °F |
| Punto di infiammabilità (°C) | 76°C(lit.) |
| Punto di ebollizione (°C) | 188-189 °C |
| Punto di fusione (°C) | −76 °C |
| Peso molecolare | 146.300 g/mol |
| XLogP3 | 3.400 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 6 |
| Exact Mass | 146.113 Da |
| Monoisotopic Mass | 146.113 Da |
| Topological Polar Surface Area | 25.300 Ų |
| Heavy Atom Count | 9 |
| Formal Charge | 0 |
| Complexity | 37.800 |
| 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. Jiahao Song, Hao Wu, Kaihu Zhang, Ruirui Liu, Yunfan Yang, Xinyue Zhang, Ahmed Elsherif, Ning Ma, Alaa S. Abd-El-Aziz. (2025) Nanoarchitectonics with designed sulfur-based functionalized azobenzene ionic liquids for low-temperature UV light switching systems. JOURNAL OF MOLECULAR LIQUIDS, [PMID:] [10.1016/j.molliq.2025.126880] |
| 2. Lu Chunyan, Li Mingjin, Li Wen, Deng Haoyun, Jiang Jutao, Wang Pengxi, Yang Biao, Yang Cheng, Li Xiaodong, Hu Ziyang, Zhang Wenjun. (2026) Near-Surface Sulfidation-Induced p-n Junction Enabling High-Efficiency Inverted Perovskite Solar Cells. ACS Applied Materials & Interfaces, 18 (35): (48341-48350). [PMID:42678027] [10.1021/acsami.6c07884] |
