Chemical structure of 1,1,-Bis (4-Chlorophenyl)-2,2,2-Trichloroethane 4,4'-DTT | 50-29-3
SKU: S1349

4,5-Diamino-6-hydroxy-2-mercapto pyrimidine | 1004-76-8 |Sarcham Labs

SKU: S1349

Description

PubChem CID : 1201437

 

SPECIFICATION

AppearanceN/A
Content of ZincN/A
Boiling PointN / A
Melting PointN/A
Vapor PressureN/A
% Volatile by WeightN/A
Solubility in WaterN/A
DensityN/A
pH of Liquid, Typical (10% soln)N/A
Specific Gravity ApproxN/A
OdorN/A
pHN/A
Flash PointN/A
Ignition temperatureN/A
Lower exposure limitN/A
Upper exposure limitN/A

Safety Information

Classification of the substance or mixture

GHS Label elements, including precautionary statements

Hazards not otherwise classified (HNOC) or not covered by GHS

 

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4,5-Diamino-6-hydroxy-2-mercapto pyrimidine | 1004-76-8 FAQs

Applied in medicines, chemical synthesis, and industry, 4,5 diamino 6 hydroxy 2 mercapto pyrimidine are heterocyclic compounds. Its unique functional groups improve its reactivity, hence it is a useful ingredient in certain compositions.

C4H7N5OS is the 4,5 diamino 6 hydroxy 2 mercapto pyrimidine chemical formula. Amino, hydroxyl, and mercapto groups are included in this molecular structure to affect its reactivity and compatibility in certain chemical uses.

A pyridine ring with amino, hydroxyl, and mercapto groups positioned precisely forms the 4,5 diamino 6 hydroxy 2 mercapto pyrimidine. These functional groups support its solubility, stability, and chemical characteristics.

Pharmaceutical research, chemical synthesis, and industrial formulations all benefit from 4,5 diamino 6 hydroxy 2 mercapto pyrimidine. Its special molecular characteristics make it possible for sophisticated chemical operations and creative material creation.

Stored in a cool, dry place free from moisture and direct sunlight, 4,5 diamino 6 hydroxy 2 mercapto pyrimidine should be Correct handling practices, including protective equipment, to guarantee safety and preserve compound stability.