07-5360
1,4-Dioxane
SAJ first grade
Synonym(s):
Diethylene oxide, Dioxane
Sign In to View Organizational & Contract Pricing.
Select a Size
Change View
About This Item
Empirical Formula (Hill Notation):
C4H8O2
CAS Number:
Molecular Weight:
88.11
PubChem Substance ID:
UNSPSC Code:
12352005
Beilstein/REAXYS Number:
102551
MDL number:
grade
SAJ first grade
vapor density
3 (vs air)
vapor pressure
27 mmHg ( 20 °C), 40 mmHg ( 25 °C)
assay
>99.0% (GC)
form
liquid
autoignition temp.
356 °F
expl. lim.
22 %
availability
available only in Japan
refractive index
n20/D 1.422 (lit.)
pH
6.0-8 (20 °C, 500 g/L)
bp
100-102 °C (lit.)
mp
10-12 °C (lit.)
density
1.034 g/mL at 25 °C (lit.)
SMILES string
C1COCCO1
InChI
1S/C4H8O2/c1-2-6-4-3-5-1/h1-4H2
InChI key
RYHBNJHYFVUHQT-UHFFFAOYSA-N
Still not finding the right product?
Explore all of our products under 1,4-Dioxane
signalword
Danger
hcodes
Hazard Classifications
Carc. 1B - Eye Irrit. 2 - Flam. Liq. 2 - STOT SE 3
target_organs
Respiratory system
supp_hazards
Storage Class
3 - Flammable liquids
wgk
WGK 3
flash_point_f
53.6 °F
flash_point_c
12 °C
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Huijiao Wang et al.
Journal of hazardous materials, 294, 90-98 (2015-04-12)
Degradation of 1,4-dioxane by ozonation, electrolysis, and their combined electro-peroxone (E-peroxone) process was investigated. The E-peroxone process used a carbon-polytetrafluorethylene cathode to electrocatalytically convert O2 in the sparged ozone generator effluent (O2 and O3 gas mixture) to H2O2. The electro-generated
Xiaohua Liu et al.
Biomaterials, 31(2), 259-269 (2009-09-29)
It remains a challenge to synthesize functional materials that can develop advanced scaffolding architectures for tissue engineering. In this study, a series of biodegradable amphiphilic poly(hydroxyalkyl (meth)acrylate)-graft-poly(l-lactic acid) (PHAA-g-PLLA) copolymers have been synthesized and fabricated into nano-fibrous scaffolds. These copolymers
Joshua J Pacheco et al.
Proceedings of the National Academy of Sciences of the United States of America, 111(23), 8363-8367 (2014-06-10)
Terephthalic acid (PTA), a monomer in the synthesis of polyethylene terephthalate (PET), is obtained by the oxidation of petroleum-derived p-xylene. There is significant interest in the synthesis of renewable, biomass-derived PTA. Here, routes to PTA starting from oxidized products of
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 07-5360-3-3L-J | 04061837740343 |
| 07-5360-5-500ML-J | 04061837740350 |