Crotamiton Property

Melting point:

25°C

Boiling point:

153-155 °C/13 mmHg (lit.)

Density 

0.987 g/mL at 25 °C (lit.)

refractive index 

n20/D 1.54(lit.)

Flash point:

>230 °F

storage temp. 

2-8°C

solubility 

ethanol: soluble

pka

1.14±0.50(Predicted)

form 

<25°C Solid,>25°C Liquid

color 

Colourless to Light Brown

Water Solubility 

Soluble in water (1:500), alcohol, methanol, ether, and ethanol.

Merck 

13,2622

Stability:

Light Sensitive

InChIKey

DNTGGZPQPQTDQF-XBXARRHUSA-N

LogP

3.099 (est)

CAS DataBase Reference

483-63-6(CAS DataBase Reference)

NIST Chemistry Reference

Crotamiton(483-63-6)

EPA Substance Registry System

Crotamiton (483-63-6)

Safety

Hazard Codes 

Xn

Risk Statements 

22-36/38-43

Safety Statements 

26-36

WGK Germany 

3

RTECS 

GQ7000000

HS Code 

2924296000

Hazard and Precautionary Statements (GHS)

Symbol(GHS)

Signal word

Warning

Hazard statements

H302Harmful if swallowed

Precautionary statements

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P270Do not eat, drink or smoke when using this product.

P301+P312IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.

P501Dispose of contents/container to..…

Crotamiton Chemical Properties,Usage,Production

Description

Crotamiton is available as a 10% cream for the treatment of scabies, although it is less effective than pyrethrins or permethrin. Because crotamiton may need to be applied a second time for successful treatment of scabies but the pyrethrins or permethrin require a single application, poor patient compliance with crotamiton may reduce its effectiveness. The advantage of crotamiton over lindane comes from the fact that lindane has potential neurotoxicity if absorbed especially in infants and children, whereas crotamiton has less systemic neurotoxicity.

Description

Crotamiton is an ectoparasiticide and antipruritic agent. It blocks the mouse transient receptor potential vanilloid 4 (TRPV4) channel expressed in HEK293 cells in a calcium-dependent manner (IC₅₀s = 223.5 and 15.5 μM in buffer containing 0 and 2 mM calcium, respectively). It inhibits scratching behavior in mice induced by the TRPV4 agonist GSK1016790A . Topical application of crotamiton (0.025 g of a 10% ointment) also inhibits scratching behavior in mice induced by histamine, serotonin , and the proteinase-activated receptor 2 (PAR2) agonist SLIGRL-NH₂ . Formulations containing crotamiton have been used to eradicate scabies and in the treatment of symptomatic pruritic skin.

Chemical Properties

N-Ethyl-o-crotonotoluidide is colourless or pale yellow, oily liquid

Originator

Eurax,Ciba Geigy,France,1949

Uses

N-Ethyl-o-crotonotoluidide (Crotamiton) was used to treat scabies and various pruritic dermatoses.

Uses

antipruritic, scabicide

Uses

Fungicide, insecticide.

Definition

ChEBI: The amide resulting from the formal condensation of crotonic acid with N-ethyl-2-methylaniline. A colourless or pale yellow oily liquid, it is used in the treatment of pruritus (itching) by producing a counter-irritation: as it evaporate from the skin, it produces a cooling effect that diverts attention away from the itching. It has also been used as an acaricide in the treatment of scabies, though more effective drugs are usually preferred.

Indications

Crotamiton (N-ethyl-o-crotonotoluide, Eurax) is a synthetic chloroformate salt used for the prevention and treatment of scabies, although cure rates tend to be lower for the same number of applications compared with lindane and permethrin. It may have an antipruritic effect independent of its scabetic effect. Its mechanism of action is unknown. It is not effective as a pediculicide.
Crotamiton (10% N-ethyl-o-crotonotoluide, Eurax) cream applied twice and left on during a 48-hour period is usually effective against scabies and has been reported to act as an antipruritic agent.

Manufacturing Process

10.5 parts of crotonyl chloride are dropped in such a manner into 27 parts of N-ethyl-o-toluidine, white stirring, that the temperature rises to 130° to 140°C. After cooling, the reaction product is dissolved in ether or other solvent that is immiscible with water, and the solution is washed successively with hydrochloric acid, alkali solution and water. After distilling off the solvent, the residue is distilled in vacuo. The crotonic acid N-ethyl-o-toluidide boils at 153° to 155°C at a pressure of 13 mm and is a slightly yellowish oil. Instead of carrying the reaction out in the presence of an excess of N-ethyl-otoluidine, it may be carried out in the presence of an acid-combining agent, for example, potash, advantageously in a solvent (e.g., acetone).

brand name

Eurax (Westwood-Squibb).

Therapeutic Function

Scabicide

Clinical Use

N-Ethyl-N-(2-methylphenyl)-2-butenamide, or N-ethyl-ocrotonotoluidide(Eurax), is a colorless, odorless oily liquid.It is virtually insoluble in water but soluble in most organicsolvents.
Crotamiton is available in 10% concentration in a lotionand a cream intended for the topical treatment of scabies. Its antipruritic effect is probably because of a local anestheticaction.

Side effects

The most common side effect reported for crotamiton is skin irritation.

Veterinary Drugs and Treatments

Crotamiton is a topical miticide/scabicide and has been used primarily for adjunctive treatment (with ivermectin) for treating mite infections (e.g., Knemidopkoptes) in birds. Crotamiton has both miticidal and antipruritic actions, but the mechanism for each is not known.