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ChemicalBook > Product Catalogue >Chemical Reagents >Organic reagents >Aromatic acids >(4-METHYL-PIPERAZIN-1-YL)-ACETIC ACID

(4-METHYL-PIPERAZIN-1-YL)-ACETIC ACID

(4-METHYL-PIPERAZIN-1-YL)-ACETIC ACID Structure
  • ₹0
  • Product name: (4-METHYL-PIPERAZIN-1-YL)-ACETIC ACID
  • CAS: 54699-92-2
  • MF: C7H14N2O2
  • MW: 158.2
  • EINECS:
  • MDL Number:MFCD03444554
  • Synonyms:1-Piperazineaceticacid,4-methyl-(9CI);(4-METHYL-PIPERAZIN-1-YL)-ACETIC ACID >98%;1-Piperazineacetic acid, 4-Methyl-;N-(Carboxymethyl)-N'-methylpiperazine;(Carboxymethyl)-N'-methylpiperazine ;2-(4-METHYLPIPERAZIN-1-YL)ACETIC ACID;AKOS BB-5221;AKOS BBS-00002665
Manufacturer Product number Product description Packaging Price Updated Buy

Properties

Melting point :130-133°C
Boiling point :278℃
Density :1.123
Flash point :122℃
storage temp. :Sealed in dry,Room Temperature
form :solid
pka :1.85±0.10(Predicted)
color :Off-white
CAS DataBase Reference :54699-92-2(CAS DataBase Reference)

Safety Information

Symbol(GHS): GHS hazard pictograms
Signal word: Warning
Hazard statements:
Code Hazard statements Hazard class Category Signal word Pictogram P-Codes
H315 Causes skin irritation Skin corrosion/irritation Category 2 Warning GHS hazard pictograms P264, P280, P302+P352, P321,P332+P313, P362
H319 Causes serious eye irritation Serious eye damage/eye irritation Category 2A Warning GHS hazard pictograms P264, P280, P305+P351+P338,P337+P313P
Precautionary statements:
P264 Wash hands thoroughly after handling.
P264 Wash skin thouroughly after handling.
P280 Wear protective gloves/protective clothing/eye protection/face protection.
P302+P352 IF ON SKIN: wash with plenty of soap and water.
P305+P351+P338 IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
P332+P313 IF SKIN irritation occurs: Get medical advice/attention.
P337+P313 IF eye irritation persists: Get medical advice/attention.

Description

(Carboxymethyl)-N''-methylpiperazine acts as a potential antibacterial compound, due to its nocathiacin analog.

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