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40898-94-0

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40898-94-0 Usage

Description

1-Amino-1-propanol, also known as Amino-1-propyl alcohol or simply aminopropanol, is an organic compound with the chemical formula NH2-CH2-CH2-CH2-OH. It is a colorless liquid with a mild amine-like odor and is soluble in water. 1-Amino-1-propanol is characterized by the presence of an amino group (-NH2) attached to a three-carbon chain with a hydroxyl group (-OH) at the end, making it a versatile building block in various chemical reactions and applications.

Uses

1. Used in Chemical Synthesis:
1-Amino-1-propanol is used as a reagent for the preparation of nanocomposites, which are materials with unique properties due to the combination of nanoparticles and a polymer matrix. These nanocomposites have a wide range of applications, including in electronics, energy storage, and environmental protection.
2. Used in Pharmaceutical Industry:
1-Amino-1-propanol is used as a reagent in the synthesis of N-substituted fagomine derivatives, which are known to display α-glycosidase inhibition. α-Glycosidase inhibitors are important in the pharmaceutical industry as they can help manage blood sugar levels in patients with diabetes by slowing down the breakdown of carbohydrates in the body.
3. Used in Surface Treatment:
1-Amino-1-propanol can be used in the surface treatment of various materials, such as metals and plastics, to improve their properties, such as adhesion, corrosion resistance, and biocompatibility.
4. Used in Personal Care Products:
Due to its mild amine-like odor and solubility in water, 1-Amino-1-propanol can be used in the formulation of personal care products, such as shampoos, conditioners, and body washes, to provide a pleasant scent and improve the product's performance.
5. Used in Laboratory Research:
1-Amino-1-propanol is also used in laboratory research as a solvent or reagent for various chemical reactions, including the synthesis of pharmaceuticals, dyes, and other specialty chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 40898-94-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,8,9 and 8 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 40898-94:
(7*4)+(6*0)+(5*8)+(4*9)+(3*8)+(2*9)+(1*4)=150
150 % 10 = 0
So 40898-94-0 is a valid CAS Registry Number.

40898-94-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2S-amino-1-propanol

1.2 Other means of identification

Product number -
Other names 1-amino-2-propanol

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:40898-94-0 SDS

40898-94-0Relevant articles and documents

Synthesis method of 2-aminopropanol

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Paragraph 0047-0048; 0050-0051, (2020/04/29)

The invention discloses a synthesis method of 2-aminopropanol. According to the method, epoxypropane and liquid ammonia are taken as raw materials, epoxypropane and liquid ammonia are introduced intoa fixed bed reactor, the molar ratio of epoxypropane to liquid ammonia is 1: (5-20), and under the action of a rare earth modified catalyst, reaction is carried out for 10-60s at the temperature of 100-200 DEG C, so that 2-aminopropanol is obtained. The method is reasonable in process, simple and convenient to operate, high in atom economy and low in emission of three wastes, and meets the requirements of industrial production.

Kinetic study of the reaction between iodide and N-chloramines

Antelo, J. M.,Arce, F.,Campos, J.,Parajo, M.

, p. 391 - 396 (2007/10/03)

We carried out a kinetic study of the reaction between iodide ion and various primary N-chloramines and found it to be first-order in the latter.Experiments also showed the rate constant for the reaction to be directly proportional to the iodide and hydrogen ion concentrations.The influence of the concentration reveals the presence of general acid catalysis processes.

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