131970
1,4-Thioxane
98%
Synonym(s):
1,4-Oxathiane
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About This Item
Empirical Formula (Hill Notation):
C4H8OS
CAS Number:
Molecular Weight:
104.17
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
240-117-6
MDL number:
Product Name
1,4-Thioxane, 98%
InChI key
JBYHSSAVUBIJMK-UHFFFAOYSA-N
InChI
1S/C4H8OS/c1-3-6-4-2-5-1/h1-4H2
SMILES string
C1CSCCO1
assay
98%
form
liquid
refractive index
n20/D 1.5095 (lit.)
bp
147 °C/755 mmHg (lit.)
density
1.114 g/mL at 25 °C (lit.)
functional group
ether
thioether
Quality Level
Application
1,4-Thioxane (1,4-oxathiane) was used to study the growth and characterization of the vertically aligned zinc oxide (ZnO) nanowires.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
3 - Flammable liquids
wgk
WGK 2
flash_point_f
107.6 °F - closed cup
flash_point_c
42 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Regulatory Information
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S Hindley et al.
Journal of nanoscience and nanotechnology, 11(9), 8294-8301 (2011-11-22)
Vertically aligned zinc oxide (ZnO) nanowires (NWs) have been grown by liquid injection Metal Organic Chemical Vapour Deposition, using oxygen donor adducts of Me2Zn. The growth and characterisation of the nanowires grown using [Me2Zn(L)] where L = monodentate ethers, tetrahydrofuran
Xin Zhang et al.
Environmental science & technology, 43(3), 610-615 (2009-02-28)
The long-term fate of chemical weapon debris disposed of in the ocean some 50 years ago, now sinking into marine sediments and leaking into the ocean environment, is poorly known. Direct evidence exists showing chemical weapon agents actively being released
Michał Czub et al.
Marine environmental research, 161, 105077-105077 (2020-08-28)
Sulphur mustard (HD) was the most widely produced chemical warfare agent (CWA) in the history of chemical warfare (CW). Simultaneously, the loads of HD account as by far the largest fraction of the sea-dumped CW. Nowadays its presence in the
M W Ellzy et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 57(12), 2417-2432 (2002-01-05)
We present a detailed analysis of the structure and infrared spectra of 1,4-thioxane. The vibrational frequencies of the 1,4-thioxane molecule were analyzed using standard quantum chemical techniques. Frequencies were calculated at the MP2 and DFT levels of theory using the
Heidi Lees et al.
Electrophoresis, 38(7), 1075-1082 (2017-01-04)
In this study, novel, fast, and simple methods based on RP-HPLC and MEKC with DAD are developed and validated for the qualitative and quantitative determination of five cyclic sulfur mustard (HD) degradation products (1,4-thioxane, 1,3-dithiolane, 1,4-dithiane, 1,2,5-trithiepane, and 1,4,5-oxadithiepane) in
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