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THIOUREA-14C is a radioactive isotope of thiourea, a compound with the formula (NH2)2CS, which is utilized in scientific research to investigate the behavior of thiourea in various biological and chemical processes. The 14C label on thiourea enables researchers to track its movement and transformation in living organisms and the environment, offering valuable insights into its interactions and potential impacts.

5022-68-4

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5022-68-4 Usage

Uses

Used in Scientific Research:
THIOUREA-14C is used as a tracer in scientific research for studying the behavior of thiourea in biological and chemical processes. The radioactive isotope allows for tracking its movement and transformation in living organisms and the environment, providing insights into its interactions and potential impacts.
Used in Environmental Fate Studies:
THIOUREA-14C is used as a research tool in environmental fate studies to understand how thiourea and related compounds interact with the environment, their degradation pathways, and their ultimate fate.
Used in Metabolism Studies:
THIOUREA-14C is employed in metabolism studies to investigate how thiourea is processed and metabolized within living organisms, contributing to the understanding of its biological activity and potential toxicity.
Used in Toxicity Studies:
THIOUREA-14C is utilized in toxicity studies to assess the potential harmful effects of thiourea and related compounds on living organisms, helping to determine safe exposure levels and environmental regulations.
Used in Synthesis of Organic Compounds:
Although not directly mentioned in the provided materials, THIOUREA-14C could potentially be used as a reagent in the synthesis of organic compounds, similar to its non-radioactive counterpart, allowing researchers to study the synthesis process and the behavior of the synthesized compounds in a controlled manner.
Used in Photographic Chemicals:
While not explicitly stated, THIOUREA-14C could be used in the development of photographic chemicals, where its radioactive properties might offer unique insights into the chemical reactions involved in photographic processes.
Used in Metal Surface Treatment:
THIOUREA-14C could be employed in the treatment of metal surfaces, providing a means to study the interaction of thiourea with metals and potentially improving surface treatments through a better understanding of the underlying chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 5022-68-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,2 and 2 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5022-68:
(6*5)+(5*0)+(4*2)+(3*2)+(2*6)+(1*8)=64
64 % 10 = 4
So 5022-68-4 is a valid CAS Registry Number.

5022-68-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name THIOUREA-14C

1.2 Other means of identification

Product number -
Other names tetraglycerol

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:5022-68-4 SDS

5022-68-4Upstream product

5022-68-4Relevant academic research and scientific papers

The synthesis of 5,7-dimethyl-1,2,4-triazolo[1,5a(14C)] pyrimidine-2-carbaldehyde from [14C]aminoguanidine: A key intermediate for the radiochemical GMP synthesis of a drug candidate

Rane, Anil M.,Klaas, Schildknegt

scheme or table, p. 257 - 260 (2011/05/06)

Hydrazination of barium [14C]cyanamide and hydrazinolysis of S-methylisothio[14C]urea were compared for their ability to efficiently prepare [14C]aminoguanidine bicarbonate. [ 14C]Aminoguanidine bicarbonate was converted in three steps to 5, 7-dimethyl-1,2,4-triazolo[1,5a(14C)]pyrimidine-2-carbaldehyde, a key radiochemical GMP starting material. Copyright

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