52899-59-9

Basic information

• Product Name: 4-butyl-2-nitrophenol
• Synonyms: 4-butyl-2-nitrophenol;Einecs 258-245-6
• CAS NO: 52899-59-9
• Molecular Formula: C₁₀H₁₃NO₃
• Molecular Weight: 195.21512
• EINECS: 258-245-6
• Mol File: 52899-59-9.mol

Chemical Properties

• Boiling Point: 297.6 °C at 760 mmHg
• Flash Point: 125.6 °C
• Appearance: /
• Density: 1.179g/cm³
• Vapor Pressure: 0.000752mmHg at 25°C
• Refractive Index: 1.559
• CAS DataBase Reference: 4-butyl-2-nitrophenol(CAS DataBase Reference)
• NIST Chemistry Reference: 4-butyl-2-nitrophenol(52899-59-9)
• EPA Substance Registry System: 4-butyl-2-nitrophenol(52899-59-9)

Safety Data

• Hazardous Substances Data: 52899-59-9(Hazardous Substances Data)

Usage

Uses

Used in Pesticide Industry:
4-butyl-2-nitrophenol is used as a pesticide for its toxic properties, which help control and eliminate pests. Its application in this industry is aimed at protecting crops and maintaining agricultural productivity.
Used in Insecticide Industry:
In the insecticide industry, 4-butyl-2-nitrophenol is utilized for its ability to kill insects. It is applied to control insect populations that can cause damage to crops or transmit diseases.
However, it is important to note that 4-butyl-2-nitrophenol is considered harmful if ingested, inhaled, or in contact with the skin, and can cause irritation to the respiratory system, skin, and eyes. Due to its toxicity, it is also classified as a potential environmental hazard, particularly to aquatic life. Therefore, proper handling, storage, and disposal measures should be taken to minimize its impact on human health and the environment.

InChI:InChI=1/C10H13NO3/c1-2-3-4-8-5-6-10(12)9(7-8)11(13)14/h5-7,12H,2-4H2,1H3

Upstream product

• 18272-84-9 4-n-butylanisole 
• 1638-22-8 4-n-butylphenol 

Downstream Products

• 85533-49-9 2-amino-4-n-butylphenol 
• 81259-61-2 4-Heptyl-benzoic acid 4-butyl-2-nitro-phenyl ester 
• 860570-77-0 N-(2'-hydroxy'5'-butylphenyl)acetamide 

Relevant articles and documents

Nitration method for p-alkylphenol

The invention discloses a nitration method for p-alkylphenol. The nitration method successively comprises the following steps: 1) adding the p-alkylphenol used as a raw material into a container, thenadding water and a catalyst, dropwise adding nitric acid under stirring, controlling a temperature of materials in the container not to exceed 25 DEG C in the dropwise adding process, and after the nitric acid is dropwise added, carrying out a reaction at 10 to 20 DEG C for 2 to 3 h; and 2) subjecting a reaction solution obtained in the step 1) to standing and layering, wherein the lower layer obtained by layering is a product (o-nitro-p-alkylphenol), and subjecting an upper-layer solution obtained by layering to cyclic reuse, i.e., cyclic nitration. By adoption of the method for synthesizingthe o-nitro-p-alkylphenol provided by the invention, the utilization rate of raw materials is high; cyclic reuse of waste acid and waste water is realized; the discharging of three wastes is reduced;the cost of production is lowered; meanwhile, a product has high purity, high yield and good industrial application value.

HARMFUL ARTHROPOD CONTROL COMPOSITION, AND FUSED HETEROCYCLIC COMPOUND

Disclosed is a harmful arthropod control composition comprising, as an active ingredient, a fused heterocyclic compound represented by formula (1) [wherein A1 and A2 independently represent a nitrogen atom or the like; R1 and R4 independently represent a halogen atom or the like; R2 and R3 independently represent a halogen atom or the like; R5 and R6 independently represent a linear C1-C6 hydrocarbon group which may be substituted, or the like (provided that both R5 and R6 cannot represent a hydrogen atom simultaneously); and n represents 0 or 1]. The harmful arthropod control composition has an excellent efficacy to control harmful arthropods.

HARMFUL ARTHROPOD CONTROL COMPOSITION, AND FUSED HETEROCYCLIC COMPOUND

Disclosed is a harmful arthropod control composition comprising, as an active ingredient, a fused heterocyclic compound represented by formula (1) [wherein A1 and A2 independently represent a nitrogen atom or the like; R1 and R4 independently represent a halogen atom or the like; R2 and R3 independently represent a halogen atom or the like; R5 and R6 independently represent a linear C1-C6 hydrocarbon group which may be substituted, or the like (provided that both R5 and R6 cannot represent a hydrogen atom simultaneously); and n represents 0 or 1]. The harmful arthropod control composition has an excellent efficacy to control harmful arthropods.

COMPOSITION AND METHOD FOR CONTROLLING ARTHROPOD PESTS

The present invention provides: an arthropod pests control composition comprising, as active ingredients, a condensed heterocyclic compound and a neonicotinoid compound; a method for controlling arthropod pests which comprises applying effective amounts of a condensed heterocyclic compound and a neonicotinoid compound to the arthropod pests or a locus where the arthropod pests inhabit; and so on.

COMPOSITION AND METHOD FOR CONTROLLING ARTHROPOD PESTS

The present invention provides: an arthropod pests control composition comprising, as active ingredients, a condensed heterocyclic compound and a pyrethroid compound; a method for controlling arthropod pests which comprises applying effective amounts of a condensed heterocyclic compound and a pyrethroid compound to the arthropod pests or a locus where the arthropod pests inhabit; and so on.

COMPOSITION AND METHOD FOR CONTROLLING ARTHROPOD PESTS

The present invention provides: an arthropod pests control composition comprising, as active ingredients, a condensed heterocyclic compound and pyriproxyfen; a method for controlling arthropod pests which comprises applying effective amounts of a condensed heterocyclic compound and pyriproxyfen to the arthropod pests or a locus where the arthropod pests inhabit; and so on.

COMPOSITION AND METHOD FOR CONTROLLING ARTHROPOD PESTS

The present invention provides: an arthropod pests control composition comprising, as active ingredients, a condensed heterocyclic compound and pyridalyl; a method for controlling arthropod pests which comprises applying effective amounts of a condensed heterocyclic compound and pyridalyl to the arthropod pests or a locus where the arthropod pests inhabit; and so on.

COMPOSITION AND METHOD FOR CONTROLLING ARTHROPOD PESTS

The present invention provides: an arthropod pests control composition comprising, as active ingredients, a condensed heterocyclic compound and a diamide compound; a method for controlling arthropod pests which comprises applying effective amounts of a condensed heterocyclic compound and a diamide compound to the arthropod pests or a locus where the arthropod pests inhabit; and so on.

Alkyl-substituted benzoxazinorifamycin derivative, process for preparing the same and antibacterial agent containing the same

A novel rifamycin derivative having the formula (I): STR1 wherein X1 is an alkyl group with 1 to 6 carbon atoms or a cycloalkyl group with 3 to 8 carbon atoms; X2 is a hydrogen atom or an alkyl group with 1 to 4 carbon atoms; R1 is hydrogen atom or acetyl group; A is a group represented by the formula: STR2 wherein R2 is an alkyl group with 1 to 4 carbon atoms or an alkoxyalkyl group with 2 to 6 carbon atoms and R3 is an alkyl group with 1 to 6 carbon atoms or an alkoxyalkyl group with 2 to 6 carbon atoms, or a group represented by the formula STR3 wherein STR4 is a 3 to 9 membered cyclic amino group with 2 to 8 carbon atoms, R4 is a hydrogen atom or an alkyl group having 1 to 4 carbon atoms, or salts thereof, a process for preparing the same and antibacterial agents containing the same as an effective ingredient. The rifamycin derivative of the present invention having the formula (I) shows a strong antibacterial activity against the Gram-positive bacteria and the acid-fast bacteria.