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Propylguanidine, also known as 1-(3-aminopropyl)guanidine, is an organic compound with the chemical formula C5H13N5. It is a derivative of guanidine, featuring a propyl group attached to the guanidine moiety. Propylguanidine is a colorless liquid with a pungent odor and is soluble in water. It is used as a chemical intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. Due to its reactivity, it is essential to handle propylguanidine with care, as it can be harmful if inhaled, ingested, or absorbed through the skin.

462-25-9

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462-25-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 462-25-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,6 and 2 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 462-25:
(5*4)+(4*6)+(3*2)+(2*2)+(1*5)=59
59 % 10 = 9
So 462-25-9 is a valid CAS Registry Number.
InChI:InChI=1/C4H11N3/c1-2-3-7-4(5)6/h2-3H2,1H3,(H4,5,6,7)

462-25-9SDS

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 2-propylguanidine

1.2 Other means of identification

Product number -
Other names N-Propyl-Guanidine Hemi-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:462-25-9 SDS

462-25-9Relevant academic research and scientific papers

Continuous synthesis method of hydroxypyrimidine compound

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Paragraph 0012; 0032, (2020/07/28)

The invention discloses a continuous synthesis method of a hydroxypyrimidine compound. The method comprises the steps: carrying out continuous reaction on organic amine and a 50% cyanamide aqueous solution in a micro-reactor, introducing the reaction solution into a liquid separator for continuous phase splitting, carrying out continuous ring closing on a guanidine solution and alpha-alkyl acetoacetate in a second micro-reactor, washing the reaction solution with water, and desolventizing to obtain a target product. The method is based on the concept of green chemistry, the comprehensive costof raw materials is far lower than that of traditional methods, no salt-containing wastewater is generated, and treatment is easy; traditional solid-liquid separation is avoided, automatic productionis facilitated, and the safety and environmental protection level of the device is improved; continuous synthesis is adopted, decomposition of an intermediate is avoided, the total yield is larger than 82%, and the product content reaches 98%.

PHARMACOLOGICALLY ACTIVE GUANIDINE COMPOUNDS

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, (2008/06/13)

The compounds are substituted thioalkyl-, aminoalkyl-and oxyalkyl-guanidines which are inhibitors of histamine activity.

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