PIPERAZINE

PRODUCT IDENTIFICATION

CAS NO.

110-85-0

PIPERAZINE 

EINECS NO. 203-808-3
FORMULA NHCH2CH2NHCH2CH2
MOL WT. 86.14

H.S. CODE

2933.59.9500

TOXICITY

Oral, rat LD50: 1900 mg/kg
SYNONYMS
Diethylenediamine; Diethyleneimine; Dispermine;

Antiren; Hexahydropyrazine; Piperazidine; Pipersol; Pyrazine hexahydride; Uvilon; 1,4-Diazacyclohexane; 1,4-Piperazine; 1,4-Diethylenediamine; Piperazin (German); N,N-Diethylenediamine; Hexahydro-1,4-diazine; Piperazidine; Pyrazine hexahydrate; Piperazin (German); Piperazina (Spanish); Pipérazine (French); Other RN: 8017-90-1, 8027-81-4, 81546-15-8, 854880-15-2, 861800-35-3

SMILES

C1CNCCN1

CLASSIFICATION

Piperazine, Anthelmintic

EXTRA NOTES

 

PHYSICAL AND CHEMICAL PROPERTIES

PHYSICAL STATE
White flake Ammonia like odor
MELTING POINT 108 C
BOILING POINT 145 - 146 C
SPECIFIC GRAVITY

1.1

SOLUBILITY IN WATER 150 g/l at 20 C
SOLVENT SOLUBILITY Freely soluble in glycerol
VAPOR DENSITY

3.0

AUTOIGNITION

340 C

pKa 9.73 (Dissociation Constant at 25 C)
log P -1.50E+00 (Octanol-water)
VAPOR PRESSURE 0.16 (mmHg at 25 C)
HENRY LAW CONSTANT 2.20E-09 (atm-m3/mole at 25 C)
OH RATE CONSTANT 1.69E-10 (cm3/molecule-sec at 25 C Atmospheric)
NFPA RATINGS Health: 2 ; Flammability: 2 ; Reactivity: 0

REFRACTIVE INDEX

 
FLASH POINT

 

STABILITY

Stable under ordinary conditions

EXTERNAL LINKS & GENERAL DESCRIPTION

Wikipedia Linking

Material Safety Data Sheet

Google Scholar Search

Drug Information Portal (U.S. National Library of Medicine) - Piperazine

http://www.chemistrydaily.com/
Piperazine is a six-sided organic ring compound containing two opposing nitrogen atoms (see image). The piperazines are a broad class of chemical compounds, all of which contain a piperazine functional group. Piperazines were originally named because of their chemical similarity with piperidine, a constiuent of piperine in the black pepper plant (Piper nigrum). This has led to the erroneous belief that piperazines are naturally derived from black pepper. In reality, no piperazines occur naturally; they are usually artificially synthesized by reacting alcoholic ammonia with 1,2-dichloroethane. Many piperazines are successful drugs. Notable piperazine drugs include:
BZP (recreational drug)
Dramamine (motion sickness drug)
Viagra (impotence drug)
A large number of piperazine compounds have anthelmintic (anti-parasitic) action. Their mode of action is generally by paralysing parasites, which allows the host body to easily remove or expel the invading organism. Piperazine hydrate and piperazine citrate are the main anthelminthic piperazines. These drugs are often referred to simply as "piperazine" which may cause confusion between the specific anthelmintic drugs and the entire class of piperazine-containing compounds. Piperazines are also used in the manufacture of plastics, resins, pesticides, and other industrial materials.

Local:
Piperazine is a heterocyclic compound containing four carbon atoms and two of nitrogen at 1,4 position ( als called 1,4-hexahydropyrazine). It is a deliquescent crystalline compound melting at 105 C; soluble in water, alcohol, glycerol, and glycols. It is used as a main ingredient of anthelmintics used to treat intestinal roundworms (ascariasis) infection in human and  poultry and to treat pinworms (enterobiasis; oxyuriasis) by altering cell membrane permeability and causing hyperpolarization of the membrane. Piperazine is a main moiety in psychoactive drugs. Certain piperazine derivatives are suspected of ecstasy substitutes. Benzylpiperazine is bannaed in many countries. Benzylpiperazine  has been used as a anthelmintic (antiparastic effect). Nitrogen in piperazine ring plays an important role in biological research and drug manufacturing industry including the preparation of anthelmintic, antiallergenic, antibacterial, antihistamic, antiemetic and antimigraine agents. The piperazine ring and piperazine derivatives are important cyclic components in industrial field as raw materials for hardener of epoxy resins, corrosion inhibitors, insecticides, accelerators for rubber, urethane catalysts and antioxidants.

SALES SPECIFICATION
APPEARANCE
White flake

PURITY

99.5% min

WATER

0.5% max

INDIVIDUAL IMPURITY

0.5% max

TRANSPORTATION
PACKING
25kgs in bag
HAZARD CLASS 8 (Packing Group: III)
UN NO. 2579
SAFETY INFORMATION

GHS

 

SIGNAL WORD Warning

PICTOGRAMS

HAZARD STATEMENTS

H314:  Causes severe skin burns and eye damage
H317:  May cause an allergic skin reaction
H334:  May cause allergy or asthma symptoms or breathing difficulties if inhaled
H361fd:  Suspected of damaging fertility. Suspected of damaging the unborn child
H228:  Flammable solid

PRECAUTIONARY STATEMENTS

P301 + P330 + P331:  IF SWALLOWED: rinse mouth. Do NOT induce vomiting
P305 + P351 + P338:  IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing
P261:  Avoid breathing dust/fume/gas/mist/vapors/spray
P304 + P341:  IF INHALED: If breathing is difficult, remove to fresh air and keep at rest in a position comfortable for breathing
P342 + P311:  If experiencing respiratory symptoms: Call a POISON CENTER or doctor/physician
P280:  Wear eye protection/face protection
P273:  Avoid release to the environment

EC DIRECTIVES

 

HAZARD CODES

F Highly flammable
C Corrosive
XN Harmful

RISK PHRASES

11:  Highly flammable.
34:  Causes burns.
42/43:  May cause sensitisation by inhalation and skin contact.
62:  Possible risk of impaired fertility.
63:  Possible risk of harm to the unborn child.

SAFETY PHRASES

22: Do not breathe dust.
26:
In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
36/37/39:
Wear suitable protective clothing, gloves and eye/face protection.
45;
In case of accident or if you feel unwell, seek medical advice immediately (show label where possible)
61: Avoid release to the environment. Refer to special instructions safety data sheet.
PRICE INFORMATION