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N-PENTYL-4-AMINOBENZOATE, also known as ethyl aminobenzoate or benzocaine, is a local anesthetic and pain reliever that is commonly used in over-the-counter products such as creams, ointments, and sprays. It works by numbing the skin and mucous membranes, providing temporary relief from pain and discomfort. N-PENTYL-4-AMINOBENZOATE is generally considered safe for topical use when applied as directed, but should not be ingested or used in large quantities as it can cause serious side effects. Overall, N-PENTYL-4-AMINOBENZOATE is a widely used and effective ingredient in various topical pain relief products.

13110-37-7

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13110-37-7 Usage

Uses

Used in Topical Pain Relief Products:
N-PENTYL-4-AMINOBENZOATE is used as a local anesthetic and pain reliever for providing temporary relief from pain and discomfort associated with minor skin irritations, itching, insect bites, and sunburn.
Used in Over-the-Counter Products:
N-PENTYL-4-AMINOBENZOATE is used as an active ingredient in over-the-counter products such as creams, ointments, and sprays for its numbing effect on the skin and mucous membranes.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, N-PENTYL-4-AMINOBENZOATE is used as a key component in the formulation of various topical pain relief medications, helping to alleviate minor aches and pains.
Used in Cosmetic Industry:
N-PENTYL-4-AMINOBENZOATE is also used in the cosmetic industry for its soothing and numbing properties, particularly in products designed to provide relief from skin irritations and discomfort.

Check Digit Verification of cas no

The CAS Registry Mumber 13110-37-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,1,1 and 0 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 13110-37:
(7*1)+(6*3)+(5*1)+(4*1)+(3*0)+(2*3)+(1*7)=47
47 % 10 = 7
So 13110-37-7 is a valid CAS Registry Number.
InChI:InChI=1/C12H17NO2/c1-2-3-4-9-15-12(14)10-5-7-11(13)8-6-10/h5-8H,2-4,9,13H2,1H3

13110-37-7 Well-known Company Product Price

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  • Alfa Aesar

  • (B23732)  n-Pentyl 4-aminobenzoate, 98%   

  • 13110-37-7

  • 5g

  • 456.0CNY

  • Detail
  • Alfa Aesar

  • (B23732)  n-Pentyl 4-aminobenzoate, 98%   

  • 13110-37-7

  • 25g

  • 1763.0CNY

  • Detail

13110-37-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name N-PENTYL-4-AMINOBENZOATE

1.2 Other means of identification

Product number -
Other names n-pentyl p-aminobenzoate

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:13110-37-7 SDS

13110-37-7Relevant academic research and scientific papers

Synthesis and phase behaviors of side-chain liquid-crystalline polymers containing azobenzene mesogen with the different length alkyl tail

Chen, Sheng,Ling, Aihua,Zhang, Hai-Liang

, p. 2759 - 2768 (2013)

A series of side-chain liquid-crystal polymers, poly[6-[4-(4′-n-alkyl benzoateazo)phenoxy]-hexylmethacrylate]s (PMAzoCOORm, m = 1, 2, 3, 4, 5, 6, 8, 10, 14, and 18) have been prepared by two synthetic methods. The chemical structure of the monomers was confirmed by 1H NMR and mass spectrometry. The molecular characterizations of the polymers were performed with 1H NMR and gel permeation chromatograph. The phase behaviors of polymers were investigated by the combination of techniques including differential scanning calorimetry, polarized optical microscopy, and small-angle X-ray scattering. For m = 1, 2, 3, 4, 5, and 6, the polymers exhibited a monosmectic A phase in which the smectic layer period was almost identical to the side-chain length. In addition, for m = 2, 3, 4, and 5, they presented the monosmectic C phase in low temperature; moreover, the tilt angle increased from 23.3 to 40.5°. For m = 8, 10, 14, and 18, the polymers showed a bilayer smectic A phase in which the layer spacing was larger than a fully extended side chain but less than two extended chains. On the other hand, for the clearing point, with the increasing of m, it first decreased, and then increased. All of these indicated that the length of alkyl tails played an important role in the phase behaviors of these polymers.

Synthesis and Investigation of Mesomorphic Properties of Some Thiazole Derivatives

Murza, M. M.,Golovanov, A. S.,Safarov, M. G.

, p. 1529 - 1532 (2007/10/03)

2,4-Disubstituted thiazoles with liquid crystal properties are synthesized.Influence of the length of the aliphatic chain on the type of mesomorphism and the width of the temperature range of the mesophase existence is investigated.The compounds are shown to possess mesomorphism of smectic type in the range of 36-145 deg C.

Smectogenic Salts Formed by Combination of Alkyl p-Aminobenzoates and p-Ethyl- or p-Chlorobenzenesulfonic Acid

Matsunaga, Y.,Sakamoto S.,Togashi, A.,Tsujimoto, M.

, p. 161 - 166 (2007/10/02)

Two series of smectogenic salts were obtained by combining alkyl p-aminobenzoates with p-ethyl- and p-chlorobenzenesulfonic acids, respectively.The shortest ester alkyl chain required to generate a smectic A phase is nonyl when the former sulfonic acid is employed but the chain may be as short as butyl when the latter is employed.The smectic A-isotropic transition temperature in the second series is significantly higher than that in the first series, indicating that the terminal substituent on the anion is as crucial as that in non-ionic mesogens in determining the mesophase stability. - Keywords: Smectic, alkyl p-aminobenzoates, benzenesulfonates

EFFECTS OF BRANCHING OF THE ALKYL CHAIN ON THE LIQUID CRYSTALLINE PROPERTIES OF N-(p-PHENYLBENZYLIDENE)-p-ALKOXYCARBONYLANILINES.

Matsunaga,Miyajima

, p. 353 - 359 (2007/10/02)

The liquid crystal behavior of twenty-three N-(p-phenylbenzylidene)-p-alkoxycarbonylanilines has been examined by optical microscopy and differential scanning calorimetry in order to study the effects of branching of the alkyl groups.

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