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99-16-1

99-16-1

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99-16-1 Usage

Chemical Properties

White Solid

Uses

An metabolic intermediate in nucleic acid metabolism.

Definition

ChEBI: A member of the class of ureas that consists of acetic acid in which the two methyl hydrogens are replaced by carbamoylamino groups respectively.

Check Digit Verification of cas no

The CAS Registry Mumber 99-16-1 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 9 and 9 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 99-16:
(4*9)+(3*9)+(2*1)+(1*6)=71
71 % 10 = 1
So 99-16-1 is a valid CAS Registry Number.
InChI:InChI=1/C4H8N4O4/c5-3(11)7-1(2(9)10)8-4(6)12/h1H,(H,9,10)(H3,5,7,11)(H3,6,8,12)

99-16-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name allantoic acid

1.2 Other means of identification

Product number -
Other names Allantursaeure

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:99-16-1 SDS

99-16-1Relevant articles and documents

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Fosse,Brunel,de Graeve

, (1929)

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Polar compounds isolated from the leaves of albertisia delagoensis (menispermaceae)

Hawkes, Geoffrey E.,De Wet, Helene,Li, Jia

, p. 9153 - 9160 (2011)

Aqueous infusions of the leaves of the shrub Albertisia delagoensis (Menispermaceae) are used in South Africa in traditional Zulu medicine to alleviate a variety of symptoms, including fever, and intestinal problems. We report the analysis of such an aqueous extract using the HPLC-NMR technique. A number of polar compounds were identified, including proto-quercitol, nicotinic acid, allantoic acid, 3,4-dihydroxybenzoic acid, phthalic acid and the aporphine alkaloid derivative roemrefidine. Allantoic acid and roemrefidine have been fully characterised by 1H- and 13C-NMR and mass spectrometry. Earlier reports of antiplasmodial activity of roemrefidine and of A. delagoensis extracts are correlated with this study and with the antipyretic properties of neutral aqueous extracts.

On the degradation of puric and pyrimidine bases in the soil: aerobic degradation of uric acid.

DURAND

, p. 1687 - 1689 (2007/10/05)

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