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Isopropyl isothiocyanate is an isothiocyanate derivative. It has been identified as one of the volatile components in the following:
Molecular conformations of isopropyl isothiocyanate in gas phase have been determined by electron diffraction studies. It has been synthesized by employing isopropyl amine as a starting reagent.
- seed kernel and leaf of Moringa peregrina (Forssk.) Fiori, Agricolt1
- essential oil isolated from Upland Wasabi
- hydrodistillates of hedge mustard (Sysimbrium officinale)
Molecular conformations of isopropyl isothiocyanate in gas phase have been determined by electron diffraction studies. It has been synthesized by employing isopropyl amine as a starting reagent.
애플리케이션
Isopropyl isothiocyanate may be used to synthesize 4-bromo-5,6-dichloro-2-isopropylaminobenzimidazole.
신호어
Warning
유해 및 위험 성명서
Hazard Classifications
Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3
표적 기관
Respiratory system
Storage Class Code
3 - Flammable liquids
WGK
WGK 3
Flash Point (°F)
104.0 °F - closed cup
Flash Point (°C)
40 °C - closed cup
개인 보호 장비
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
이미 열람한 고객
Analysis of volatile components in essential oil of upland wasabi and their inhibitory effects on platelet aggregation.
Bioscience, Biotechnology, and Biochemistry, 58(12), 2131-2135 (1994)
Chemistry & biodiversity, 7(8), 2023-2034 (2010-08-24)
Volatile compounds of hedge mustard (Sysimbrium officinale) have been investigated for the first time. Forthy-two compounds were identified after hydrodistillation (without or upon autolysis) after gas chromatography and gas chromatography/mass spectrometry analyses. In addition, after decoction and hydrolysis of O-glycosides
Electron diffraction investigation of the molecular structures of isopropyl isocyanate and isopropyl isothiocyanate.
Journal of Molecular Structure, 140(3), 199-207 (1986)
A general and facile one-pot process of isothiocyanates from amines under aqueous conditions.
Beilstein Journal of Organic Chemistry, 8(1), 61-70 (2012)
Synthesis and antiviral evaluation of halogenated ?-d-and-l-erythrofuranosylbenzimidazoles.
Journal of Medicinal Chemistry, 43(12), 2464-2472 (2000)
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