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113422-79-0

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113422-79-0 Usage

Chemical composition

1-Tetradecanol, 4-aminobenzoate is composed of a long-chain alcohol (1-tetradecanol) and an amino derivative of benzoic acid (4-aminobenzoate).

Physical properties of 1-tetradecanol

1-tetradecanol is a white, waxy solid.

Industrial applications of 1-tetradecanol

It is used in the production of detergents, lubricants, and surfactants.

Physical properties of 4-aminobenzoate

4-aminobenzoate is a crystalline powder.

Uses of 4-aminobenzoate

It is commonly used in the manufacture of pharmaceuticals and as a UV filter in sunscreen products.

Potential uses of 1-tetradecanol, 4-aminobenzoate combination

It may have potential uses in the formulation of personal care products, pharmaceuticals, and other chemical applications.

Check Digit Verification of cas no

The CAS Registry Mumber 113422-79-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,4,2 and 2 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 113422-79:
(8*1)+(7*1)+(6*3)+(5*4)+(4*2)+(3*2)+(2*7)+(1*9)=90
90 % 10 = 0
So 113422-79-0 is a valid CAS Registry Number.

113422-79-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-aminobenzoic acid,tetradecan-1-ol

1.2 Other means of identification

Product number -
Other names tetradecyl 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:113422-79-0 SDS

113422-79-0Downstream Products

113422-79-0Relevant articles and documents

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

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