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2-[4-(2-Hydroxyethyl)-1-piperazinyl]nicotinic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 111855-51-7 Structure
  • Basic information

    1. Product Name: 2-[4-(2-Hydroxyethyl)-1-piperazinyl]nicotinic acid
    2. Synonyms: 2-[4-(2-Hydroxyethyl)-1-piperazinyl]nicotinic acid;2-(4-(2-HYDROXYETHYL)PIPERAZIN-1-YL)NICOTINIC ACID
    3. CAS NO:111855-51-7
    4. Molecular Formula: C12H17N3O3
    5. Molecular Weight: 251.28168
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 111855-51-7.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-[4-(2-Hydroxyethyl)-1-piperazinyl]nicotinic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-[4-(2-Hydroxyethyl)-1-piperazinyl]nicotinic acid(111855-51-7)
    11. EPA Substance Registry System: 2-[4-(2-Hydroxyethyl)-1-piperazinyl]nicotinic acid(111855-51-7)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: IRRITANT
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 111855-51-7(Hazardous Substances Data)

111855-51-7 Usage

General Description

2-[4-(2-Hydroxyethyl)-1-piperazinyl]nicotinic acid, also known as PIPN, is a chemical compound that belongs to the class of nicotinic acid derivatives. It is a derivative of niacin, which is a B vitamin that plays a crucial role in maintaining healthy skin and nerves. PIPN is commonly used as a chelating agent and is known for its ability to complex with metal ions. It has been studied for potential applications in areas such as pharmacology and in the treatment of metal intoxication. Additionally, PIPN has also been investigated for its potential as a corrosion inhibitor in various industrial applications due to its ability to form stable complexes with metal ions.

Check Digit Verification of cas no

The CAS Registry Mumber 111855-51-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,8,5 and 5 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 111855-51:
(8*1)+(7*1)+(6*1)+(5*8)+(4*5)+(3*5)+(2*5)+(1*1)=107
107 % 10 = 7
So 111855-51-7 is a valid CAS Registry Number.

111855-51-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[4-(2-Hydroxyethyl)-1-piperazinyl]nicotinic acid

1.2 Other means of identification

Product number -
Other names -

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:111855-51-7 SDS

111855-51-7Downstream Products

111855-51-7Relevant articles and documents

Pharmacologically active alkylol derivatives

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, (2008/06/13)

New alkylol derivatives are described, which belong to the class having the structure formula STR1 where R represents a 5 or 6 membered heterocyclic ring selected among pyridine, pyrimidine, pyrazine, pyridazine, thiophene, furan, thiazole which optionally may be substituted with one or more groups selected among alkyl, alkoxy, halogen, amide, hydroxy, methylthio, trifluoromethyl, cyano, carboxy and the corresponding alkyl esters and salts with alkali metals n is 2 X and X' represent each a hydrogen atom or hydroxy group with the exception of both being hydrogen atom, and X' may be hydroxyethoxy moiety m is 0 or 1 and the corresponding non-toxic pharmaceutically acceptable acid addition salts. The compounds of the formula I are endowed with an interesting antitussive activity and, at their active dose, practically they are free of undesired side effects.

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