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N N Di Isopropylethylamine

Price 640 INR/ Kilograms

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MOQ : 500 Kilograms

N N Di Isopropylethylamine Specification

Boiling point
127128C

Assay
>= 99.0%

EINECS No
230-934-9

Residue on Ignition
0.01%

Particle Size
Not applicable (liquid form)

Storage
Store in tightly closed container, cool and dry place

Viscosity
0.77 cP at 25C

Place of Origin
India

Loss on Drying
0.2%

Heavy Metal (%)
0.001%

Molecular Weight
129.24 g/mol

HS Code
29211990

Acid Value
<0.1 mg KOH/g

Melting Point
-50C

Moisture (%)
0.2%

Molecular Formula
C8H19N

Other Names
Hnigs base, DIPEA, N,N-Diisopropylethylamine

CAS No
7087-68-5

Type
Organic Base

Grade
Analytical, Industrial

Usage
Pharmaceutical Intermediates, Synthesis, Laboratory Reagent

Purity
99%

Appearance
Clear liquid

Application
Organic Synthesis, Pharmaceuticals, Peptide Coupling

Raw Material
Isopropylamine, Ethyl Bromide

Smell
Amine-like

Color
Colorless to pale yellow

Form
Liquid

Refractive Index
n20/D 1.387

Shelf Life
24 months

Stability
Stable under recommended handling and storage conditions

Flash Point
13C (closed cup)

Density
0.742 g/cm at 20C

Solubility
Miscible with most organic solvents

Impurities
0.05%

Peroxides
Absent

Transportation
UN 2734, Class 3, Packing Group II

About N N Di Isopropylethylamine

Boiling Point: 127 degree
Flammability: It is a flammable liquid.
0.742 g/mL0.742 g/mL
0.742g/mL at

25C25 C
25C
N,N-Diisopropylethylamine (DIPEA) is a colorless liquid with specifications including a minimum purity of 99%

Exceptional Purity and Quality

This N,N-Diisopropylethylamine features a purity of 99%, ensuring reliable results for demanding applications such as organic and pharmaceutical synthesis. Controlled impurity levels and low residue on ignition guarantee minimal side reactions and enhanced efficiency in your reactions.

Versatile Applications in Synthesis

DIPEA serves as an outstanding organic base and is essential in peptide coupling, pharmaceutical intermediate preparation, and laboratory experiments. Its miscibility with most organic solvents and amine-like scent make it a preferred choice in synthetic laboratories.

Safe Storage and Handling

Maintain the integrity and longevity of DIPEA by storing it in tightly closed containers in a cool, dry environment. With a shelf life of 24 months and proven stability under recommended conditions, it continues to perform optimally for extended periods.

FAQ's of N N Di Isopropylethylamine:

Q: How should N,N-Diisopropylethylamine be stored to maximize its shelf life?

A: Store DIPEA in a tightly closed container kept in a cool, dry place. Proper storage under these conditions ensures its stability and preserves its shelf life for up to 24 months.

Q: What applications does DIPEA serve in organic synthesis and pharmaceuticals?

A: DIPEA is extensively used as an organic base in peptide coupling reactions, pharmaceutical intermediate synthesis, and general laboratory research due to its high purity and miscibility with organic solvents.

Q: When is it appropriate to use N,N-Diisopropylethylamine in synthesis processes?

A: DIPEA is ideal for use during organic reactions requiring a strong, non-nucleophilic base-particularly in steps such as peptide coupling or amide bond formation to enhance yields and minimize by-products.

Q: Where is N,N-Diisopropylethylamine commonly manufactured and supplied from?

A: This compound is commonly manufactured, supplied, and traded in India, supporting both domestic and international chemical industries with reliable quality standards.

Q: What is the recommended process for handling and transporting DIPEA?

A: Handle DIPEA in well-ventilated areas, avoid sources of ignition due to its 13C flash point, and follow transportation regulations under UN 2734, Class 3, Packing Group II for safe and compliant shipping.

Q: How does using DIPEA benefit organic and pharmaceutical synthesis?

A: DIPEA offers high purity, controlled impurity levels, and excellent solvent compatibility, supporting efficient chemical reactions and reproducible results in pharmaceuticals and organic compound synthesis.

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