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Merck
모든 사진(2)

Key Documents

476013

Sigma-Aldrich

Isopropyl isothiocyanate

97%

동의어(들):

Isopropyl mustard oil

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About This Item

Linear Formula:
(CH3)2CHNCS
CAS Number:
Molecular Weight:
101.17
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

분석

97%

refractive index

n20/D 1.493 (lit.)

bp

29-30 °C/10 mmHg (lit.)

density

0.948 g/mL at 25 °C (lit.)

SMILES string

CC(C)N=C=S

InChI

1S/C4H7NS/c1-4(2)5-3-6/h4H,1-2H3

InChI key

VHBFEIBMZHEWSX-UHFFFAOYSA-N

유사한 제품을 찾으십니까? 방문 제품 비교 안내

일반 설명

Isopropyl isothiocyanate is an isothiocyanate derivative. It has been identified as one of the volatile components in the following:
  • 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.

픽토그램

FlameExclamation mark

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


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시험 성적서(COA)

Lot/Batch Number

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이 제품을 이미 가지고 계십니까?

문서 라이브러리에서 최근에 구매한 제품에 대한 문서를 찾아보세요.

문서 라이브러리 방문

Analysis of volatile components in essential oil of upland wasabi and their inhibitory effects on platelet aggregation.
Kumagai H, et al.
Bioscience, Biotechnology, and Biochemistry, 58(12), 2131-2135 (1994)
Ivica Blazević et al.
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.
Cradock S, et al.
Journal of Molecular Structure, 140(3), 199-207 (1986)
A general and facile one-pot process of isothiocyanates from amines under aqueous conditions.
Sun N, et al.
Beilstein Journal of Organic Chemistry, 8(1), 61-70 (2012)
Synthesis and antiviral evaluation of halogenated ?-d-and-l-erythrofuranosylbenzimidazoles.
Gudmundsson KS, et al.
Journal of Medicinal Chemistry, 43(12), 2464-2472 (2000)

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