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1,3-Benzenediol, 4-nonyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

18979-67-4

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18979-67-4 Usage

Molecular weight

236.36 g/mol

Chemical structure

A benzene ring with two hydroxyl (OH) groups at the 1 and 3 positions, and a nonyl (C9H19) group attached to the 4 position.

Family

Phenolic compounds

Applications

a. Intermediate in the production of antioxidants, dyes, and lubricating oils
b. Surfactant in industrial processes
c. Emulsifier in various applications
d. Dispersing agent in the manufacturing of various products

Environmental impact

Persistent organic pollutant

Health concerns

Disrupts endocrine function in animals and humans

Regulatory status

Increasingly being regulated and restricted in many countries due to environmental and health risks

Check Digit Verification of cas no

The CAS Registry Mumber 18979-67-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,9,7 and 9 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 18979-67:
(7*1)+(6*8)+(5*9)+(4*7)+(3*9)+(2*6)+(1*7)=174
174 % 10 = 4
So 18979-67-4 is a valid CAS Registry Number.

18979-67-4Relevant academic research and scientific papers

Antifungal Activity of 2,4-Dihydroxyacylophenones and Related Compounds

Mizobuchi, Shigeyuki,Sato, Yuko

, p. 1327 - 1334 (2007/10/02)

The antifungal activity of 2,4-dihydroxyacylophenones and related compounds against Trichophyton spp. and other fungi were investigated to determine their structure-activity relationships.The activity of these compounds was found to be closely related to the length of the acyl and alkyl substituents attached to the 1,3-dihydroxybenzene moiety.In addition, differences in activity were observed depending on the position of the alkyl substituents and on the number of substituents attached to the 1,3-dihydroxybenzene moiety.Some compounds tested showed potent antifungal activity against Trichophyton spp. and other fungi that was more active than amphotericin B.

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