Interesting facts
Interesting Facts about 1-Isothiocyanatobutane
1-Isothiocyanatobutane is a fascinating compound that falls within the category of isothiocyanates, known for their intriguing chemical properties and biological effects. Here are some notable aspects:
- Natural Sources: Isothiocyanates are commonly found in cruciferous vegetables such as broccoli, Brussels sprouts, and mustard greens. 1-Isothiocyanatobutane can be derived from the breakdown of glucosinolates in these plants, which contributes to their distinctive flavors and health benefits.
- Biological Activity: This compound has attracted the interest of researchers due to its potential anti-cancer properties. Studies suggest that isothiocyanates may help in the detoxification processes and apoptosis (programmed cell death) in cancerous cells.
- Flavor and Aroma: 1-Isothiocyanatobutane contributes to the characteristic pungency of mustard and horseradish. Its presence in various culinary dishes adds an exciting flavor profile that is both spicy and aromatic.
- Industrial Applications: Beyond its culinary use, this compound is explored for its utility in agriculture as a bio-pesticide and bio-fumigant due to its natural insect-repellent properties.
- Chemical Reactivity: The isothiocyanate functional group is highly reactive, allowing 1-isothiocyanatobutane to participate in various nucleophilic reactions, which can be of interest in synthetic organic chemistry.
- Environmental Impact: As a natural compound, isothiocyanates are considered greener alternatives in pest management, highlighting the importance of studying such compounds for sustainable agricultural practices.
In summary, 1-isothiocyanatobutane is a multifaceted compound that plays a crucial role in both biology and industry. Its unique properties make it a lively subject of study for chemists and biologists alike. As the saying goes, "What grows together, goes together," and this compound exemplifies the deep connection between nature and chemistry!
Synonyms
Butyl isothiocyanate
1-Isothiocyanatobutane
Butane, 1-isothiocyanato-
1-isothiocyanato-butane
NSC 194808
EINECS 209-770-4
UNII-4Y31800S6C
CHEBI:50534
AI3-18424
n-Butyl isothio cyanate
Butyl isothiocyanate, 8CI
4Y31800S6C
NSC-194808
DTXSID7060467
FEMA NO. 4082
BUTYL ISOTHIOCYANATE [FHFI]
BUTYL ISOTHIOCYANATE [USP-RS]
BUTYL ISOTHIOCYANATE (USP-RS)
Butyl isothiocyanic acid
N-Butyl isothiocyanic acid
Isothiocyanate, butyl ester
Isothiocyanate N-butyl ester
DTXCID6042575
209-770-4
limqqadueulbso-uhfffaoysa-n
592-82-5
n-Butyl isothiocyanate
Butylisothiocyanate
1-butyl isothiocyanate
ISOTHIOCYANIC ACID, BUTYL ESTER
Isothiocyanic acid n-butyl ester
MFCD00004824
Butylsenfoel
BuNCS
n-butylisothiocyanate
n-butyl-isothiocyanate
1-Isothiocyanatobutane #
Butyl isothiocyanate, 99%
SCHEMBL152568
Isothiocyanic Acid Butyl Ester
CHEMBL1814588
NSC194808
AKOS000118861
Butyl isothiocyanate, analytical standard
DB-022994
I0249
NS00022461
EN300-19446
D91107
A832240
Q27122105
F1915-0013
Z104473876
Butyl isothiocyanate, United States Pharmacopeia (USP) Reference Standard
Solubility of 1-Isothiocyanatobutane
1-Isothiocyanatobutane, with the chemical formula C4H7NCS, showcases interesting solubility characteristics that depend on various factors, including temperature and the presence of different solvents.
Key Solubility Traits:
In conclusion, while 1-isothiocyanatobutane demonstrates some solubility in polar organic solvents, its hydroxyl affinity diminishes significantly in water, making it a compound that primarily thrives in less polar environments. Recognizing these solubility aspects is crucial for applications involving this compound, as it influences its reactivity and usability in various chemical processes.