Determine the necessary mass, volume, or concentration for preparing a solution.
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
≥99%(GC) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at 2-8°C,Argon charged Ships Wet ice,FedEx DG Service 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 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Benzyl thiocyanate undergoes regioselective bond dissociation during its electrochemical reduction in acetonitrile at an inert electrode. It is added to stimulate the chlortetracycline biosynthesis during industrial fermentations. It undergoes biotransformation into dibenzyl disulphide by Streptomyces aureofaciens.
Benzyl thiocyanate was used to study the effects of various dietary compounds on the α-hydroxylation of N-nitrosopyrrolidine in male F344 rats in vitro
| Sonrisas canónicas | C1=CC=C(C=C1)CSC#N |
|---|---|
| IUPAC Name | benzyl thiocyanate |
| InChIKey | ABNDFSOIUFLJAH-UHFFFAOYSA-N |
| INCHI | 1S/C8H7NS/c9-7-10-6-8-4-2-1-3-5-8/h1-5H,6H2 |
| Isómeros SMILES | C1=CC=C(C=C1)CSC#N |
| WGK Alemania | 3 |
| RTECS | XK8155000 |
| Número ONU | 1759 |
| Grupo de embalaje | II |
| Peso molecular | 149.21 |
| Reaxy-Rn | 1859726 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1859726&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 | Benzenoids |
| Clase | Benzene and substituted derivatives |
| Subclass | Benzyl thiocyanates |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Benzyl thiocyanates |
| Alternative Parents | Thiocyanates Sulfenyl compounds Organopnictogen compounds Organonitrogen compounds Hydrocarbon derivatives |
| Molecular Framework | Aromatic homomonocyclic compounds |
| Substituents | Benzyl thiocyanate - Sulfenyl compound - Thiocyanate - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organosulfur compound - Organonitrogen compound - Aromatic homomonocyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as benzyl thiocyanates. These are aromatic compounds containing an thiocyanate group that is S-substituted to a benzyl group. |
| External Descriptors | a small molecule |
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Fecha | Articulo |
|---|---|---|---|
| Certificate of Analysis | Jun 09, 2026 | B152183 | |
| Certificate of Analysis | May 08, 2026 | B152183 | |
| Certificate of Analysis | May 08, 2026 | B152183 | |
| Certificate of Analysis | May 08, 2026 | B152183 | |
| Certificate of Analysis | Aug 12, 2025 | B152183 | |
| Certificate of Analysis | Aug 12, 2025 | B152183 | |
| Certificate of Analysis | May 26, 2022 | B152183 | |
| Certificate of Analysis | Oct 22, 2021 | B152183 |
| Solubilidad | solubility diethyl ether: soluble 0.5 g/10 mL, clear to very faintly turbid, colorless to almost colorless |
|---|---|
| Sensibilidad | Moisture sensitive |
| Punto de inflamación (°F) | 230 °F |
| Punto de inflamación (°C) | 110°C |
| Punto de ebullición (°C) | 256°C |
| Punto de fusión (°C) | 40-43℃ |
| Peso molecular | 149.210 g/mol |
| XLogP3 | 2.000 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 2 |
| Exact Mass | 149.03 Da |
| Monoisotopic Mass | 149.03 Da |
| Topological Polar Surface Area | 49.100 Ų |
| Heavy Atom Count | 10 |
| Formal Charge | 0 |
| Complexity | 129.000 |
| 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 |
| 1. Xiaopei Li, Xianxu Chu, Kefan Ying, Xi Chen, Peng Sun, Haiyun Xu, Lu Li, Jie Zhang, Wenjuan Li. (2025) Synthesis of Novel Organic Ni (II) N-isonicotinoylhydrazine-Carbothioamide Complexes and their Application in the Oxygen Evolution Reactions. Inorganic Chemistry Frontiers, [PMID:] [10.1039/D5QI00033E] |