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94-24-6

  • Product Name:Tetracaine
  • Molecular Formula:C15H24N2O2
  • Molecular Weight:264.368
  • Appearance:White crystalline powder
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Product Details

pd_meltingpoint:41.0 to 45.0 °C

Appearance:White crystalline powder

Purity:99%

Quality products make an important contribution to long-term revenue and profitability. Good Supplier In China Fast Delivery Tetracaine 94-24-6 new batch stock

1.What is the Tetracaine ?

White or light-yellow, waxy solid. Very slightly soluble in water; soluble in alcohol, ether, benzene, chloroform.

ChEBI: A benzoate ester in which 4-N-butylbenzoic acid and 2-(dimethylamino)ethanol have combined to form the ester bond; a local ester anaesthetic (ester caine) used for surface and spinal anaesthesia.

Tetracaine is a local anesthetic or numbing medicine that is used to numb the throat, eyes, or nose. Normally, the drug is administered before starting a surgery to decrease pain from the procedure. Tetracaine is applied to the eyes 30 minutes before the start of an intravenous and its effects can last up to 15 minutes.

2.What is the CAS number for Tetracaine ?

The CAS number of Tetracaine is 94-24-6.

3.What are another words for Tetracaine ?

Synonyms for Tetracaine 94-24-6:Benzoicacid, p-(butylamino)-, 2-(dimethylamino)ethyl ester (8CI);2-Dimethylaminoethylp-butylaminobenzoate;Amethocaine;Ametop;Anetain;Butylocaine;Contralgin;Fissucain;Intercain;Laudocaine;Medicaine;Medihaler-Tetracaine;Meethobalm;Metraspray;Mucaesthin;Pontocaine;Rexocaine;Uromucaesthin;b-Dimethylaminoethylp-N-butylaminobenzoate;b-Dimethylaminoethyl p-butylaminobenzoate;

4.What is Tetracaine (94-24-6) used for?

Tetracaine, also known as amethocaine, is the most potent and lipidsoluble ester local anaesthetic and has significant potential for toxicity if used systemically. It is commonly used as a 4% gel for topical application to decrease the pain from venous puncture or cannulation.

InChI:InChI=1/C15H24N2O2/c1-4-5-10-16-14-8-6-13(7-9-14)15(18)19-12-11-17(2)3/h6-9,16H,4-5,10-12H2,1-3H3

Relevant articles related to Tetracaine:

Article

Source

A new method of dicaine synthesis from p-nitrobenzoic acid ethylate

Abdullaev

, p. 28 - 31 (2002)

Preparation method of tetracaine hydrochloride

-

, (2017/04/22)

Block of cyclic nucleotide-gated channels by tetracaine derivatives: Role of apolar interactions at two distinct locations

Strassmaier, Timothy,Kirk, Sarah R.,Banerji, Tapasree,Karpen, Jeffrey W.

, p. 645 - 649 (2008/09/19)

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