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A2471812

Chlorpheniramine Maleate , ≥99% , 113-92-8

Synonym(s):
(±)-Chlorpheniramine maleate salt;Chlorpheniramine maleate solution

CAS NO.:113-92-8

Empirical Formula: C20H23ClN2O4

Molecular Weight: 390.86

MDL number: MFCD00069225

EINECS: 204-037-5

Pack Size Price Stock Quantity
5G RMB41.60 In Stock
25G RMB67.20 In Stock
100G RMB203.20 In Stock
500G RMB711.20 In Stock
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Update time: 2022-07-08

PRODUCT Properties

Melting point: 130-135 °C (lit.)
alpha  -1~+1°(D/20℃)(c=5,DMF)
Density  1.1984 (rough estimate)
refractive index  1.6800 (estimate)
Flash point: 9℃
storage temp.  2-8°C
solubility  Freely soluble in water, soluble in ethanol (96 per cent)
form  Solid
color  White to Almost white
Odor odorless
PH 4.0~5.5 (10g/l, 25℃)
Water Solubility  1-5 g/100 mL at 21 ºC
Merck  14,2180
BCS Class 3/1
InChIKey DBAKFASWICGISY-BTJKTKAUSA-N
LogP 3.389 (est)

Description and Uses

Chlorpheniramine is a histamine H1 receptor antagonist with an IC75 value of 0.0016 μg/ml for reversal of histamine-induced spasms in isolated guinea pig ileum. It protects against intravenous histamine-induced death (PD50 = 0.15 mg/kg) and delays induction of aerosolized histamine-induced coughing (ED100sec = 0.44 mg/kg) in guinea pigs. Chlorpheniramine (20 mg/kg, i.p.) prevents histamine-induced passive cutaneous anaphylaxis (PCA) in rabbits. It also reduces respiratory resistance and hypersecretion of tracheobronchial fluid in a dog model of histamine-induced asthma. Formulations containing chlorpheniramine have been used in the treatment of seasonal allergies.

(±)-Chlorpheniramine maleate salt has been used:

  • as H1 receptor antagonist to determine the receptor function
  • to block the effect of compound 48/80 on plasma IGF-I
  • as a standard for fast sensing and determination by sequential injector coupled with potentiometer

Safety

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H302
Precautionary statements  P301+P312+P330
Hazard Codes  T,F
Risk Statements  25-39/23/24/25-23/24/25-11
Safety Statements  36/37/39-45-36/37-16
RIDADR  UN 2811 6.1/PG 3
WGK Germany  3
RTECS  US6504000
TSCA  Yes
HazardClass  6.1(b)
PackingGroup  III
HS Code  29333990
Toxicity LD50 orally in mice: 162 mg/kg (Smith)

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