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1194-23-6

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1194-23-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1194-23-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,9 and 4 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1194-23:
(6*1)+(5*1)+(4*9)+(3*4)+(2*2)+(1*3)=66
66 % 10 = 6
So 1194-23-6 is a valid CAS Registry Number.

1194-23-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5,6-dihydro-6-hydroxyuracil

1.2 Other means of identification

Product number -
Other names 5-hydro-6-hydroxy uracil

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1194-23-6 SDS

1194-23-6Downstream Products

1194-23-6Relevant articles and documents

RADIOLYSIS OF DIHYDROURACIL AND DIHYDROTHYMINE IN AQUEOUS SOLUTIONS CONTAINING OXYGEN; FIRST- AND SECOND-ORDER REACTIONS OF THE ORGANIC PEROXYL RADICALS; THE ROLE OF ISOPYRIMIDINES AS INTERMEDIATES

Al-Sheikhly, Mohamed I.,Hissung, Alfred,Schuchmann, Heinz-Peter,Schuchmann, Man Nien,Sonntag, Clemens von,et al.

, p. 601 - 608 (2007/10/02)

The nature and yields of the products of radiolysis of aqueous solutions of dihydrouracil containing both N2O and O2 strongly depend on pH and dose rate.At a dose rate of 0.3 Gy s-1 and at pH 3, the major products are barbituric acid (G 2.4), labile material (G 2.8), and uracil (G 0.1).The labile material is converted into uracil upon treatment with acid and is largely composed of 5,6-dihydro-6-hydroxyuracil.At pH 7 barbituric acid is absent and uracil becomes the major product (G 4.5); some labile material is also formed (G 0.7).At pH 5 the pattern of the product distribution changes as a function of dose rate.With increasing dose r ate G(uracil) decreases whereas G(barbituric acid) increases.The predominant radical formed in the dihydrouracil system is the 6-peroxyl radical, and it has been found, using pulse radiolysis with both optical and conductometric detection, that this peroxyl radical can eliminate O2-. to give uracil via an unstable isomeric form of the pyrimidine (isouracil).The elimination is base-catalysed so that, under alkaline conditions, uracil is the major radiolysis product.At lower pH, and also at higher dose rates, bimolecular decay of the peroxyl radical competes with the O2-. elimination process, barbituric acid being a specific product of the bimolecular decay route.The mechanism of these processes are discussed.Irradiation of dihydrothymine-N2O-O2 solutions gave similar results.

Analysis of Radiolysis Products of Aqueous Uracil + N2O Solutions

Ali, Khondoker M. Idris,Scholes, George

, p. 449 - 456 (2007/10/02)

Various products from the irradiation of solutions of uracil+N2O with 60Co gamma rays were separated by paper chromatographic technique using 14C labelled materials.Identity of the isolated products was investigated by spectrophotometric and kinetic decomposition studies.Thus at least eight radiolytic products of uracil such as cis- and trans-uracil glycols, 5-hydroxy-6-hydro and 6-hydroxy-5-hydro compounds, isobarbituric acid and three dimeric products were identified.Yields of these products were determined at different pH values; a good material mass balance was achieved; the mechanism involved is discussed.

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