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2,2'-(Isopropylimino)diethanol, commonly referred to as IPDA, is a chemical compound characterized by its molecular formula C8H19NO2. It is a viscous, colorless liquid known for its strong chelating properties, which enable it to form stable complexes with metal ions. This makes IPDA a versatile compound for various industrial applications. Additionally, it is recognized for its low toxicity and is not classified as hazardous, which broadens its suitability for use in different sectors, including pharmaceuticals.

121-93-7

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121-93-7 Usage

Uses

Used in Corrosion Inhibition:
2,2'-(Isopropylimino)diethanol is used as a corrosion inhibitor in industrial processes for its ability to form stable complexes with metal ions, thereby preventing the corrosion of metal surfaces.
Used in Chelating Agent Applications:
In industrial processes, 2,2'-(Isopropylimino)diethanol is used as a chelating agent to bind metal ions, which is crucial for processes that require the control of metal ion concentrations.
Used in Personal Care Products:
2,2'-(Isopropylimino)diethanol is used as an ingredient in personal care products due to its compatibility with skin and its ability to improve the stability and performance of formulations.
Used in Detergent Formulations:
In the detergent industry, 2,2'-(Isopropylimino)diethanol is used to enhance the cleaning power and effectiveness of detergents by chelating metal ions that can interfere with the cleaning process.
Used in Metalworking Fluids:
2,2'-(Isopropylimino)diethanol is used in metalworking fluids as a component that helps to prevent corrosion and improve the longevity of the fluids, as well as the machinery they are used with.
Used in Pharmaceutical Formulations:
Given its low toxicity and strong chelating properties, 2,2'-(Isopropylimino)diethanol is utilized in pharmaceutical formulations to improve the stability and effectiveness of certain drugs.

Check Digit Verification of cas no

The CAS Registry Mumber 121-93-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,2 and 1 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 121-93:
(5*1)+(4*2)+(3*1)+(2*9)+(1*3)=37
37 % 10 = 7
So 121-93-7 is a valid CAS Registry Number.

121-93-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[2-hydroxyethyl(propan-2-yl)amino]ethanol

1.2 Other means of identification

Product number -
Other names N-isopropyldiethanolamine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:121-93-7 SDS

121-93-7Relevant academic research and scientific papers

POLYAZACYCLIC COMPOUNDS. PART I. SYNTHESIS OF ARYLSULFONYL DERIVATIVES OF 1,4,7,10-TETRAAZACYCLODODECANE AND 1-OXA-4,7,10-TRIAZACYCLODODECANE SUBSTITUTED AT REQUIRED NITROGEN ATOMS

Sienkiewicz, Juliusz,Goss, Ewa,Stanczak, Andrzej

, p. 77 - 86 (2007/10/02)

A method of preparation of new polyazamacrocyclic compounds substituted at required nitrogen atoms is given based on the example of synthesis of the title derivatives.The method consists in the cyclocondensation of substrates, of which at least one has a tertiary amino group present in the macrocyclic compound.

Neurochemistry of aging. 1. Toxins for an animal model of Alzheimer's disease

Mistry,Abraham,Hanin

, p. 376 - 380 (2007/10/02)

A chronic deficiency in central cholinergic function has been implicated in a number of neuropsychiatric diseases including Alzheimer's disease. Until recently, animal models that simulate the neurochemical conditions that appear to cause these diseases in humans, as a result of a direct manipulation of the central cholinergic system, were not available. Over the past few years, however, we have been successful in developing a cholinotoxin, 1-ethyl-1-(2-hydroxyethyl)aziridinium chloride (AF64A), which has the potential to serve as a novel compound in developing animal models of human brain disorders in which a cholinergic hypofunction has been implicated. In this paper are described the design, synthesis, and testing of several structural analogues of AF64A as potential cholinotoxins, by evaluating them for their ability to inhibit high-affinity choline transport and their affinity toward brain muscarinic receptors. One of the compounds, 1-cyclopropyl-1-(2-hydroxyethyl)aziridinium chloride was found to have a remarkably high affinity (about 40 times higher than AF64A) toward brain muscarinic receptors.

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