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121669-46-3

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121669-46-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 121669-46-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,6,6 and 9 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 121669-46:
(8*1)+(7*2)+(6*1)+(5*6)+(4*6)+(3*9)+(2*4)+(1*6)=123
123 % 10 = 3
So 121669-46-3 is a valid CAS Registry Number.

121669-46-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name potassium salt of uroxanate

1.2 Other means of identification

Product number -
Other names dipotassium uroxanate

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:121669-46-3 SDS

121669-46-3Upstream product

121669-46-3Downstream Products

121669-46-3Relevant articles and documents

THE MECHANISM FOR THE CONVERSION OF URIC ACID INTO UROXANATE AND ALLANTOIN A NEW BASE-INDUCED 1,2-CARBOXYLATE SHIFT

Poje, M.,Sokolic-Maravic, Lea

, p. 6723 - 6728 (2007/10/02)

Alkaline permanganate oxidation of uric acid (1), particularly the late stages of the transformation into uroxanate (7) and allantoin (3), was studied by means of isotope-position labelling.A clear-cut degradation procedure developed for distinguishing among carbonyl and α-aminal carbon atoms in these products demonstrated conclusively that the carboxylic carbon of 7 and the 4-carbonyl carbon of 3 have their origin in C(5) of uric acid (1).None of the mechanisms that have been proposed for this reaction would have predicted this result.Isotope-labelling evidence, in combination with other data, revealed the sequence of events and identities of species involved in oxidative transformation of 1; the carbon-skeleton rearrangement of the first transient intermediate 4 must occur by a 1,2-carboxylate shift to give allanatoin-5-carboxylate (6) which either decarboxylates to allantoin (3) or else undergoes hydrolytic ring opening to uroxanate (7).

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