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4-(Dipropylamino)-3,5-dinitrobenzenesulfonamide

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Identification
Molecular formula
C12H18N4O6S
CAS number
20136-76-5
IUPAC name
4-(dipropylamino)-3,5-dinitro-benzenesulfonamide
State
State

At room temperature, 4-(dipropylamino)-3,5-dinitrobenzenesulfonamide is typically a solid. It is not readily volatile and remains stable under ambient conditions.

Melting point (Celsius)
145.00
Melting point (Kelvin)
418.15
Boiling point (Celsius)
320.00
Boiling point (Kelvin)
593.15
General information
Molecular weight
360.35g/mol
Molar mass
360.3470g/mol
Density
1.4500g/cm3
Appearence

The compound typically appears as a yellow to orange crystalline solid. It may vary in hue depending on the exact sample and purity, but it generally maintains its bright coloration indicative of the nitro groups present in its structure.

Comment on solubility

Solubility of 4-(Dipropylamino)-3,5-dinitro-benzenesulfonamide

The solubility of 4-(dipropylamino)-3,5-dinitro-benzenesulfonamide is an intriguing topic due to its unique structure and functional groups. As a sulfonamide derivative, it possesses both hydrophobic and hydrophilic characteristics, leading to a nuanced solubility profile.

Factors Influencing Solubility

Several factors affect the solubility of this compound:

  • Polar and Non-Polar Interactions: The presence of the sulfonamide group introduces polar characteristics, while the dipropylamino moiety adds hydrophobic properties.
  • Temperature: Typically, an increase in temperature enhances solubility for many compounds, but specific behaviors can vary.
  • Solvent Type: The compound is likely to exhibit better solubility in organic solvents (such as ethanol or DMSO) compared to water due to its bulky hydrophobic tails.

Predicted Solubility Behavior

Due to its complex structure:

  • It may show limited solubility in polar solvents like water.
  • In contrast, expect a higher solubility in less polar organic solvents.

This solubility behavior highlights the intricate balance between hydrophilic and hydrophobic regions within the molecule, making it a fascinating subject of study for chemists interested in drug design and formulation. Understanding these solubility characteristics is crucial for predicting bioavailability and efficacy in pharmaceutical applications.

Interesting facts

Interesting Facts about 4-(Dipropylamino)-3,5-dinitro-benzenesulfonamide

4-(Dipropylamino)-3,5-dinitro-benzenesulfonamide, often referred to in scientific literature by its simpler name, is a compound that reflects the fascinating interplay of both organic and inorganic chemistry. Here are some intriguing aspects that highlight its significance:

  • Pharmaceutical Relevance: This compound belongs to a class of sulfonamides that have demonstrated biological activity, making them vital in medicinal chemistry. Sulfonamides have paved the way for numerous anti-bacterial drugs, showcasing their importance in the development of modern antibiotics.
  • Structural Diversity: The presence of multiple nitro groups on the aromatic ring significantly impacts the compound's reactivity and properties. Nitro-substituted aromatic compounds are particularly valuable in synthesizing dyes and explosives, highlighting their utility in various industries.
  • Versatility: The dipropylamino group enhances the lipophilicity of the compound, potentially increasing its bioavailability. This characteristic is crucial in drug development, where the absorption and distribution of compounds in biological systems can dictate overall efficacy.
  • Environmental Considerations: As with many chemical compounds, understanding the environmental impact and degradation pathways of 4-(dipropylamino)-3,5-dinitro-benzenesulfonamide is vital. Its potential toxicity to aquatic life and other organisms must be evaluated to ensure safe handling and use.
  • Research Opportunities: The combination of its structural features makes this compound a candidate for further research in areas such as reactive intermediates in organic synthesis, as well as potential applications in developing selective reagents in biochemical assays.

In summary, 4-(Dipropylamino)-3,5-dinitro-benzenesulfonamide exemplifies the importance of understanding complex organic compounds in both practical applications and theoretical studies. Its various functional groups offer a plethora of research opportunities and underscore the nuanced relationship between chemical structure and biological activity.

Synonyms
ORYZALIN
19044-88-3
Surflan
4-(Dipropylamino)-3,5-dinitrobenzenesulfonamide
Dirimal
Dirimal Extra
Compound 67019
EL 119
Dinitrodipropylsulfanilamide
3,5-Dinitro-N4,N4-dipropylsulfanilamide
3,5-Dinitro-N4,N4-dipropylsulphanilamide
EL-119
EPA Pesticide Chemical Code 104201
DTXSID8024238
CHEBI:73163
3,5-Dinitro-N(sup 4),N(sup 4)-dipropylsulfanilamide
662E385DWH
DTXCID904238
4-(dipropylamino)-3,5-dinitrobenzene-1-sulfonamide
3,5-dinitro-N,N-di(n-propyl)sulfanilamide
242-777-0
Benzenesulfonamide, 4-(dipropylamino)-3,5-dinitro-
Ryzelan
Rycelan
Rycelon
N4,N4-Dipropyl-3,5-dinitrosulfanilamide
NCGC00163815-04
4-(dipropylamino)-3,5-dinitro-benzenesulfonamide
Caswell No. 623A
C12H18N4O6S
Oryzalin [ANSI:BSI:ISO]
Oryzalin [ISO]
HSDB 6858
EINECS 242-777-0
BRN 2177305
Rizelan
UNII-662E385DWH
Oryzalin, 1
Oryzalin (Standard)
ORYZALIN [HSDB]
ORYZALIN [MI]
SCHEMBL55377
Oryzalin, analytical standard
CHEMBL295960
BDBM81743
Sulfanilamide, 3,5-dinitro-N(sup 4),N(sup 4)-dipropyl-
EL119
Tox21_400078
MFCD00078725
NSC648479
AKOS015888415
HY-147092R
NSC 648479
NSC-648479
NCGC00163815-01
NCGC00163815-02
NCGC00163815-03
NCGC00163815-05
AC-37590
AS-76251
DA-66376
FO166070
NCI60_016826
CAS-19044-88-3
HY-147092
NS00000515
Oryzalin, PESTANAL(R), analytical standard
4-Dipropylamino-3,5-dinitrobenzenesulfonamide
Sulfanilamide, 3,5-dinitro-N4,N4-dipropyl-
3,5-dinitro-N(4),N(4)-dipropylsulfanilamide
C18877
Q410996
4-(Dipropylamino)-3,5-dinitrobenzenesulfonimidic acid #