Molecular Weight 130142 Propargyl Alcohol, Used as chemical intermediate, Physical Form Clear Yellow Liquid, pH Value 10 - 20

Obtato the greatest extent competitive rate for propargyl alcohol unique substance identifier107, 19,, C3h4o, In terms of package size 100ml bottle. Introduction propargyl alcohol manifests as colorless hue, A transparent fluid containing a geranium, Like odor. Flash point 97 f. Vapors are heavier than air. Used to make other chemicals, As a corrosion inhibitor and a soil fumigant. Prop, 2, Yn, 1, Ol is a terminal acetylenic compound that is prop, 2, Yne substituted by a -OH group at position 1. It serves as a function of a saccharomyces cerevisiae metabolite and an antifungal agent. You will find it to be a terminal acetylenic compound, A volatile organic compound and a propynol. Uses designed to inhibit hydrogen embrittlement of steelas corrosion inhibitorsolvent stabilizerchemical intermediatelab reagentpropargyl alcohol serves the purpose of an inhibitor for the corrosion of steel by hydrochloric acidas a stabilizer in certain chlorinated hydrocarbon formulationsthe alcohol is an excellent rust inhibitor, Superior in this respect to allyl alcohol. It retains its rust, Inhibiting properties at intense climatic factors and therefore is utilized for oil drilling. Identification analytic laboratory methods epa method 8090. Gas chromatographic method for the identification of ppb levels of nitroaromatic and cyclic ketone compounds. Detection is achieved by an electron capture detector ecd for dinitrotoluenes or a flame ionization detector fid for the other compounds amenable to this method. For 2, Propyn, 1, Ol, The method detection limit isn't regarded as given. Precision and method accuracy were found to be directly associated with the concentration of the analyte and essentially independent of the sample matrix. Epa method 8250. Packed column gas chromatography/mass spectrometry technique for the determination of semivolatile organic compounds in extracts prepared from every variety of solid waste matrices, Soil, And groundwater. This method is applicable to quantify most neutral, Acidic, And basic organic substances that consist of soluble in methylene chloride and capable of being eluted with derivatization as sharp peaks from a gas chromatographic packed column. Methods of manufacturing prepared by heating beta, Bromoallyl alcohol with concentrated koh from formaldehyde and sodium acetylide from epichlorohydrin, Sodium from acetylene and formaldehyde. Derived from acetylene by high, Pressure synthesis. Formed as a byproduct ~5% in the butynediol synthesis from acetylene and formaldehyde. Copper acetylide serves as catalyst. Pharmacology and biochemistryabsorption, Distribution and excretion propargyl alcohol is quickly distributed and excreted following an iv dose. The majority of the radioactivity 14 c, Labeled test material was excreted in the urine and as carbon dioxide in the breath of both rats and mice. Oral dosing resulted in a similar rapid but slower than after iv dosing with the, Excretion pattern bulk of radioactivity being excreted in the urine and exhaled carbon dioxide. Metabolism/metabolites while oxidative metabolism of low molecular weight primary alcohols is generally catalyzed by propargyl alcohol, Alcohol dehydrogenase is regarded as fairly poor substrate for this enzyme. Bovine liver catalase was used, To measure the rate of oxidative bioactivation of propargyl alcohol to 2, Propyn, L, Al. It was found the rate to be higher than predicted and hypothesized that the oxidative biotransformation of propargyl alcohol to the more reactive alpha, Beta, Unsaturated aldehyde by liver catalase might be the initial step in propargyl alcohol induced liver injury.