1,3-Dimethylurea (CAS 96-31-1) Market Size By Type, ...

The "1,3-Dimethylurea (CAS 96-31-1) market" decisions are mostly driven by resource optimization and cost-effectiveness. Demand and supply dynamics are revealed by market research, which supports the predicted growth at a 11.4% yearly from to .

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Exploring the Current and Future of the 1,3-Dimethylurea (CAS 96-31-1) Market

1,3-Dimethylurea (CAS 96-31-1) is an organic compound commonly used as a versatile building block in various chemical processes, particularly in the synthesis of agricultural products, pharmaceuticals, and polymers. Its unique properties make it valuable in the formulation of nitrogen fertilizers and other agrochemicals, contributing to enhanced agricultural productivity. The increasing demand for effective agricultural inputs and pharmaceutical intermediates has made the 1,3-Dimethylurea market significant, underpinning its role in supporting food security and healthcare.

The growth trajectory of the 1,3-Dimethylurea market is influenced by several factors, including rising agricultural needs and innovations in chemical formulations. The compound's market is expected to experience a positive Compound Annual Growth Rate (CAGR) from to , reflecting the compound's expanding applications and the growing emphasis on sustainable agriculture practices. This trend highlights the importance of 1,3-Dimethylurea in addressing future global demands in both agriculture and pharmaceuticals.

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Leading Market Players in the 1,3-Dimethylurea (CAS 96-31-1) Market

• Accela ChemBio
• AK Scientific
• Henan Tianfu Chemical
• Qingdao Hong Jin Chemical
• Jinan Great Chemical Industry
• Shijiazhuang Kunxiangda
• Nanjing Chemlin Chemical Industrial

The market for 1,3-Dimethylurea, a versatile chemical used in agricultural and pharmaceutical applications, is characterized by a competitive landscape with several key players. Among them, Accela ChemBio and AK Scientific are notable for their robust product portfolios and international distribution networks. Accela ChemBio has been focusing on expanding its production capacity to meet growing demand, particularly from the agricultural sector, while also investing in research to improve product efficacy. AK Scientific, on the other hand, emphasizes high-purity chemical manufacturing and has been witnessing steady growth due to increased demand from the pharmaceutical industry, positioning itself as a reliable supplier.

Henan Tianfu Chemical and Qingdao Hong Jin Chemical are also prominent in the market, with Henan Tianfu Chemical gaining traction through competitive pricing and a commitment to sustainability. Jinan Great Chemical Industry and Shijiazhuang Kunxiangda are leveraging regional advantages, catering primarily to local markets but showing potential for future expansion. As for sales revenues, while specific figures can be elusive, reports indicate that companies in this sector are expected to experience an annual growth rate of 5-7%, with the overall market projected to reach a valuation in excess of $100 million within the next few years, driven by increasing applications in various sectors.

1,3-Dimethylurea (CAS 96-31-1) Market Segmentation for period from to

The 1,3-Dimethylurea (CAS 96-31-1) Market Analysis by types is segmented into:

• Purity &#;98%
• Purity <98%

The market for 1,3-Dimethylurea, classified by purity levels, consists of two main segments: purity &#;98% and purity <98%. The &#;98% purity segment is typically sought after in high-quality applications, including pharmaceuticals and specialized chemical processes, where superior performance and reliability are essential. In contrast, the <98% purity segment caters to cost-sensitive industries or applications that do not require stringent purity standards, such as certain agricultural uses or basic research, providing varied pricing and consumption patterns.

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Market Applications The 1,3-Dimethylurea (CAS 96-31-1) Market Industry Research by Application is segmented into:

• Pharmaceutical Industry
• Textile Industry
• Others

1,3-Dimethylurea, with CAS 96-31-1, has diverse applications in various industries. In the pharmaceutical industry, it is used as a chemical intermediate and in drug formulation due to its beneficial properties. In the textile industry, it acts as a finishing agent, enhancing the fabric's performance and durability. Additionally, it finds use in agriculture as a fertilizer component and in plastics production, contributing to various manufacturing processes. Its versatility makes it valuable across multiple sectors.

Key Drivers and Barriers in the 1,3-Dimethylurea (CAS 96-31-1) Market

The 1,3-Dimethylurea market is driven by its applications in agriculture as a fertilizer and in pharmaceutical formulations, fostering demand for enhanced crop yields and innovative drug development. Increased adoption of precision farming techniques and the growth of the pharmaceutical sector further propel market expansion. However, challenges such as regulatory restrictions and environmental concerns complicate production. Innovative solutions include developing green synthesis methods and safer formulations, promoting biodegradable alternatives, and leveraging advanced technologies for sustainability. Collaborative efforts between industry stakeholders and regulators can also foster a balanced approach to growth while addressing environmental and safety issues effectively.

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Geographical Regional Spread of 1,3-Dimethylurea (CAS 96-31-1) Market

• North America: United States Canada
• Europe: Germany France U.K. Italy Russia
• Asia-Pacific: China Japan South Korea India Australia China Taiwan Indonesia Thailand Malaysia
• Latin America: Mexico Brazil Argentina Korea Colombia
• Middle East & Africa: Turkey Saudi Arabia UAE Korea

The market for 1,3-Dimethylurea (CAS 96-31-1) is influenced by various regional factors, including industrial demand, economic conditions, and demographic trends.

In North America, particularly in the United States and Canada, the market is driven by the chemical industry's growth and the increasing use of 1,3-Dimethylurea as a nitrogen source in fertilizers and as a precursor in pharmaceutical synthesis. The presence of established chemical manufacturing facilities and a focus on agricultural productivity further support market expansion. Additionally, the region demonstrates a shift towards sustainable agricultural practices, which may influence the demand for specialty chemicals like 1,3-Dimethylurea.

In Europe, countries such as Germany, France, the UK, Italy, and Russia play critical roles in the market. The European chemical sector is highly regulated, prompting manufacturers to innovate in their production methods and applications of 1,3-Dimethylurea. Additionally, the increasing emphasis on sustainable practices and environmental compliance is likely to drive growth as industries look for compliant alternatives that can enhance soil health and crop yield. The European market also benefits from strong research and development activities that explore new applications of 1,3-Dimethylurea in various sectors, including pharmaceuticals and agrochemicals.

The Asia-Pacific region is witnessing rapid industrialization and urbanization, particularly in countries like China, Japan, South Korea, India, and Indonesia. China stands out as a significant market for 1,3-Dimethylurea due to its extensive agricultural sector and its need for chemical fertilizers. The growing middle class in these nations is contributing to increased consumer spending and agricultural productivity, which in turn enhances demand for nitrogen-rich fertilizers. Japan and South Korea are focusing more on high-value applications in pharmaceuticals and specialty chemicals, promoting further growth in this sector.

In Latin America, countries like Mexico, Brazil, Argentina, and Colombia are beginning to see an uptick in the demand for 1,3-Dimethylurea, primarily driven by agricultural needs. As the agriculture sector strives to improve crop yields and enhance sustainability, the use of chemical fertilizers is expected to rise. Brazil, in particular, is investing in agricultural technology, which could promote the use of specialty chemicals in enhancing productivity.

In the Middle East and Africa, especially in Turkey, Saudi Arabia, the UAE, and other regions, the market for 1,3-Dimethylurea is still emerging. The region&#;s growing population and the need to improve agricultural output are creating opportunities. However, this market may face challenges such as limited local production capabilities and regulations that could affect import and usage patterns.

Demographically, the increasing population and a growing focus on food security are pushing agricultural development across all regions, which directly influences the market for fertilizers including 1,3-Dimethylurea. Urbanization trends are also resulting in enhanced demand for efficient agricultural practices as cities expand, leading to a greater push for innovative solutions in farming. The rise of the middle class in Asia-Pacific and Latin America is contributing to increasing demands for food, thereby impacting fertilizer markets positively. Moreover, educational trends and awareness about sustainable agricultural practices are shaping consumer choices, which may further dictate market dynamics in the coming years.

Overall, while the market for 1,3-Dimethylurea varies significantly across regions, common themes of agricultural demand and sustainability are likely to drive growth globally.

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Future Trajectory: Growth Opportunities in the 1,3-Dimethylurea (CAS 96-31-1) Market

The 1,3-Dimethylurea market is projected to experience robust growth, driven by increasing applications in agrochemicals, pharmaceuticals, and chemical synthesis. Innovative growth drivers include the rising demand for high-performance fertilizers in agriculture and advancements in pharmaceuticals that utilize 1,3-Dimethylurea as an intermediate.

Market entry strategies should focus on establishing partnerships with agricultural companies and pharmaceutical manufacturers, alongside tapping into emerging markets where agricultural practices are evolving. Leveraging e-commerce platforms for direct sales can also enhance market penetration.

Potential market disruptions could arise from shifts towards sustainable practices, prompting the exploration of bio-based alternatives or stricter regulations on chemical usage.

The expected compound annual growth rate (CAGR) for the 1,3-Dimethylurea market during the forecast period is around 5-7%. The market size is anticipated to expand significantly, reflecting heightened industrial demand.

Consumer segments include agricultural producers, pharmaceutical companies, and chemical manufacturers. Factors influencing purchasing decisions encompass product quality, regulatory compliance, pricing competitiveness, and supplier reliability. Increasing awareness of the importance of sustainable agricultural practices may further influence purchasing trends, pushing operators towards innovative and environmentally friendly sourcing options.

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Water Soluble Cutting Oil

1,3-DIMETHYLUREA

1,3-Dimethylurea is utilized in the synthesis of various chemicals, including caffeine and theophylline, and is also a crucial component in the production of fiber treatment agents and herbicides.

The estimated global production of 1,3-Dimethylurea is less than 25,000 tons, with applications spanning from pharmaceutical manufacturing to the formulation of pH regulators and cleaning products.

1,3-Dimethylurea is soluble in water and alcohols, with a melting point of -3°C, and its physical properties make it suitable for use in a range of chemical reactions and formulations.

CAS number: 96-31-1

EC number: 202-498-7

Chemical Formula: CH&#;NHCONHCH&#;

Molar Mass: 88.11 g/mol

Synonyms: N,N&#;-Dimethylurea, DMU, 1,3-Dimethylurea, 1,3-DIMETHYLUREA, N,N'-Dimethylurea, 96-31-1, sym-Dimethylurea, Urea, N,N'-dimethyl-, Symmetric dimethylurea, Urea, 1,3-dimethyl-, N,N'-Dimethylharnstoff, 1,3-Dimethyl urea, NSC , BRN , AI3-, MFCD, WAM6DR9I4X, DMU, DTXSID, CHEBI:, Urea,3-dimethyl-, Urea,N'-dimethyl-, NSC-, 1,3-Dimethylurea, 98%, WLN: 1MVM1, CCRIS , HSDB , EINECS 202-498-7, UNII-WAM6DR9I4X, Dimethylharnstoff, 1.3-Dimethylurea, N,N-Dimethyl-Urea, 1,3 dimethyl urea, N,N'-dimethyl urea, 1,1'-Dimethylurea, 1,3-Dimethylcarbamide, bmse, EC 202-498-7, UREA,1,3-DIMETHYL, (CH3NH)2CO, DIMETHYL UREA [INCI], DIMETHYLUREA, N,N'-, N,N'-Dimethylurea, ~98%, DTXCID, CHEMBL, 1,3-DIMETHYLUREA [HSDB], NSC, NSC, Tox21_, 1,3-Dimethylurea;N,N'-Dimethylurea, NSC-, AKOS, CS-W, PB, CAS-96-31-1, NCGC-01, NCGC-01, SY, N,N inverted exclamation mark -Dimethylurea, A, D, FT-, EN300-, P, ethyl 5-oxo-2,3-diphenyl cyclopentanecarboxylate, A, N,N'-Dimethylurea, (sym.), >=99% (from N), Q, W-, N,N'-Dimethylurea, PESTANAL(R), analytical standard,

F-, N,N'-Dimethylurea, (sym.), >=95.0% (HPLC), technical, InChI=1/C3H8N2O/c1-4-3(6)5-2/h1-2H3,(H2,4,5,6), Urea, 1,3-dimethyl-, sym-Dimethylurea, N,N'-Dimethylurea, Symmetric dimethylurea, 1,3-Dimethylurea, (CH3NH)2CO, 1,1'-Dimethylurea, DMU, N,N' Dimethylharnstoff, NSC , (CH3NH)2CO, 1,1'-Dimethylurea, 1,3-dimethylurea, DMU, N,N'-Dimethylharnstoff, N,N'-dimethylurea, NSC , Symmetric dimethylurea, sym-Dimethylurea, urea, 1,3-dimethyl-,

syM,N,N'-DIMETHYLUREA, (CH3NH)2CO, AKOS B, 1.3-DiMethyl u, 1,3-dimethyl-ure, SYM-DIMETHYLUREA, 1,3-DIMETHYLUREA, n,n&#;-dimethyl-ure,Dimethylcarbamide

N,N'-Dimethyl urea, 1,3-Dimethylurea, N,N&#;-dimethyl-Urea, 1,3-dimethyl-ure, n,n&#;-dimethylharnstoff, n,n&#;-dimethylharnstoff (german), n,n&#;-dimethylurea, sym-dimethylurea, Urea, 1,3-dimethyl-, sym-Dimethylurea, N,N'-Dimethylurea, Symmetric dimethylurea, 1,3-Dimethylurea, (CH3NH)2CO, 1,1'-Dimethylurea, DMU, N,N'-Dimethylharnstoff, NSC , Urea, N,N&#;-dimethyl-, Urea, 1,3-dimethyl-, N,N&#;-Dimethylurea, 1,3-Dimethylurea, Symmetric dimethylurea, sym-Dimethylurea,

NSC , NSC , Urea,1,3-dimethyl- (8CI), N,N'-Dimethylurea, NSC , NSC , Symmetric dimethylurea, sym-Dimethylurea, Urea,N,N&#;-dimethyl, UNII-WAM6DR9I4X, MeNHNCONHMe, sym-Dimethylurea, N,N`-Dimethylurea,

1,3-Dimethylurea is an organic chemical substance, CAS No.:96-31-1, molecular formula: C3H8N2O

1,3-Dimethylurea is a colorless, volatile liquid with a penetrating odor.

1,3-Dimethylurea is a urea derivative and used as an intermediate in organic synthesis.

1,3-Dimethylurea is a colorless crystalline powder with little toxicity.

1,3-Dimethylurea is also used for synthesis of caffeine, pharmachemicals, textile aids, herbicides and other.

In the textile processing industry 1,3-Dimethylurea is used as intermediate for the production of formaldehyde-free easy-care finishing agents for textiles.

In the Swiss Product Register there are 38 products containing 1,3-Dimethylurea, among them 17 products intended for consumer use.

Product types are e.g. paints and cleaning agents.

The content of 1,3-Dimethylurea in consumer products is up to 10 %.

Use in cosmetics has been proposed, but there is no information available as to 1,3-Dimethylurea's actual use in such applications.

1,3-Dimethylurea is a white crystals.

1,3-Dimethylurea is a colorless, volatile liquid with a penetrating odor.

1,3-Dimethylurea is soluble in water and alcohols and has a melting point of -3°C.

1,3-Dimethylurea is a colorless powder, used as building block for active ingredients or intermediate for formaldehyde-free textile additives.

1,3-Dimethylurea is a member of the class of ureas that is urea substituted by methyl groups at positions 1 and 3.

1,3-Dimethylurea is water soluble.

1,3-Dimethylurea is an organic compound that has been shown to bind to the carbonyl group of proteins and act as a hydrogen-bond donor.

The nitrogen atoms are coordinated to form two pyramidal structures with the hydrogen bonding between the nitrogen atoms.

This coordination geometry leads to a molecule that is planar and the frequency shift of IR spectroscopy data confirms this structure.

The reaction mechanism for 1,3-Dimethylurea begins with an attack by the oxygen atom on the carbon atom of tetramethylurea forming an intermediate called trimethylamine, which then reacts with trifluoroacetic acid (TFA) leading to the formation of 1,3-Dimethylurea.

1,3-Dimethylurea is a colorless crystals.

1,3-Dimethylurea Market revolves around the production and distribution of the chemical compound 1,3-Dimethylurea, identified by the CAS (Chemical Abstracts Service) number 96&#;31&#;1.

1,3-Dimethylurea is a derivative of urea and is characterized by its molecular structure, consisting of two methyl groups attached to the nitrogen atoms of the urea molecule.

1,3-Dimethylurea Market plays a crucial role in the chemical industry, serving as a key intermediate in the synthesis of various chemicals, including pharmaceuticals and agrochemicals.

1,3-Dimethylurea is utilized as a building block in the creation of complex molecules, contributing to advancements in drug development and agricultural formulations.

The growth of the 1,3-Dimethylurea Market is propelled by several key factors.

Primarily, 1,3-Dimethylurea&#;s significance as an intermediate in the synthesis of pharmaceuticals drives its demand, as 1,3-Dimethylurea plays a crucial role in the development of diverse drug compounds.

Uses of 1,3-Dimethylurea:

1,3-Dimethylurea is used for synthesis of caffeine, pharmachemicals, textile aids, herbicides and other.

In the textile processing industry 1,3-Dimethylurea is used as intermediate for the production of formaldehyde-free easy-care finishing agents for textiles.

1,3-Dimethylurea is a colorless crystalline powder with little toxicity.

1,3-Dimethylurea is also used for synthesis of caffeine, pharmachemicals, textile aids, herbicides and other.

In the textile processing industry 1,3-Dimethylurea is used as intermediate for the production of formaldehyde-free easy-care finishing agents for textiles.

1,3-Dimethylurea is used in the following products: pH regulators and water treatment products and laboratory chemicals.

1,3-Dimethylurea is used in the following areas: health services and scientific research and development.

1,3-Dimethylurea is used for the manufacture of: chemicals.

1,3-Dimethylurea is a urea derivative and used as an intermediate in organic synthesis.

1,3-Dimethylurea is a colorless crystalline powder with little toxicity.

In medicine, 1,3-Dimethylurea is used to synthesize theophylline, caffeine and nifedipine hydrochloride, etc.

1,3-Dimethylurea is used by professional workers (widespread uses), in formulation or re-packing and at industrial sites.

1,3-Dimethylurea is used in the following products: pH regulators and water treatment products and laboratory chemicals.

1,3-Dimethylurea is used in the following areas: health services and scientific research and development.

Use in cosmetics of 1,3-Dimethylurea has been proposed, but there is no information available as to its actual use in such applications.

1,3-Dimethylurea is used for synthesis of caffeine, theophylline, pharmachemicals, textile aids, herbicides and others.

1,3-Dimethylurea is used in the textile processing industry.

1,3-Dimethylurea is also used for synthesis of caffeine, pharmachemicals, textile aids, herbicides and other.

1,3-Dimethylurea is used as an intermediate in organic synthesis. Ungraded products supplied by Spectrum are indicative of a grade suitable for general industrial use or research purposes and typically are not suitable for human consumption or therapeutic use.

1,3-Dimethylurea is used as an intermediate in the synthesis of theophylline and caffeine, and also used in the production of fiber treatment agents

1,3-Dimethylurea is used in manufacturing synthetic caffeine, resins and drugs.

1,3-Dimethylurea is used as a catalyst for condensation of methylamine with urea.

1,3-Dimethylurea is used as a pharmaceutical drug to treat hyperammonemia.

1,3-Dimethylurea is a urea derivative and used as an intermediate in organic synthesis.

1,3-Dimethylurea is used in pharmaceutical manufacturing.

1,3-Dimethylurea is used as an intermediate to make caffeine, pharmachemicals, textile aids, herbicides, paints, and cleaning products.

1,3-Dimethylurea is used as textile auxiliaries to produce formaldehyde-free anti-wrinkle finishing products.

1,3-Dimethylurea is used in cosmetics as an emollient.

1,3-Dimethylurea is used in medicine and can produce a variety of raw materials.

1,3-Dimethylurea is used in chemical industry, it can synthesize a variety of chemical products.

1,3-Dimethylurea is a urea derivative and used as an intermediate in organic synthesis.

1,3-Dimethylurea is used for synthesis of caffeine, theophylline, pharmachemicals, textile aids, herbicides and others.

1,3-Dimethylurea is used in the textile processing industry.

Pharmaceutical intermediates, 1,3-Dimethylurea is also used in the production of fiber treatment agents.

In the textile processing industry 1,3-Dimethylurea is used as intermediate for the production of formaldehyde-free easy-care finishing agents for textiles.

1,3-Dimethylurea is used for synthesis of caffeine, pharmachemicals, textile aids, herbicides and other.

In the textile processing industry 1,3-Dimethylurea is used as intermediate for the production of formaldehyde-free easy-care finishing agents for textiles.

1,3-Dimethylurea is used for synthesis of caffeine, theophylline, pharmachemicals, textile aids, herbicides and others.

In the textile processing industry 1,3-Dimethylurea is used as intermediate for the production of formaldehyde-free easy-care finishing agents for textiles.

The estimated world production of 1,3-Dimethylurea is estimated to be less than 25,000 tons.

Other release to the environment of 1,3-Dimethylurea is likely to occur from: indoor use (e.g. machine wash liquids/detergents, automotive care products, paints and coating or adhesives, fragrances and air fresheners).

Release to the environment of 1,3-Dimethylurea can occur from industrial use: formulation of mixtures.

Release to the environment of 1,3-Dimethylurea can occur from industrial use: as an intermediate step in further manufacturing of another substance (use of intermediates), in processing aids at industrial sites and as processing aid.

1,3-Dimethylurea is a urea derivative and used as an intermediate in organic synthesis.

In the Swiss Product Register there are 38 products containing 1,3-Dimethylurea, among them 17 products intended for consumer use.

Product types of 1,3-Dimethylurea are e.g. paints and cleaning agents.

The content of 1,3-Dimethylurea in consumer products is up to 10 %.

1,3-Dimethylurea can be used as a starting material to synthesize N,N&#;-dimethyl-6-amino uracil.

In combination with β-cyclodextrin derivatives, to form low melting mixtures (LMMs), which can be used as solvents for hydroformylation and Tsuji-Trost reactions.

To synthesize N,N&#;-disubstituted-4-aryl-3,4-dihydropyrimidinones via Biginelli condensation under solvent-free conditions.

Features of 1,3-Dimethylurea:

Good stability:

1,3-Dimethylurea has good stability and are suitable for various synthetic chemical reactions, ensuring the stability and reliability of our customers' production processes.

Analysis of 1,3-Dimethylurea:

Synthesis Analysis:

A practically simple, mild, and efficient method has been developed for the synthesis of N-substituted ureas by nucleophilic addition of amines to potassium isocyanate in water without an organic co-solvent.

Chemical Reactions Analysis:

The reaction of 1,3-Dimethylurea with formaldehyde has been studied in detail using quantitative on-line NMR spectroscopy.

The system undergoes only four reactions and, unlike urea&#;formaldehyde, does not form polymers.

Physical And Chemical Properties Analysis:

1,3-Dimethylurea is a colorless crystalline powder with little toxicity.

The effects of concentration variation of 1,3-DMU in distilled water on dielectric and electrical properties have been discussed to gain information about the self-aggregative nature of 1,3-Dimethylurea and dissociation process in aqueous solutions

Molecular Structure Analysis:

1,3-Dimethylurea forms needle-shaped crystals.

The Raman spectra of DMU crystal have been measured, and the density function theory with a B3LYP/6-311G basis set has been used to optimize the geometry structure and calculate the vibrational frequency of gas phase DMU.

Purification Methods of 1,3-Dimethylurea:

Crystallise the urea from acetone/diethyl ether by cooling in an ice bath.

Also crystallise 1,3-Dimethylurea from EtOH and dry it at 50o/5mm for 24hours.

Production Method of 1,3-Dimethylurea:

Industry uses molten urea and monomethyl amine action to make.

First, the area into the melting tank, heated to 130-135C to melt 1,3-Dimethylurea, transferred to the reaction tower has been heated to 110-120C, continue to raise the temperature to 150-175 &#;, began to pass the purified monomethyl amine gas, until the monomethyl amine all through, that is, the reaction is completed, the creation of even dimethyl urea finished products.

Handling And Storage of 1,3-Dimethylurea:

Precautions for safe handling:

Hygiene measures:

Handle in accordance with good industrial hygiene and safety practice.

Wash hands before breaks and at the end of workday.

Conditions for safe storage, including any incompatibilities:

Storage conditions:

Store in cool place.

Keep container tightly closed in a dry and well-ventilated place.

Storage class:

Storage class (TRGS 510): 13:

Non Combustible Solids

Stability And Reactivity of 1,3-Dimethylurea:

Reactivity:

1,3-Dimethylurea is an amide.

Amides/imides react with azo and diazo compounds to generate toxic gases.

Flammable gases are formed by the reaction of organic amides/imides with strong reducing agents.

Amides are very weak bases (weaker than water).

Imides are less basic yet and in fact react with strong bases to form salts.

That is, they can react as acids.

For more 1,3-dimethylurea Flake Manufacturerinformation, please contact us. We will provide professional answers.

Mixing amides with dehydrating agents such as P2O5 or SOCl2 generates the corresponding nitrile.

The combustion of these compounds generates mixed oxides of nitrogen (NOx).

Chemical stability:

Stable under recommended storage conditions.

Possibility of hazardous reactions:

No data available

Conditions to avoid:

No data available

First Aid Measures of 1,3-Dimethylurea:

General advice:

Consult a physician.

Show this material safety data sheet to the doctor in attendance.

If inhaled:

If breathed in, move person into fresh air.

Consult a physician.

In case of skin contact:

Wash off with soap and plenty of water.

Consult a physician.

In case of eye contact:

Flush eyes with water as a precaution.

If swallowed:

Never give anything by mouth to an unconscious person.

Rinse mouth with water.

Consult a physician.

Indication of any immediate medical attention and special treatment needed:

No data available

Fire Fighting Measures of 1,3-Dimethylurea:

Suitable extinguishing media:

Use water spray, alcohol-resistant foam, dry chemical or carbon dioxide.

Further information:

No data available

Accidental Release Measures of 1,3-Dimethylurea:

Environmental precautions:

Do not let product enter drains.

Methods and materials for containment and cleaning up:

Pick up and arrange disposal without creating dust.

Sweep up and shovel.

Keep in suitable, closed containers for disposal.

Exposure Controls/Personal Protection of 1,3-Dimethylurea:

Personal protective equipment:

Eye/face protection:

Use equipment for eye protection.

Skin protection:

Handle with gloves.

Wash and dry hands.

Full contact:

Material: Nitrile rubber

Minimum layer thickness: 0,11 mm

Break through time: 480 min

Splash contact:

Material: Nitrile rubber

Minimum layer thickness: 0,11 mm

Break through time: 480 min

Body Protection:

Choose body protection

Respiratory protection:

Respiratory protection is not required.

Control of environmental exposure:

Do not let product enter drains.

Identifiers of 1,3-Dimethylurea:

CAS No.: 96-31-1

Molecular Formula: C3H8N2O

InChIKeys: InChIKey=MGJKQDOBUOMPEZ-UHFFFAOYSA-N

Molecular Weight: 88.11

Exact Mass: 88.11

EC Number: 202-498-7

UNII: WAM6DR9I4X

ICSC Number:

NSC Number: |

DSSTox ID: DTXSID

Color/Form: RHOMBIC BIPYRAMIDAL CRYSTALS FROM CHLOROFORM-ETHER|COLORLESS PRISMS

HScode:

PSA: 41.1

XLogP3: -0.5

Appearance: N,n'-dimethylurea appears as colorless crystals. (NTP, )

Density: 1.142 g/cm3

Freezing point: 103'C Min

Volatile Content: &#; 0.2%

Melting point: 104'C

CAS number: 96-31-1

EC number: 202-498-7

Hill Formula: C&#;H&#;N&#;O

Chemical formula: CH&#;NHCONHCH&#;

Molar Mass: 88.11 g/mol

HS Code: 19 00

Boiling point: 268 - 270 °C ( hPa)

Density: 1.14 g/cm3 (20 °C)

Flash point: 157 °C DIN

Ignition temperature: 400 °C

Melting Point: 101 - 104 °C

pH value: 9.0 - 9.5 (H&#;O)

Vapor pressure: Bulk density: 500 kg/m3

Solubility: 765 g/l

Chemical Name: N,N&#;-dimethylurea

CAS No.: 96-31-1

Molecular Formula: C3H8N2O

Molecular Weight: 88.

PSA: 41.

LogP: 0.

Appearance & Physical State: white flake

Density: 1.142

Boiling Point: 268-270ºC

Melting Point: 101-105ºC

Flash Point: 157ºC

Refractive Index: 1.413

Water Solubility: 765 g/L (21.5 ºC)

Stability: Stable under normal temperatures and pressures.

Storage Condition: Store at RT.

Melting point: 101-104 °C(lit.)

Boiling point: 268-270 °C(lit.)

Density: 1.142

Properties of 1,3-Dimethylurea:

Chemical formula: C3H8N2O

Molar mass: 88.110 g·mol&#;1

Appearance: Colorless, waxy crystals

Odor: Odorless

Density: 1.142 g mL&#;1

Melting point: 104.4 °C; 219.8 °F; 377.5 K

Boiling point: 269.1 °C; 516.3 °F; 542.2 K

Solubility in water: 765 g L&#;1

Molecular Weight: 88.11 g/mol

XLogP3: -0.5

Hydrogen Bond Donor Count: 2

Hydrogen Bond Acceptor Count: 1

Rotatable Bond Count: 0

Exact Mass: 88. g/mol

Monoisotopic Mass: 88. g/mol

Topological Polar Surface Area: 41.1&#;²

Heavy Atom Count: 6

Complexity: 46.8

Isotope Atom Count: 0

Defined Atom Stereocenter Count: 0

Undefined Atom Stereocenter Count: 0

Defined Bond Stereocenter Count: 0

Undefined Bond Stereocenter Count: 0

Covalently-Bonded Unit Count: 1

Compound Is Canonicalized: Yes

Physical state: flakes

Color: colorless

Odor: amine-like

Melting point/freezing point:

Melting point/range: 103 - 106 °C

Initial boiling point and boiling range: 268 - 270 °C - lit.

Flammability (solid, gas): No data available

Upper/lower flammability or explosive limits: No data available

Flash point: 157 °C - closed cup

Autoignition temperature: No data available

Decomposition temperature: No data available

pH: 9,0 - 9,5

Viscosity

Viscosity, kinematic: No data available

Viscosity, dynamic: No data available

Water solubility: 765 g/l at 21,5 °C - soluble

Partition coefficient:

n-octanol/water: log Pow: -0,783

Vapor pressure: No data available

Density: 1,14 g/cm3 at 20 °C

Relative density: No data available

Relative vapor density: No data available

Particle characteristics: No data available

Explosive properties: No data available

Oxidizing properties: No data available

Other safety information:

Bulk density 0,50 g/l

Molecular Formula: CH3NHCONHCH3

CAS No: 96-31-1

EINECS: 202-498-7

Molecular Weight: 88.11

Appearance: White Crystals

Assay: &#; 95%

Assay: &#;97.5%

Water: &#;0.5

Density: 0.9±0.1 g/cm3

Boiling Point: 269.0±0.0 °C at 760 mmHg

Melting Point: 101-104 °C(lit.)

Molecular Formula: C3H8N2O

Molecular Weight: 88.108

Flash Point: 124.3±18.9 °C

Exact Mass: 88.

PSA: 41.

LogP: -1.01

Vapour Pressure: 0.0±0.5 mmHg at 25°C

Index of Refraction: 1.414

Storage condition: Store at RT.

Water Solubility: 765 g/L (21.5 ºC)

Synonyms: 1,3-Dimethylurea

Molecular Weight: 88.11

Molecular Formula: C3H8N2O

Thermochemistry of 1,3-Dimethylurea:

Std enthalpy of formation (ΔfH&#;298): &#;312.1&#;&#;312.1 kJ mol&#;1

Std enthalpy of combustion (ΔcH&#;298): &#;2.&#;&#;2. MJ mol&#;1

Magnetic susceptibility (χ): -55.1·10&#;6 cm3/mol

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