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483-63-6

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483-63-6 Usage

Description

Different sources of media describe the Description of 483-63-6 differently. You can refer to the following data:
1. 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.
2. 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

Different sources of media describe the Uses of 483-63-6 differently. You can refer to the following data:
1. N-Ethyl-o-crotonotoluidide (Crotamiton) was used to treat scabies and various pruritic dermatoses.
2. antipruritic, scabicide
3. 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.

Check Digit Verification of cas no

The CAS Registry Mumber 483-63-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,8 and 3 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 483-63:
(5*4)+(4*8)+(3*3)+(2*6)+(1*3)=76
76 % 10 = 6
So 483-63-6 is a valid CAS Registry Number.
InChI:InChI=1/C13H17NO/c1-4-8-13(15)14(5-2)12-10-7-6-9-11(12)3/h4,6-10H,5H2,1-3H3/b8-4+

483-63-6 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (H59183)  Crotamiton, 97%   

  • 483-63-6

  • 1g

  • 76.0CNY

  • Detail
  • Alfa Aesar

  • (H59183)  Crotamiton, 97%   

  • 483-63-6

  • 5g

  • 262.0CNY

  • Detail
  • Sigma-Aldrich

  • (C2970000)  Crotamiton  European Pharmacopoeia (EP) Reference Standard

  • 483-63-6

  • C2970000

  • 1,880.19CNY

  • Detail
  • USP

  • (1151006)  Crotamiton  United States Pharmacopeia (USP) Reference Standard

  • 483-63-6

  • 1151006-200MG

  • 4,647.24CNY

  • Detail

483-63-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name crotamiton

1.2 Other means of identification

Product number -
Other names N-ethylcrotono-o-toluidide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:483-63-6 SDS

483-63-6Synthetic route

N-ethyl-N-(2-methylphenyl)but-2-enamide
483-63-6

N-ethyl-N-(2-methylphenyl)but-2-enamide

N-ethyl-N-(2-methylphenyl)butanamide

N-ethyl-N-(2-methylphenyl)butanamide

Conditions
ConditionsYield
With O,N-bis-(trifluoroacetyl)-hydroxylamine; hydroxylamine In 1,4-dioxane; water at 140℃; for 0.333333h;

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483-63-6Downstream Products

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