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Dicaine, also known as benzocaine, is a local anesthetic chemical compound that is commonly used to provide temporary relief from pain and itching caused by various skin conditions, such as insect bites, sunburn, and minor cuts. It works by blocking nerve signals in the affected area, thus numbing the sensation of pain. Benzocaine is available in various forms, including creams, ointments, gels, and sprays, and is often used in over-the-counter medications. However, it is important to note that it should not be used on open wounds or broken skin, as it may cause further irritation or complications. Additionally, some individuals may experience an allergic reaction to benzocaine, so it is crucial to consult a healthcare professional before using it, especially for children.

3772-42-7

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3772-42-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3772-42-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,7 and 2 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3772-42:
(6*3)+(5*7)+(4*7)+(3*2)+(2*4)+(1*2)=97
97 % 10 = 7
So 3772-42-7 is a valid CAS Registry Number.
InChI:InChI=1/C17H28N2O2/c1-4-7-12-18-16-10-8-15(9-11-16)17(20)21-14-13-19(5-2)6-3/h8-11,18H,4-7,12-14H2,1-3H3

3772-42-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(diethylamino)ethyl 4-(butylamino)benzoate

1.2 Other means of identification

Product number -
Other names 2'-Dimethylaminoaethyl-4-butylamino-benzoat

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:3772-42-7 SDS

3772-42-7Downstream Products

3772-42-7Relevant academic research and scientific papers

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)

A series of new tetracaine derivatives was synthesized to explore the effects of hydrophobic character on blockade of cyclic nucleotide-gated (CNG) channels. Increasing the hydrophobicity at either of two positions on the tetracaine scaffold, the tertiary amine or the butyl tail, yields blockers with increased potency. However, shape also plays an important role. While gradual increases in length of the butyl tail lead to increased potency, substitution of the butyl tail with branched alkyl or cyclic groups is deleterious.

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