1,3-Diphenylurea | Solubility of Things

Identification

Molecular formula

C₁₃H₁₂N₂O

CAS number

102-07-8

IUPAC name

1,3-diphenylurea

State

1,3-Diphenylurea is typically in a solid state at room temperature.

Melting point (Celsius)

238.00

Melting point (Kelvin)

511.15

Boiling point (Celsius)

465.70

Boiling point (Kelvin)

738.85

General information

Molecular weight

212.25g/mol

Molar mass

212.2480g/mol

Density

1.3200g/cm³

Appearence

1,3-Diphenylurea appears as a white to off-white crystalline solid.

Comment on solubility

Solubility of 1,3-Diphenylurea

1,3-Diphenylurea (C₁₃H₁₂N₂O) is a compound whose solubility can be quite intriguing. It is known to be:

Moderately soluble in organic solvents such as ethanol and methanol.
Less soluble in water, which often poses challenges for applications that require aqueous solutions.

As a urea derivative, its solubility is influenced by various factors including:

**Polarity of the solvent**: The predominantly non-polar nature of 1,3-diphenylurea limits its solubility in polar solvents like water.
**Temperature**: Increased temperatures can enhance solubility in non-polar solvents, while lower temperatures may slow dissolution rates.
**Molecular structure**: The bulky phenyl groups contribute to hydrophobic interactions, further reducing solubility in polar environments.

In conclusion, while 1,3-diphenylurea shows some degree of solubility in organic solvents, its limited solubility in water makes it less favorable for certain chemical processes. This characteristic often necessitates the use of appropriate solvents to create effective solutions.

Interesting facts

Exploring 1,3-Diphenylurea

1,3-Diphenylurea is a fascinating compound that has captured the interest of scientists and researchers alike due to its versatile applications and intriguing chemical properties. Here are some interesting facts about this compound:

Structure and Formation: 1,3-Diphenylurea is a member of the urea family, which is characterized by the presence of the functional group -CONH₂. Its unique diphenyl structure allows for various interactions in chemical reactions.
Biological Relevance: This compound has shown potential in medicinal chemistry. It has been explored for its anti-tumor properties and might play a role in the development of new pharmaceutical agents.
Polymeric Applications: 1,3-Diphenylurea can act as a precursor for the synthesis of polyurethanes, which are commonly used in everyday materials such as foams, elastomers, and coatings.
Research Opportunities: The compound serves as a valuable subject for investigating the properties of urea derivatives in various fields, including materials science and organic chemistry.
Environmental Impact: As urea and its derivatives are often involved in nitrogen cycling, understanding their behavior in the environment is crucial. 1,3-Diphenylurea can help in studying nitrogenous waste and its management.

According to a renowned chemist, “The field of urea derivatives is not just about understanding their individual behavior, but about their potential in solving real-world problems.” The study of 1,3-diphenylurea exemplifies this sentiment as it bridges the gap between fundamental research and practical applications.

In summary, 1,3-diphenylurea is more than just a chemical formula; it is a window into the broader implications of urea chemistry and its essential role in various scientific domains.

Synonyms

1,3-Diphenylurea

102-07-8

N,N'-Diphenylurea

CARBANILIDE

Diphenylurea

Urea, N,N'-diphenyl-

Diphenylcarbamide

s-Diphenylurea

sym-Diphenylurea

Acardite

Acardite I

N-Phenyl-N'-phenylurea

1,3-Diphenylcarbamide

Karbanilid

N,N'-Difenylmocovina

USAF EK-534

Urea, 1,3-diphenyl-

Karbanilid [Czech]

1,3-diphenyl-urea

AD 30

Diphenylurea, 1,3-

N,N'-Difenylmocovina [Czech]

CCRIS 4634

NSC 227401

HSDB 2757

EINECS 203-003-7

94YD8RMX5B

BRN 0782650

DTXSID2025183

CHEBI:41320

AI3-52320

Urea-based compound, 7

CARBANILIDE [MI]

MFCD00003017

CARBANILIDE [HSDB]

NSC-227401

DTXCID305183

4-12-00-00741 (Beilstein Handbook Reference)

Urea,3-diphenyl-

Urea,N'-diphenyl-

WLN: RMVMR

1,3-Diphenylurea|Carbanalide

SR-01000398115

UNII-94YD8RMX5B

sDiphenylurea

symDiphenylurea

bis-phenyl-urea

3-diphenylurea

n,n'diphenylurea

1,3Diphenylurea

Zeonet U

2zjf

NPhenylN'phenylurea

n,n'-diphenyl-urea

N,N'Difenylmocovina

N, N'-diphenylurea

N,N'-diphenyl urea

1, 3-Diphenylurea

1,3Diphenylcarbamide

Urea, 1,3diphenyl

Urea, N,N'diphenyl

Kinome_598

Kinome_627

N,N'-bis-Phenylurea

Spectrum_000422

SpecPlus_000406

Spectrum2_001838

Spectrum3_001328

Spectrum4_001561

Spectrum5_000182

1,3-Diphenylurea, 98%

Oprea1_527136

BSPBio_003055

CBDivE_002165

KBioGR_002082

KBioSS_000902

SPECTRUM211126

MLS002207104

DivK1c_006502

SCHEMBL133103

SPBio_001915

CHEMBL354676

SCHEMBL21313806

BDBM25725

KBio1_001446

KBio2_000902

KBio2_003470

KBio2_006038

KBio3_002275

NSC8485

3e85

DTXCID601520407

DTXSID201036197

NSC-8485

RKL10128

Tox21_200068

CCG-38465

GEO-04213

ICCB1_000093

NSC227401

NSC794585

STK328350

AKOS000312994

CS-W015002

DB07496

FS-4202

HY-W014286

NSC-794585

SDCCGMLS-0066513.P001

NCGC00091344-01

NCGC00091344-02

NCGC00091344-03

NCGC00091344-04

NCGC00091344-05

NCGC00257622-01

AC-12855

CAS-102-07-8

SMR000112141

Carbanalide 100 microg/mL in Acetonitrile

EU-0067898

NS00010552

F20340

1,3-Diphenylurea, Vetec(TM) reagent grade, 98%

AQ-917/40171059

SR-01000398115-1

SR-01000398115-2

BRD-K13027645-001-02-0

Q27096716

203-003-7