118-95-6

Basic information

• Product Name: DNPP
• Synonyms: DNPP;2-ISOPROPYL-4,6-DINITROPHENOL;4,6-DINITRO-2-ISOPROPYLPHENOL
• CAS NO: 118-95-6
• Molecular Formula: C₉H₁₀N₂O₅
• Molecular Weight: 226.19
• EINECS: 249-592-4
• Mol File: 118-95-6.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 302.8 °C at 760 mmHg
• Flash Point: 127.5 °C
• Appearance: Colourless or light yellow transparent
• Density: 1.399 g/cm³
• Vapor Pressure: 0.000538mmHg at 25°C
• Refractive Index: 1.601
• CAS DataBase Reference: DNPP(CAS DataBase Reference)
• NIST Chemistry Reference: DNPP(118-95-6)
• EPA Substance Registry System: DNPP(118-95-6)

Safety Data

• Hazardous Substances Data: 118-95-6(Hazardous Substances Data)

Usage

General Description

DNPP, or 2,6-dinitro-4-phenylphenol, is a chemical compound that is used as a preservative in various industries, including wood preservation, fungicide and bactericide formulation, and as a topical antiseptic. It is known for its antimicrobial properties and is effective against a wide range of microorganisms, including bacteria and fungi. However, DNPP has been cited as a potential environmental pollutant and poses health risks due to its toxicity. It is listed as a hazardous substance by various regulatory bodies, and there are restrictions on its use and handling in many countries. Therefore, its usage and exposure need to be carefully regulated to minimize its impact on human health and the environment.

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

Upstream product

• 88-69-7 2-(1-methylethyl)phenol 

Downstream Products

• 29506-72-7 2-Benzyloxy-1-isopropyl-3,5-dinitro-benzene 
• 29506-76-1 2-(2,4-Dichloro-benzyloxy)-1-isopropyl-3,5-dinitro-benzene 
• 874527-21-6 2-bromo-1-isopropyl-3,5-dinitro-benzene 
• 719298-83-6 2-isopropyl-4,6-dinitro-aniline 
• 26075-29-6 Cyclobutancarbonsaeure-2'-isopropyl-4',6'-dinitrophenylester 
• 29506-75-0 2-(3,4-Dichloro-benzyloxy)-1-isopropyl-3,5-dinitro-benzene 
• 29506-74-9 2-(4-Chloro-benzyloxy)-1-isopropyl-3,5-dinitro-benzene 
• 29516-74-3 1-Isopropyl-3,5-dinitro-2-prop-2-ynyloxy-benzene 
• 29516-73-2 2-Allyloxy-1-isopropyl-3,5-dinitro-benzene 
• 26065-65-6 Cyclopropancarbonsaeure-2'-isopropyl-4',6'-dinitrophenylester 
• 29506-73-8 2-(2,3-Dibromo-propoxy)-1-isopropyl-3,5-dinitro-benzene 
• 26075-34-3 Cyclopentancarbonsaeure-2'-isopropyl-4',6'-dinitrophenylester 
• 29516-75-4 2-(2-Chloro-allyloxy)-1-isopropyl-3,5-dinitro-benzene 
• 29516-65-2 2-Ethoxy-1-isopropyl-3,5-dinitro-benzene 

Relevant articles and documents

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

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.