2807-30-9 Usage
Chemical Properties
oily colourless odourless liquid
General Description
Liquid; colorless; mild, rancid odor; floats and mixes with water.
Reactivity Profile
Ethers, such as 2-PROPOXYETHANOL can act as bases. They form salts with strong acids and addition complexes with Lewis acids. The complex between diethyl ether and boron trifluoride is an example. Ethers may react violently with strong oxidizing agents. In other reactions, which typically involve the breaking of the carbon-oxygen bond, ethers are relatively inert.
Health Hazard
VAPOR: Irritating eyes and nose. LIQUID: Can cause corneal damage. INHALATION: Can cause toxic effects. SKIN: Contact can cause toxic effects.
Fire Hazard
Combustible: Carbon dioxide and carbon monoxide may be produced in a fire.
Safety Profile
Moderately toxic by
ingestion and skin contact. Mildly toxic by
inhalation. An experimental teratogen.
Experimental reproductive effects. Some
glycol ethers have dangerous human
reproductive effects. A skin and severe eye
irritant. Flammable; can react with oxilzing
materials. When heated to decomposition it
emits acrid smoke and irritating fumes. See
also GLYCOL ETHERS.
Check Digit Verification of cas no
The CAS Registry Mumber 2807-30-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,0 and 7 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2807-30:
(6*2)+(5*8)+(4*0)+(3*7)+(2*3)+(1*0)=79
79 % 10 = 9
So 2807-30-9 is a valid CAS Registry Number.
InChI:InChI=1/C6H14O.C2H6O2/c1-3-5-7-6-4-2;3-1-2-4/h3-6H2,1-2H3;3-4H,1-2H2
2807-30-9Relevant articles and documents
PRODUCTION OF HYDROXY ETHER HYDROCARBONS BY LIQUID PHASE HYDROGENOLYSIS OF CYCLIC ACETALS OR CYCLIC KETALS
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Page/Page column 8, (2013/02/28)
A liquid phase hydrogenolysis of acetal compounds such as cyclic acetals and cyclic ketals are fed to a reaction zone and reacted in the presence of a noble metal catalyst supported on a carbon or silica support to make hydroxy ether mono-hydrocarbons in high selectivity, without the necessity to use acidic co-catalysts such as phosphorus containing acids or stabilizers such as hydroquinone.
