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PIPERIDINE-1-CARBOXAMIDINE HEMISULFATE is a versatile chemical compound that serves as a hemisulfate salt of the amine, piperidine, and the carboxamide, carboxamidine. It is widely recognized for its role as a reagent in organic synthesis and as a building block in the production of pharmaceuticals and agrochemicals.

17238-53-8

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17238-53-8 Usage

Uses

Used in Pharmaceutical Industry:
PIPERIDINE-1-CARBOXAMIDINE HEMISULFATE is used as a key building block for the synthesis of various pharmaceuticals. Its unique chemical structure allows it to be incorporated into a wide range of drug molecules, contributing to the development of new and effective treatments for various medical conditions.
Used in Agrochemical Industry:
In the agrochemical industry, PIPERIDINE-1-CARBOXAMIDINE HEMISULFATE is utilized as a fundamental component in the creation of various agrochemicals. Its properties make it suitable for use in the development of pesticides, herbicides, and other agricultural chemicals that help protect crops and enhance agricultural productivity.
Used in Organic Synthesis:
PIPERIDINE-1-CARBOXAMIDINE HEMISULFATE is used as a reagent in organic synthesis, where it plays a crucial role in the formation of various organic compounds. Its versatility allows it to be employed in a multitude of chemical reactions, facilitating the synthesis of a broad spectrum of organic molecules.
Used in Dye Production:
PIPERIDINE-1-CARBOXAMIDINE HEMISULFATE is used as a starting material in the production of dyes. Its chemical properties enable it to be transformed into a variety of dye molecules, which are then utilized in various industries, such as textiles, printing, and cosmetics.
Used in Polymer Synthesis:
In the field of polymer science, PIPERIDINE-1-CARBOXAMIDINE HEMISULFATE is employed as a monomer or a building block in the synthesis of polymers. Its incorporation into polymer chains can impart specific properties to the resulting polymers, making them suitable for various applications, such as coatings, adhesives, and plastics.
Used in Surfactant Production:
PIPERIDINE-1-CARBOXAMIDINE HEMISULFATE is also used in the production of surfactants. Its amphiphilic nature allows it to be incorporated into surfactant molecules, which are then used in a wide range of applications, including detergents, emulsifiers, and dispersants.

Check Digit Verification of cas no

The CAS Registry Mumber 17238-53-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,2,3 and 8 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 17238-53:
(7*1)+(6*7)+(5*2)+(4*3)+(3*8)+(2*5)+(1*3)=108
108 % 10 = 8
So 17238-53-8 is a valid CAS Registry Number.
InChI:InChI=1/2C6H13N3.H2O4S/c2*7-6(8)9-4-2-1-3-5-9;1-5(2,3)4/h2*1-5H2,(H3,7,8);(H2,1,2,3,4)

17238-53-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name piperidine-1-carboximidamide,sulfuric acid

1.2 Other means of identification

Product number -
Other names piperidine-1-carboxamidine,sulfate

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:17238-53-8 SDS

17238-53-8Relevant academic research and scientific papers

Ultrasound-assisted synthesis of substituted guanidines using 1H-pyrazole-1-carboxamidine and S-methylisothiouronium sulfate under solvent-free conditions

Fujita, Mitsue,Furusho, Yoshio

, p. 4339 - 4342 (2018/07/06)

We have investigated ultrasound-assisted synthesis of guanidine derivatives using 1H-Pyrazole-1-carboxamidine (PyzCA) and S-substituted isothiouronium sulfate (MeITU). The guanylations of several amines are promoted by ultrasound sonication under solvent-free conditions, and proceed under mild conditions. It is of particular interest that the guanylations do not require bases in most cases.

Synthesis of substituted indole derivatives as a new class of antimalarial agents

Agarwal, Anu,Srivastava, Kumkum,Puri,Chauhan, Prem M.S.

, p. 3133 - 3136 (2007/10/03)

A series of substituted indole derivatives were synthesized and evaluated for their in vitro antimalarial activity against P. falciparum. Out of the 24 compounds synthesized six compounds have shown MIC of 1 μg/mL. These compounds are in vitro several fol

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