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28537-85-1

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28537-85-1 Usage

General Description

Octanoic acid, compound with dibutylamine (1:1) is a chemical compound that consists of equal parts of octanoic acid and dibutylamine. Octanoic acid, also known as caprylic acid, is a saturated fatty acid commonly found in coconut oil and is used in the production of various products such as soaps and cosmetics. Dibutylamine is an organic compound that is commonly used as an intermediate in the production of herbicides, insecticides, and rubber chemicals. When combined in a 1:1 ratio, octanoic acid and dibutylamine form a compound that has various potential applications, including as a corrosion inhibitor, a lubricant additive, and as a surfactant in industrial processes.

Check Digit Verification of cas no

The CAS Registry Mumber 28537-85-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,5,3 and 7 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 28537-85:
(7*2)+(6*8)+(5*5)+(4*3)+(3*7)+(2*8)+(1*5)=141
141 % 10 = 1
So 28537-85-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H19N.C8H16O2/c1-3-5-7-9-8-6-4-2;1-2-3-4-5-6-7-8(9)10/h9H,3-8H2,1-2H3;2-7H2,1H3,(H,9,10)

28537-85-1SDS

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 N-butylbutan-1-amine,octanoic acid

1.2 Other means of identification

Product number -
Other names -

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:28537-85-1 SDS

28537-85-1Downstream Products

28537-85-1Relevant articles and documents

Supramolecular polymer gels formed from carboxy-terminated telechelic polybutadiene and polyamidine through amidinium-carboxylate salt bridge

Furusho, Yoshio,Endo, Takeshi

, p. 1815 - 1824 (2014/06/09)

In this article, we report the preparation and properties of the bulk supramolecular polymer gels prepared from a polybutadiene based on the amidinium-carboxylate salt bridge, highlighting the difference from a well-established network system based on carboxylic acid and amine. We have prepared the amidinium-carboxylate salt bridge-based supramolecular polymer gels from a carboxy-terminated telechelic polybutadiene and a linear polyamidine having N,N′-di-substituted acetamidine group in the main chain. FTIR analysis along with Small angle X-ray scattering measurements indicated that the salt bridge was attributed to the gelation through three-dimensional network formation. Virtually no fluidity was observed for the supramolecular gel containing equimolar amounts of the carboxyl group and the amidine group, which showed a high G′ value of about 1 MPa at room temperature and a T gel of 37 C. For comparison, the supramolecular polymer gels crosslinked by ammonium-carboxylate salt were prepared using a linear polyethyleneimine instead of the polyamidine. The gel with equimolar amounts of the carboxyl group and the secondary amino group showed liquid-like fluidity with a G′ value of about 0.01 MPa at room temperature, which was attributed to the fact that a certain amount of the carboxyl group remained as its free form without salt formation, as evidenced by FTIR analysis. Copyright

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