1859-08-1 Usage
Uses
Used in Alcoholic Beverages:
ETHYL-D5 ALCOHOL is used as a component in alcoholic beverages for [providing the desired taste and alcohol content], in suitable dilutions.
Used in Laboratory and Industry:
ETHYL-D5 ALCOHOL is used as a solvent in [facilitating various chemical reactions and processes], in both laboratory and industrial settings.
Used in the Manufacture of Denatured Alcohol:
ETHYL-D5 ALCOHOL is used as an ingredient in [producing denatured alcohol], which is essential for non-beverage purposes.
Used in Pharmaceuticals:
ETHYL-D5 ALCOHOL is used as a component in [various pharmaceutical formulations], due to its compatibility and effectiveness in drug delivery.
Used in Perfumery:
ETHYL-D5 ALCOHOL is used as a base or solvent in [perfume production], for its ability to dissolve and carry fragrance components.
Used in Organic Synthesis:
ETHYL-D5 ALCOHOL is used as a reagent in [organic synthesis], contributing to the formation of various organic compounds.
Used as an Antiseptic:
ETHYL-D5 ALCOHOL is used as an antiseptic for [disinfecting and preventing infection], thanks to its antimicrobial properties.
Used in Time-of-Flight Secondary Ion Mass Spectrometry (TOF-SIMS) Tracer Method:
ETHYL-D5 ALCOHOL is used as a tracer in [assessing the boundary lubricating behaviors of boundary lubricating films], in the TOF-SIMS tracer method.
Used in Stable Isotope Gas Chromatography-Mass Spectrometry Technique:
ETHYL-D5 ALCOHOL is used as a reference compound in [quantifying ethyl-d5 alcohol and ethyl alcohol in serum], by employing the stable isotope gas chromatography-mass spectrometry technique.
Check Digit Verification of cas no
The CAS Registry Mumber 1859-08-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,5 and 9 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1859-08:
(6*1)+(5*8)+(4*5)+(3*9)+(2*0)+(1*8)=101
101 % 10 = 1
So 1859-08-1 is a valid CAS Registry Number.
InChI:InChI=1/C2H6O/c1-2-3/h3H,2H2,1H3/i1D3,2D2
1859-08-1Relevant academic research and scientific papers
Regioselective deuteration of alcohols in D2O catalysed by homogeneous manganese and iron pincer complexes
Kar, Sayan,Goeppert, Alain,Sen, Raktim,Kothandaraman, Jotheeswari,Surya Prakash
supporting information, p. 2706 - 2710 (2018/07/05)
We report a convenient and cost-effective protocol for the regioselective deuteration of primary and secondary alcohols using Earth abundant homogeneous first row transition metal pincer catalysts. D2O is utilized as both a deuterium source and a solvent, allowing for a benign inexpensive process. Depending on the metal selected (Mn or Fe), a high degree of deuterium incorporation was observed selectively either at the α and β position (Mn) or exclusively at the α position (Fe), for primary alcohols. This simple, efficient, and cost-effective protocol for alcohol C-H bond deuteration constitutes a powerful tool for the large scale synthesis of deuterated molecules.
Reactions of OH Radicals with Methanethiol, Dimethyl Sulfide, and Dimethyl Disulfide in Air
Hatakeyama, Shiro,Akimoto, Hajime
, p. 2387 - 2395 (2007/10/02)
Photooxidations of CH3SH, CH3SSCH3 (DMDS), and CH3SCH3 (DMS) in air were performed with alkyl nitrites as sources of OH radicals.Sulfur-containing final products are SO2, CH3SO3H (methanesulfonic acid), and a little H2SO4 in all cases.CH3SH reacts with OH to form an adduct, which further reacts with alkyl nitrites to give CH3SNO (methyl thionitrite) and the corresponding alcohols.CH3S radical produced by photolysis of CH3SNO gives final products.DMDS also reacts with OH via addition followed by rapid cleavage of the S-S bond, resulting in CH3S and CH3SOH.Reaction of DMS with OH can be explained by both addition and abstraction.In both cases the CH3S radical is the main intermediate which produces final products.The reaction of the CH3S radical with O2 proceeds via addition and gives HCHO + SO2 or CH3SO3H as final products.The rate constant ratios of CH3S with NO and O2 were obtained to be ca. 2 x 1E3, which is about one-tenth of that for CH3O.
