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118-95-6

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118-95-6 Usage

Description

DNPP, or 2,6-dinitro-4-phenylphenol, is a chemical compound known for its antimicrobial properties and is used as a preservative in various industries. It is effective against a wide range of microorganisms, including bacteria and fungi. However, it has been identified as a potential environmental pollutant and poses health risks due to its toxicity. As a result, it is listed as a hazardous substance by various regulatory bodies, and its use and handling are restricted in many countries.

Uses

Used in Wood Preservation Industry:
DNPP is used as a preservative in the wood preservation industry to protect wood from decay and damage caused by fungi and bacteria. Its antimicrobial properties help maintain the structural integrity and longevity of wooden materials.
Used in Fungicide and Bactericide Formulation:
DNPP is used as an active ingredient in fungicide and bactericide formulations to control the growth of microorganisms in various applications, such as agriculture, horticulture, and industrial settings. Its broad-spectrum antimicrobial activity makes it effective against a wide range of pathogens.
Used as a Topical Antiseptic:
DNPP is used as a topical antiseptic to prevent infection in minor cuts, wounds, and burns. Its antimicrobial properties help to kill or inhibit the growth of bacteria and fungi, promoting faster healing and reducing the risk of infection.
However, due to its potential environmental and health risks, the use of DNPP must be carefully regulated to minimize its impact on human health and the environment. Regulatory bodies have imposed restrictions on its use and handling, and alternative preservatives with lower toxicity and environmental impact are being sought to replace DNPP in various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 118-95-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,1 and 8 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 118-95:
(5*1)+(4*1)+(3*8)+(2*9)+(1*5)=56
56 % 10 = 6
So 118-95-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H10N2O5/c1-5(2)7-3-6(10(13)14)4-8(9(7)12)11(15)16/h3-5,12H,1-2H3

118-95-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-dinitro-6-propan-2-ylphenol

1.2 Other means of identification

Product number -
Other names Phenol,2,4-dinitro-6-isopropyl

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:118-95-6 SDS

118-95-6Upstream product

118-95-6Relevant articles and documents

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Dutton et al.

, p. 685 (1953)

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2-OXY-4H-3,1-BENZOXAZIN-4-ONES AND PHARMACEUTICAL USE

-

, (2008/06/13)

2-Oxy-4H-3,1-benzoxazin-4-ones represented by the formula: STR1 and the pharmaceutically acceptable acid addition salts thereof, wherein: a is an integer of 0-4;A is a bond, or alkylene having one to eight carbon atoms;R is hydrogen, phenyl, imidazolyl or cycloalkyl having three to six carbon atoms, wherein the phenyl, imidazolyl or cycloalkyl ring is optionally substituted with 1-3 substituents independently selected from the group consisting of lower alkyl having one to four carbon atoms, lower alkoxy having one to four carbon atoms,--N(R 1) 2,--NO 2, halo or lower alkylthio having one to four carbon atoms, and, each R' is independently selected from the group consisting of lower alkyl having one to six atoms, lower alkenyl having two to six carbon atoms, lower alkoxy having one to six carbon atoms, lower alkylthio or halo-lower alkyl having one to four carbon atoms, halo,--NO 2,--N(R 1) 2, STR2--NR 1 COR 2, and STR3 in which each R 1 is independently hydrogen or lower alkyl having one to four carbon atoms, or together form a piperidine or a piperazine ring optionally substituted at the ring nitrogen by lower alkyl having one to four carbon atoms or--CH 2 CH 2 OH, each R 2 is independently lower alkyl having one to four carbon atoms, A is an alkylene group if R is hydrogen, and the pharmaceutically acceptable acid addition salts thereof are useful as serine protease inhibitors in humans and animals.

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