1-Naphthyl isothiocyanate
98%
- Product Code: 114957
Alias:
1-naphthyl isothiocyanate; 1-naphthyl isothiocyanate, α-naphthyl isothiocyanate, α-naphthyl isothiocyanate
CAS:
551-06-4
| Molecular Weight: | 185.24 g./mol | Molecular Formula: | C₁₁H₇NS |
|---|---|---|---|
| EC Number: | 208-990-8 | MDL Number: | MFCD00003882 |
| Melting Point: | 55.5-57 °C(lit.) | Boiling Point: | |
| Density: | Storage Condition: | 2~8°C, dry |
Product Description:
1-Naphthyl isothiocyanate is primarily used in biochemical research as a reagent for the detection and quantification of amino acids, peptides, and proteins. It reacts with primary amines to form stable derivatives, making it valuable in chromatographic analysis and mass spectrometry for identifying and studying these compounds. Additionally, it is employed in the synthesis of organic compounds, particularly in the preparation of heterocyclic structures, due to its ability to introduce the isothiocyanate functional group. In toxicology studies, it serves as a tool to investigate the effects of isothiocyanates on biological systems, providing insights into their mechanisms of action and potential health impacts.
Product Specification:
| Test | Specification |
|---|---|
| Melting Point | 53-57 |
| Purity (GC) | 98-100 |
| Appearance | White To Off-White To Yellow Powder Or Crystals |
| Infrared Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | €26.38 |
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| 5.000 | 10-20 days | €103.68 |
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| 10.000 | 10-20 days | €168.05 |
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| 25.000 | 10-20 days | €361.43 |
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| 100.000 | 10-20 days | €1,339.15 |
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1-Naphthyl isothiocyanate
1-Naphthyl isothiocyanate is primarily used in biochemical research as a reagent for the detection and quantification of amino acids, peptides, and proteins. It reacts with primary amines to form stable derivatives, making it valuable in chromatographic analysis and mass spectrometry for identifying and studying these compounds. Additionally, it is employed in the synthesis of organic compounds, particularly in the preparation of heterocyclic structures, due to its ability to introduce the isothiocyanate functional group. In toxicology studies, it serves as a tool to investigate the effects of isothiocyanates on biological systems, providing insights into their mechanisms of action and potential health impacts.
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