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AgrochemicalsBromacil Impurity 1

SKU: SAB-08-A

Original price was: ₹60,000.00.Current price is: ₹50,000.00.

Bromacil Impurity 1

Name:1,3-Diisopropylurea

CAT. NO.:SAB-08-A

CAS NO.:4128-37-4

  • Description
  • Datasheet
  • Additional information

Description

Bromacil Impurity 1

Chemical Name 1,3-Diisopropylurea
Catalog Number SAB-08-A
Parent AI Bromacil
Synonyms Diptocarpamidine; N,N’-Bis(1-methylethyl)urea; N,N’-Diisopropylurea; NSC 112719
CAS Number 4128-37-4
Molecular Formula C₇H₁₆N₂O
Molecular Weight 144.21
Appearance White to Pale Yellow Solid
Melting Point 190-192°C
Shipping & Storage Information

 

Storage 20°C

Shipping: Free Shipping at Room Temperature in INDIA,  may vary elsewhere

Stability: Datasheet

Solubility DMSO (Slightly), Ethanol (Slightly), Methanol (Slightly)
Stability Stable under recommended storage conditions
Category Standards; Pharmaceutical/API Drug Impurities/Metabolites
Description &Applications 1,3-Diisopropylurea (1,3-DiU) is an organic compound that is widely used in scientific research and laboratory experiments. 1,3-DiU is an important reagent in organic synthesis and has many applications in biochemical, physiological and pharmacological research
References Singh, H.K. et al.: Photochem. Photobiol. Sci., 2, 151 (2003)

1,3-diisopropylurea (DIU), a fascinating molecule that has found its way into various scientific and industrial domains. With its unique structure and diverse reactivity, DIU has become an essential building block and reagent in the synthesis of numerous compounds. Let’s delve into the world of 1,3-diisopropylurea and explore its significance, properties, and applications.

Structural Insight:

1,3-Diisopropylurea is a chemical compound with the molecular formula C8H18N2O. Structurally, it features two isopropyl (CH3CHCH3) groups attached to a central urea core (NH2CONH2). This arrangement gives DIU its distinct characteristics, making it an intriguing compound to chemists.

Properties and Reactivity:

1,3-Diisopropylurea possesses several notable properties that contribute to its versatile reactivity:

  1. Steric Hindrance: The presence of bulky isopropyl groups imparts steric hindrance around the nitrogen atoms of the urea moiety. This feature influences the compound’s reactivity and selectivity in various reactions.
  2. Solubility: DIU exhibits good solubility in common organic solvents, making it readily available for use in various chemical reactions.
  3. Acid-Base Properties: Like urea, 1,3-diisopropylurea can act as a weak base, capable of forming hydrogen bonds with proton-donating species.

Applications:

The versatility of 1,3-diisopropylurea has led to its application in diverse fields of chemistry:

  1. Catalysis: DIU is often employed as a ligand or co-catalyst in transition metal-catalyzed reactions. Its steric hindrance and coordination properties make it a valuable tool for enhancing the selectivity and efficiency of catalytic processes.
  2. Peptide Synthesis: In the realm of organic synthesis, DIU finds use in peptide coupling reactions. It aids in the activation of carboxylic acids, facilitating the formation of amide bonds in the assembly of peptides and other amide-containing compounds.
  3. Polymer Chemistry: The reactivity of DIU has also found applications in polymer chemistry, particularly in the synthesis of functional polymers with tailored properties.
  4. Medicinal Chemistry: Some research suggests that DIU could potentially be used as a reagent in the synthesis of biologically active compounds, including pharmaceuticals.
  5. Material Science: The unique properties of 1,3-diisopropylurea have led to its exploration in the development of novel materials with specific electronic or optical properties.

Future Prospects:

As chemistry continues to advance, the applications of 1,3-diisopropylurea are likely to expand further. Researchers are constantly discovering new ways to harness its reactivity and properties, leading to innovative advancements in various scientific and industrial fields.

Additional information

Pack Size

50mg

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