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A4731312

Haloperidol , 98% , 52-86-8

Synonym(s):
4-[4-(4-Chlorophenyl)-4-hydroxy-1-piperidinyl]-1-(4-fluorophenyl)-1-butanone;4-[4-(4-Chlorophenyl)-4-hydroxypiperidino]-4′-fluorobutyrophenone;4-[4-(p-Chlorophenyl)-4-hydroxypiperidino]-4′-fluorobutyrophenone;Haloperidol

CAS NO.:52-86-8

Empirical Formula: C21H23ClFNO2

Molecular Weight: 375.86

MDL number: MFCD00051423

EINECS: 200-155-6

Pack Size Price Stock Quantity
1G RMB135.20 In Stock
5G RMB535.20 In Stock
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Update time: 2022-07-08

PRODUCT Properties

Melting point: 152 °C
Boiling point: 529.0±50.0 °C(Predicted)
Density  1.1820 (estimate)
Flash point: 9℃
storage temp.  2-8°C
solubility  45% (w/v) aq 2-hydroxypropyl-β-cyclodextrin: 0.39 mg/mL
form  powder
pka 8.3(at 25℃)
color  white
Water Solubility  2.058mg/L(22.5 ºC)
Merck  14,4598
BCS Class 4/3
CAS DataBase Reference 52-86-8(CAS DataBase Reference)
NIST Chemistry Reference Haloperidol(52-86-8)
EPA Substance Registry System Haloperidol (52-86-8)

Description and Uses

Haloperidol is a butyrophenone with a long duration of action. It has lile α- adrenoceptor blocking activity and minimal effect on the cardiovascular system. It is an effective antiemetic but has a high incidence of extrapyramidal adverse effects. Haloperidol may be used in the short-term management of the acutely agitated patient (when sinister causes of confusion such as hypoxaemia and sepsis have been excluded) and in the management of delirium in ICU. The duration of action of haloperidol is approximately 24–48h.

Antidyskinetic; antipsychotic

Safety

Symbol(GHS) 
GHS06,GHS08
Signal word  Danger
Hazard statements  H301-H315-H317-H319-H335-H361
Precautionary statements  P201-P202-P280-P301+P310-P302+P352-P305+P351+P338
Hazard Codes  T,F
Risk Statements  60-61-25-36/37/38-43-39/23/24/25-23/24/25-11
Safety Statements  53-26-36/37/39-45-36/37-16
RIDADR  UN 2811 6.1/PG 3
WGK Germany  3
RTECS  EU1575000
HazardClass  6.1(b)
PackingGroup  III
HS Code  2933399090
Hazardous Substances Data 52-86-8(Hazardous Substances Data)
Toxicity LD50 orally in rats: 165 mg/kg (Goldenthal); i.p. in mice: 60 mg/kg (Collins, Horlington)

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