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N,N-Di-hiodrocsaileitiléiamín (Uimh. CAS: 7087-68-5)

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Táirgí Réadmhaoin

N,N-Diisopropylethylamine (CAS NO.: 7087-68-5) - Honor Pigments
N,N-Di-hiodrocsaileitiléiamín (Uimh. CAS: 7087-68-5)

CAS NO.: 7087-68-5

Ábhar:99.00%

Application: Used as a non-nucleophilic base in reactions such as peptide coupling, alkylation, enolboration, and Pd(0)-catalyzed alkoxycarbonylation; acts as a proton scavenger and activator for chiral catalysts. etc.

Déan teagmháil linn

Cur síos

Forbhreathnú ar an Táirge

N,N-Diisopropylethylamine (also known as DIPEA, N-Ethyldiisopropylamine, or Ethyldiisopropylamine) CAS No.: 7087-68-5 , with the chemical formula C₈H₁₉N and a molecular weight of 129.24 g/mol. It is a colorless liquid with an amine-like odor. This compound belongs to the class of tertiary amines and is primarily used as a non-nucleophilic base in organic synthesis, though it is subject to safety regulations due to its flammable, corrosive, and irritant properties.

Airíonna

N,N-Diisopropylethylamine exhibits the following key physical and chemical properties:

  • Stádas fisiceach: Leachtach (ag teocht an tseomra).
  • Cuma: Colorless to pale yellow liquid.
  • Boladh: Amine-like.
  • Pointe leá: -50 to -46 °C.
  • An t-eadhon fiuchta: 126-127 °C.
  • Dlús: 0.742 g/mL (at 25 °C).
  • Intuaslagthacht: Slightly soluble in water (4.01 g/L at 20 °C); miscible with organic solvents like ethanol and ether.
  • Cobhsaíocht: Stable under normal conditions; incompatible with strong acids, oxidizing agents, and acid chlorides; hygroscopic.
  • Tocsaineacht: Moderately toxic; acute toxicity by inhalation (Category 3) and oral (Category 4); causes severe eye damage (Category 1), skin and respiratory irritation; target organ is the respiratory system.

Iarratais

The primary applications of N,N-Diisopropylethylamine include:

  • Idirmheánach na Síntéise Orgánaí: Used as a non-nucleophilic base in reactions such as peptide coupling, alkylation, enolboration, and Pd(0)-catalyzed alkoxycarbonylation; acts as a proton scavenger and activator for chiral catalysts.
  • Reagent: Employed in the synthesis of pharmaceuticals (e.g., mannosylated ovalbumin peptides), marine toxins like Gambierol, indenopyrones, and vinyl sulfones; investigated in lipase-catalyzed syntheses and hydrogenation processes.
  • Eile: Serves as a catalyst and base in various organic reactions, including substitution reactions and the preparation of fine chemicals.

Aicmiú

The following table outlines the classification of N,N-Diisopropylethylamine based on chemical properties, uses, and regulations:

Cineál Aicmithe Catagóir Shonrach Cur síos
Rang Ceimice Tertiary Amine A sterically hindered amine, non-nucleophilic and used as a base in organic chemistry.
Aicme Úsáide Organic Synthesis Reagent/Base Primarily a non-nucleophilic base and reagent in laboratory and industrial synthesis.
Aicme Guaise Flammable Liquid (UN 1993); Corrosive; Toxic Flammable (Category 2, flash point 9.5 °C); acute toxic (inhalation Category 3, oral Category 4); eye damage (Category 1); irritant (skin, respiratory); aquatic chronic (Category 2).
Aicme Rialála Controlled Chemical (REACH, TSCA, CLP) Listed under EU REACH, US TSCA, and CLP regulations; WGK 2 in Germany; subject to environmental release controls and hazardous substance handling.

Why Choose Honor Pigments?

  • 🌍 Global Export Expertise — Trusted by customers in 40+ countries for consistent quality and reliable supply
  • ✅ Strict Quality Control — ISO 9001 certified with batch-to-batch consistency and zero-defect policy
  • 💰 OEM Production Advantage — Competitive pricing without compromising pigment performance
  • 🧪 Technical Support — Free color matching, formulation advice and sample testing before bulk order

📩 Need more details?

Request TDS, SDS, or a free sample for testing.

Táirgí gaolmhara

Forbhreathnú ar an Táirge

N,N-Diisopropylethylamine (also known as DIPEA, N-Ethyldiisopropylamine, or Ethyldiisopropylamine) CAS No.: 7087-68-5 , with the chemical formula C₈H₁₉N and a molecular weight of 129.24 g/mol. It is a colorless liquid with an amine-like odor. This compound belongs to the class of tertiary amines and is primarily used as a non-nucleophilic base in organic synthesis, though it is subject to safety regulations due to its flammable, corrosive, and irritant properties.

Airíonna

N,N-Diisopropylethylamine exhibits the following key physical and chemical properties:

  • Stádas fisiceach: Leachtach (ag teocht an tseomra).
  • Cuma: Colorless to pale yellow liquid.
  • Boladh: Amine-like.
  • Pointe leá: -50 to -46 °C.
  • An t-eadhon fiuchta: 126-127 °C.
  • Dlús: 0.742 g/mL (at 25 °C).
  • Intuaslagthacht: Slightly soluble in water (4.01 g/L at 20 °C); miscible with organic solvents like ethanol and ether.
  • Cobhsaíocht: Stable under normal conditions; incompatible with strong acids, oxidizing agents, and acid chlorides; hygroscopic.
  • Tocsaineacht: Moderately toxic; acute toxicity by inhalation (Category 3) and oral (Category 4); causes severe eye damage (Category 1), skin and respiratory irritation; target organ is the respiratory system.

Iarratais

The primary applications of N,N-Diisopropylethylamine include:

  • Idirmheánach na Síntéise Orgánaí: Used as a non-nucleophilic base in reactions such as peptide coupling, alkylation, enolboration, and Pd(0)-catalyzed alkoxycarbonylation; acts as a proton scavenger and activator for chiral catalysts.
  • Reagent: Employed in the synthesis of pharmaceuticals (e.g., mannosylated ovalbumin peptides), marine toxins like Gambierol, indenopyrones, and vinyl sulfones; investigated in lipase-catalyzed syntheses and hydrogenation processes.
  • Eile: Serves as a catalyst and base in various organic reactions, including substitution reactions and the preparation of fine chemicals.

Aicmiú

The following table outlines the classification of N,N-Diisopropylethylamine based on chemical properties, uses, and regulations:

Cineál Aicmithe Catagóir Shonrach Cur síos
Rang Ceimice Tertiary Amine A sterically hindered amine, non-nucleophilic and used as a base in organic chemistry.
Aicme Úsáide Organic Synthesis Reagent/Base Primarily a non-nucleophilic base and reagent in laboratory and industrial synthesis.
Aicme Guaise Flammable Liquid (UN 1993); Corrosive; Toxic Flammable (Category 2, flash point 9.5 °C); acute toxic (inhalation Category 3, oral Category 4); eye damage (Category 1); irritant (skin, respiratory); aquatic chronic (Category 2).
Aicme Rialála Controlled Chemical (REACH, TSCA, CLP) Listed under EU REACH, US TSCA, and CLP regulations; WGK 2 in Germany; subject to environmental release controls and hazardous substance handling.

Why Choose Honor Pigments?

  • 🌍 Global Export Expertise — Trusted by customers in 40+ countries for consistent quality and reliable supply
  • ✅ Strict Quality Control — ISO 9001 certified with batch-to-batch consistency and zero-defect policy
  • 💰 OEM Production Advantage — Competitive pricing without compromising pigment performance
  • 🧪 Technical Support — Free color matching, formulation advice and sample testing before bulk order

📩 Need more details?

Request TDS, SDS, or a free sample for testing.

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