N, n-dimethylurea (1,3-dimethylurea) is a chemical compound with the molecular formula C4H8N2O.
N, n-dimethylurea (1,3-dimethylurea) belongs to the class of compounds known as ureas, characterized by the presence of the urea functional group.
N, n-dimethylurea (1,3-dimethylurea) features two methyl groups attached to separate nitrogen atoms within the urea structure.
Its molecular structure consists of a central urea moiety with two methyl substituents.
CAS Number: 96-31-1
EC Number: 202-498-7
APPLICATIONS
N, n-dimethylurea (1,3-dimethylurea) may find application as a reagent in the synthesis of complex organic molecules.
Its chemical structure could contribute to the design of nitrogen-rich polymers with specific properties.
In certain catalytic processes, N, n-dimethylurea (1,3-dimethylurea) might serve as a substrate or ligand.
N, n-dimethylurea (1,3-dimethylurea)'s solubility characteristics could be advantageous in specific solvent systems.
N, n-dimethylurea (1,3-dimethylurea) may be explored for its potential as a building block in pharmaceutical research.
Its participation in hydrogen bonding interactions may be of interest in supramolecular chemistry studies.
N, n-dimethylurea (1,3-dimethylurea) might have applications in the development of specialty coatings or adhesives.
In agricultural research, N, n-dimethylurea (1,3-dimethylurea) could be investigated for its effects on plant growth or as a potential fertilizer component.
The unique reactivity of N, n-dimethylurea (1,3-dimethylurea) might make it suitable for certain polymerization reactions.
Research into its behavior under different temperature and pressure conditions may reveal new applications.
N, n-dimethylurea (1,3-dimethylurea) could be explored as a potential precursor in the synthesis of heterocyclic compounds.
Its presence in reaction mixtures may impact the selectivity of certain chemical transformations.
In the field of materials science, N, n-dimethylurea (1,3-dimethylurea) might be incorporated into the design of novel materials.
Researchers might investigate its use in the development of specialty resins or coatings.
N, n-dimethylurea (1,3-dimethylurea) could be evaluated for its role in catalyzing specific chemical reactions.
N, n-dimethylurea (1,3-dimethylurea)'s potential to form complexes with metal ions may be explored in coordination chemistry studies.
Its stability under certain conditions could make it suitable for inclusion in specific formulations.
In medicinal chemistry, N, n-dimethylurea (1,3-dimethylurea) may be examined for potential pharmacological properties.
N, n-dimethylurea (1,3-dimethylurea)'s solubility characteristics might be advantageous in the formulation of certain pharmaceutical products.
N, n-dimethylurea (1,3-dimethylurea) may be studied for its potential as a flame retardant in certain materials.
In the realm of environmental chemistry, its behavior in aqueous systems could be investigated.
Its use in specialty chemical processes may be explored for the development of new materials.
Researchers might assess its impact on reaction kinetics and product distribution in various chemical reactions.
N, n-dimethylurea (1,3-dimethylurea)'s potential as a reagent in asymmetric synthesis could be of interest in organic chemistry.
Its interaction with specific enzymes or catalysts might be examined for potential biotechnological applications.
N, n-dimethylurea (1,3-dimethylurea)'s solubility properties may make it suitable for inclusion in certain formulations of specialty inks or dyes.
In the realm of nanotechnology, the compound might be investigated for its role in the synthesis of nanomaterials with unique properties.
Its potential as a stabilizing agent in the formulation of certain emulsions or dispersions could be explored in the cosmetic industry.
N, n-dimethylurea (1,3-dimethylurea) may be considered as a potential co-catalyst in certain chemical reactions to enhance reaction rates.
Its ability to form complexes with metal ions may find application in analytical chemistry for selective metal ion detection.
N, n-dimethylurea (1,3-dimethylurea) could be examined for its influence on the crystallization behavior of certain materials in materials science research.
Researchers might investigate N, n-dimethylurea (1,3-dimethylurea)'s behavior in ionic liquids for potential applications in green chemistry.
Its role as a potential building block in the design of supramolecular structures could be explored in molecular assembly studies.
N, n-dimethylurea (1,3-dimethylurea) may be assessed for its compatibility with specific polymers in the development of specialty polymer blends.
N, n-dimethylurea (1,3-dimethylurea)'s interaction with certain biomolecules could be investigated for applications in bioorganic chemistry.
In the field of medicinal chemistry, its potential as a ligand in the design of metallopharmaceuticals might be explored.
N, n-dimethylurea (1,3-dimethylurea) might be considered as a potential corrosion inhibitor in the formulation of specialty coatings.
N, n-dimethylurea (1,3-dimethylurea)'s stability under specific environmental conditions could find application in soil remediation processes.
Its behavior as a potential chelating agent may be studied for applications in wastewater treatment processes.
N, n-dimethylurea (1,3-dimethylurea)'s reactivity might be harnessed for its potential use in the synthesis of specialty fine chemicals.
N, n-dimethylurea (1,3-dimethylurea) could be evaluated for its impact on the rheological properties of certain formulations in the cosmetics industry.
In the development of smart materials, researchers might explore its responsiveness to external stimuli.
N, n-dimethylurea (1,3-dimethylurea) might be considered for its potential role as a template in the synthesis of porous materials.
N, n-dimethylurea (1,3-dimethylurea)'s use as a potential precursor in the synthesis of conducting polymers may be investigated.
Its presence in certain reaction mixtures may influence the regioselectivity of certain chemical reactions.
Researchers might explore its potential as a reducing agent in the synthesis of nanoparticles.
N, n-dimethylurea (1,3-dimethylurea)'s participation in certain organometallic reactions might be studied for applications in organometallic chemistry.
N, n-dimethylurea (1,3-dimethylurea)'s unique properties could be harnessed for applications in the development of specialty adhesives.
Its compatibility with specific organic compounds may find applications in the formulation of specialty lubricants.
N, n-dimethylurea (1,3-dimethylurea) might be investigated for its potential as a reagent in the synthesis of functionalized organic molecules for material science applications.
N, n-dimethylurea (1,3-dimethylurea)'s compatibility with certain resins may make it suitable for incorporation into specialty composite materials.
In the field of energy storage, N, n-dimethylurea (1,3-dimethylurea) could be explored for its potential use in the design of advanced battery electrolytes.
Its interaction with specific catalysts may open avenues for exploring its role in catalytic asymmetric reactions in organic synthesis.
N, n-dimethylurea (1,3-dimethylurea) might be studied for its potential as a template in the synthesis of zeolites with controlled porosity.
Its solubility characteristics could be advantageous in the formulation of certain types of agricultural chemicals or fertilizers.
N, n-dimethylurea (1,3-dimethylurea) may find application in the development of specialty lubricating oils due to its chemical stability.
Researchers might investigate its potential as a precursor in the synthesis of nitrogen-rich energetic materials.
N, n-dimethylurea (1,3-dimethylurea) could be explored for its use in the creation of controlled-release formulations in the pharmaceutical industry.
Its potential as a stabilizer in the formulation of certain polymer blends may be of interest in plastics manufacturing.
In the realm of water treatment, the compound might be considered for its chelating properties in metal ion removal processes.
N, n-dimethylurea (1,3-dimethylurea)'s behavior under specific temperature and pressure conditions could find applications in high-pressure chemistry.
Its potential to form inclusion complexes may be explored for applications in drug delivery systems.
N, n-dimethylurea (1,3-dimethylurea) might be studied for its impact on the rheological behavior of certain polymer solutions in the cosmetics industry.
N, n-dimethylurea (1,3-dimethylurea)'s interaction with specific transition metals could be investigated for potential catalytic applications.
Researchers might explore its potential as a corrosion inhibitor in the formulation of coatings for metal surfaces.
Its use as a potential intermediate in the synthesis of specialty surfactants may find applications in the detergent industry.
N, n-dimethylurea (1,3-dimethylurea) could be investigated for its potential role in the synthesis of nitrogen-doped carbon materials.
N, n-dimethylurea (1,3-dimethylurea)'s reactivity under controlled conditions might be harnessed for applications in organometallic chemistry.
Its ability to form complexes with certain guest molecules may be explored for gas storage applications.
N, n-dimethylurea (1,3-dimethylurea) might be studied for its potential as a stabilizing agent in the formulation of colloidal suspensions.
In the field of materials science, its role in the synthesis of metal-organic frameworks (MOFs) may be investigated.
N, n-dimethylurea (1,3-dimethylurea)'s participation in certain chemical reactions may be explored for applications in green chemistry.
Researchers might study its potential as a co-catalyst in the development of sustainable chemical processes.
N, n-dimethylurea (1,3-dimethylurea)'s reactivity toward specific functional groups could be explored for applications in organic synthesis.
N, n-dimethylurea (1,3-dimethylurea)'s unique properties might find applications in the creation of stimuli-responsive materials for advanced technologies.
N, n-dimethylurea (1,3-dimethylurea)'s potential role as a phase-transfer catalyst may find applications in facilitating reactions between immiscible phases.
In the realm of polymer science, N, n-dimethylurea (1,3-dimethylurea) might be explored for its influence on the crystallization behavior of polymeric materials.
Its compatibility with certain inorganic salts may make it suitable for use in the formulation of electrolytes for specific applications.
N, n-dimethylurea (1,3-dimethylurea) could be studied for its potential as a nitrogen source in the synthesis of nitrogen-doped carbon nanomaterials.
N, n-dimethylurea (1,3-dimethylurea)'s participation in specific redox reactions may open avenues for its use in electrochemical applications.
Researchers might explore its potential as a stabilizing agent in the formulation of nanoparticle dispersions for various applications.
In the field of sensors and detection, N, n-dimethylurea (1,3-dimethylurea)'s reactivity toward specific analytes might be harnessed for sensing applications.
Its potential role as a ligand in coordination chemistry may find applications in the design of novel metal complexes.
N, n-dimethylurea (1,3-dimethylurea) could be investigated for its impact on the viscosity of certain fluid systems in industrial processes.
N, n-dimethylurea (1,3-dimethylurea)'s solubility characteristics may be advantageous in the formulation of specialty inks for specific printing applications.
Its interaction with specific polymers might be explored for potential applications in the modification of polymer surfaces.
N, n-dimethylurea (1,3-dimethylurea)'s potential as a complexing agent for certain metal ions may be relevant in analytical chemistry applications.
N, n-dimethylurea (1,3-dimethylurea) could be studied for its potential use as a sacrificial reagent in specific chemical transformations.
In the realm of catalysis, N, n-dimethylurea (1,3-dimethylurea) might be considered as a co-catalyst in the development of asymmetric catalytic reactions.
Researchers might investigate its role as a precursor in the synthesis of heterocyclic compounds with unique properties.
N, n-dimethylurea (1,3-dimethylurea)'s potential as a template in the formation of metal-organic frameworks (MOFs) may have applications in gas storage.
N, n-dimethylurea (1,3-dimethylurea)'s compatibility with specific organic solvents could find applications in the design of novel solvent systems.
Its use as a potential reducing agent might be explored for applications in the synthesis of metal nanoparticles.
N, n-dimethylurea (1,3-dimethylurea)'s potential in the development of environmentally friendly processes may be relevant to green chemistry initiatives.
N, n-dimethylurea (1,3-dimethylurea)'s potential as a nitrogen source in the synthesis of specialty polymers might find applications in material science.
Researchers might explore its use in the formulation of controlled-release fertilizers for agricultural applications.
N, n-dimethylurea (1,3-dimethylurea)'s interaction with specific additives might be investigated for potential applications in the enhancement of lubricant properties.
Its compatibility with certain biodegradable polymers may make it suitable for use in environmentally friendly materials.
N, n-dimethylurea (1,3-dimethylurea) could be explored for its role in the synthesis of nitrogen-containing pharmaceutical intermediates.
N, n-dimethylurea (1,3-dimethylurea)'s participation in certain oxidation reactions may find applications in the development of oxidative coupling processes.
DESCRIPTION
N, n-dimethylurea (1,3-dimethylurea) is a chemical compound with the molecular formula C4H8N2O.
N, n-dimethylurea (1,3-dimethylurea) belongs to the class of compounds known as ureas, characterized by the presence of the urea functional group.
N, n-dimethylurea (1,3-dimethylurea) features two methyl groups attached to separate nitrogen atoms within the urea structure.
Its molecular structure consists of a central urea moiety with two methyl substituents.
N, n-dimethylurea (1,3-dimethylurea) has a linear molecular geometry, with the nitrogen atoms forming a bridge between the two methyl groups.
N, n-dimethylurea (1,3-dimethylurea) exhibits characteristics of both urea and methylated derivatives, influencing its reactivity and properties.
N, n-dimethylurea (1,3-dimethylurea) is colorless, and its physical state can vary depending on temperature and pressure conditions.
N, n-dimethylurea (1,3-dimethylurea) is synthesized through specific chemical reactions involving urea and methylating agents.
N, n-dimethylurea (1,3-dimethylurea) is used in various industrial applications, including as a reagent in chemical synthesis.
The presence of methyl groups enhances the compound's solubility in certain organic solvents.
N, n-dimethylurea (1,3-dimethylurea) may participate in hydrogen bonding interactions due to the presence of amide functional groups.
N, n-dimethylurea (1,3-dimethylurea) has specific applications in organic chemistry as a building block for the synthesis of more complex molecules.
Its molecular weight is approximately 100.12 grams per mole.
The chemical structure of N, N-dimethylurea imparts unique chemical and physical properties, influencing its behavior in reactions.
N, n-dimethylurea (1,3-dimethylurea) can act as a reactant in the preparation of various nitrogen-containing organic compounds.
N, n-dimethylurea (1,3-dimethylurea)'s stability and reactivity depend on environmental factors and reaction conditions.
N, n-dimethylurea (1,3-dimethylurea) may be subject to certain regulatory considerations due to its use in chemical processes.
Its presence in a reaction mixture can influence reaction kinetics and product distribution.
In certain contexts, N, n-dimethylurea (1,3-dimethylurea) may serve as a model compound for theoretical studies on molecular interactions.
N, n-dimethylurea (1,3-dimethylurea)'s chemical behavior can be explored in the context of hydrogen bonding and steric effects.
Researchers may study its behavior as a substrate in enzymatic or catalytic reactions.
N, n-dimethylurea (1,3-dimethylurea)'s chemical versatility contributes to its utility in various laboratory settings.
N, n-dimethylurea (1,3-dimethylurea) is important for researchers and chemists to consider the compound's properties when designing experiments.
The synthesis of N, n-dimethylurea (1,3-dimethylurea) can involve the use of specific catalysts and reaction conditions.
Understanding the reactivity and properties of N, n-dimethylurea (1,3-dimethylurea) is crucial for its effective utilization in chemical processes.
PROPERTIES
Physical Properties:
Molecular Formula: C4H8N2O
Molecular Weight: Approximately 100.12 g/mol
Appearance: Typically a colorless or white crystalline solid.
Melting Point: The melting point of N, N-dimethylurea is influenced by factors such as purity and crystalline form. It is generally reported in the range of 155-160°C.
Chemical Properties:
Solubility: The compound is usually soluble in polar solvents, including water and some organic solvents.
Reactivity:
Reactivity with Metals: N, N-dimethylurea may form complexes with certain metal ions, and its reactivity can be influenced by the presence of metal catalysts.
Hydrogen Bonding: The amide functional groups in the urea moiety may participate in hydrogen bonding interactions.
FIRST AID
Inhalation:
Move to Fresh Air:
If inhaled, move the affected person to an area with fresh air.
Ensure proper breathing.
If breathing difficulties persist, seek immediate medical attention.
Skin Contact:
Remove Contaminated Clothing:
Quickly and gently remove contaminated clothing, including shoes.
Wash Skin Thoroughly:
Wash the affected skin area thoroughly with mild soap and water.
Rinse for at least 15 minutes.
Seek Medical Attention:
If irritation, redness, or other symptoms persist, seek medical attention.
Eye Contact:
Rinse Eyes Immediately:
Immediately rinse the eyes with gently flowing lukewarm water.
Ensure thorough rinsing for at least 15 minutes, holding eyelids open.
Seek Medical Attention:
Seek immediate medical attention if irritation, redness, or pain persists.
Ingestion:
Do Not Induce Vomiting:
If swallowed, do not induce vomiting.
Rinse the mouth and drink plenty of water if the person is conscious.
Seek Medical Attention:
Seek immediate medical attention.
HANDLING AND STORAGE
Handling:
Personal Protection:
Wear appropriate personal protective equipment (PPE), including gloves and safety goggles, to prevent skin and eye contact.
Ventilation:
Use in a well-ventilated area to minimize inhalation exposure.
Consider local exhaust ventilation if handling the substance in enclosed spaces.
Avoidance of Contact:
Avoid skin and eye contact.
Do not ingest the substance.
Wash hands thoroughly after handling.
Spill and Leak Procedures:
In the event of a spill, contain and collect the material using appropriate absorbent materials.
Prevent the substance from entering waterways or sewer systems.
Follow established spill response procedures in accordance with local regulations.
Handling Precautions:
Avoid generating dust, aerosols, or mists.
Do not eat, drink, or smoke while handling the substance.
Implement good industrial hygiene practices in the workplace.
Static Electricity:
Take measures to prevent the buildup of static electricity.
Ground equipment and containers to dissipate static charges.
Compatibility:
Ensure compatibility with other substances and materials used in the workplace.
Avoid contact with incompatible materials.
Storage:
Storage Location:
Store N, N-dimethylurea in a cool, dry, and well-ventilated area.
Keep away from direct sunlight and heat sources.
Temperature:
Store at temperatures recommended by the manufacturer or within specified temperature ranges.
Avoid extreme temperature fluctuations.
Container Integrity:
Use containers made of materials compatible with N, N-dimethylurea.
Ensure containers are tightly sealed to prevent contamination and evaporation.
Separation from Incompatible Materials:
Store away from incompatible substances, such as strong acids, bases, and oxidizing agents.
Spill Containment:
Provide spill containment measures, such as secondary containment, to prevent environmental contamination.
Handling of Bulk Quantities:
For bulk quantities, use appropriate storage vessels and ensure compliance with local regulations.
SYNONYMS
1,3-Dimethylurea
Dimethylurea
N,N-Dimethylcarbamide
1,3-Dimethylcarbamide
Dimethylurea (1,3-DMU)
N,N-Dimethylurea
Dimethylurea (1,3)
NSC 21989
BRN 1209243
EINECS 209-819-0
AC1Q78GE
AI3-00957
1,3-Dimethylurea, Technical Grade
MFCD00008022
NSC21989
3-Dimethylurea
1,3-DIMETHYLUREA, 98%
N,N-Dimethyl Urea
1,3-DIMETHYLUREA, REAGENTPLUS, 99%
1,3-DIMETHYLUREA, 97%
N,N-dimethylcarbamide
1,3-Dimethylurea, 99%
N,N-DIMETHYLUREA, ANHYDROUS
1,3-Dimethylurea, purum, ≥99.0% (GC)
Dimethylurea (DMU)
1,3-Dimethylcarbamoylurea
Dimethylurea (3-DMU)
Carbamoyl-N,N-dimethylurea
3-Dimethylcarbamoylurea
Carbamide, N,N-dimethyl-
Dimethylcarbamoylurea
N,N-Dimethylurea
1,3-Bis(methylcarbamoyl)urea
1,3-Dimethylurea (DMU)
NSC 62944
Urea, 1,3-bis(methylcarbamoyl)-
N,3-Dimethylurea
1,3-Dimethylcarbamide
1,3-Dimethylcarbonylurea
N,3-Dimethylcarbamoylurea
1,3-Dimethylurea (DMU)
N,N-Dimethylcarbonylurea
N,N'-Dimethylurea
Dimethylcarbamoylcarbamide
3-Dimethylurea
1,3-Dimethylurea, anhydrous
Carbamide, 1,3-bis(methylcarbamoyl)-
1,3-Dimethylurea, BioReagent, for molecular biology
1,3-Dimethylurea, 99+%
Urea, 1,3-bis(methylcarbamoyl)-, hydrochloride
Dimethylcarbamoylurea
1,3-Dimethylcarbamoylurea
Carbamide, 1,3-dimethyl-
1,3-Dimethylcarbonylurea
Dimethylcarbamide
Carbamoyl-N,N-dimethyl urea
N,N-Dimethylcarbamoylurea
3-Dimethylcarbamide
1,3-Dimethylurea, anhydrous, 99%
1,3-Dimethylurea, for HPLC, 99%
1,3-Dimethylurea, certified reference material
1,3-Dimethylurea, solution 1.0 M in THF
1,3-Dimethylurea, solution 1.0 M in acetone
1,3-Dimethylurea, puriss. p.a., Reag. Ph. Eur.
N,N-Dimethylurea, anhydrous, 99%
N,N-Dimethylurea, analytical standard
Dimethylurea, 97%
1,3-Dimethylurea, PharmaGrade, Manufactured under appropriate GMP controls for pharma or biopharmaceutical production
1,3-Dimethylurea, Vetec™ reagent grade, 98%
N,N-Dimethylurea, anhydrous, 98+%
1,3-Dimethylurea, pharmaceutical secondary standard; traceable to USP
N,N-Dimethylurea, BioUltra, ≥99.0% (T)
1,3-Dimethylurea, United States Pharmacopeia (USP) Reference Standard
N,N-Dimethylurea, purum, ≥98% (HPLC)
1,3-Dimethylurea, SAJ special grade, ≥97.0%
