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532-34-3

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532-34-3 Usage

Description

BUTOPYRONOXYL, also known as Indalon, is a yellow to pale reddish-brown liquid with an aromatic odor. It is reasonably stable in air and slowly affected by light. This chemical compound is insoluble in water but miscible with alcohol, chloroform, ether, and glacial acetic acid.

Uses

Used in Insect Repellent Industry:
BUTOPYRONOXYL is used as an insect repellent for providing protection against insects when applied directly on the skin. Its effectiveness in repelling insects makes it a valuable component in the development of insect repellent products.
Used in Chemical Industry:
BUTOPYRONOXYL, due to its chemical properties, can be utilized in various applications within the chemical industry. Its miscibility with different solvents allows for its use in the formulation of various products, such as paints, coatings, and adhesives. Additionally, its stability in air and resistance to light exposure make it suitable for use in applications where long-lasting performance is required.

Synthesis

To a 25-mL flflame-dried flflask under a nitrogen atmosphere were added freshly distilled Rawal’s diene (227 mg, 1 mmol, 1.0 equivalents) and 2 mL of CHCl3. Benzaldehyde (1.5 mmol, 1.5 equivalents) was added dropwise via a gas-tight syringe. The reaction mixture was stirred at room temperature for 2 h and then diluted with 15 mL of CH2Cl2. The yellow solution was cooled to ?78 °C and treated with 142 μL acetyl chloride (2 mmol, 2 equivalents). After stirring for about 30 min, saturated Na2CO3 was added. The organic layer was separated and the water phase was diluted with 15 mL of water and extracted twice with CH2Cl2. The combined organic phase was dried with MgSO4, fifiltered, and concentrated to give a yellow oil, which was subjected to flflash chromatography to afford the desired dihydropyrone in 86% overall yield. Reference: Huang, Y.; Rawal, V. H. Org. Lett. 2000, 2, 3321?3322.

Indications

Butopyronoxyl is not water soluble and can be applied to skin and clothing to repel biting stable flies, Lone Star ticks, dog and cat fleas, and chiggers.

Hazard

Toxic by ingestion. May cause liver dam- age.

Safety Profile

Moderately toxic by ingestion. Produces liver necrosis in experimental animals. A rmld skin irritant. See also OXALATES and ESTERS. Combustible when exposed to heat or flame. When heated to decomposition it emits acrid fumes.

Check Digit Verification of cas no

The CAS Registry Mumber 532-34-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,3 and 2 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 532-34:
(5*5)+(4*3)+(3*2)+(2*3)+(1*4)=53
53 % 10 = 3
So 532-34-3 is a valid CAS Registry Number.
InChI:InChI=1/C12H18O4/c1-4-5-6-15-11(14)10-7-9(13)8-12(2,3)16-10/h7H,4-6,8H2,1-3H3

532-34-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name butopyronoxyl

1.2 Other means of identification

Product number -
Other names INDALONE

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:532-34-3 SDS

532-34-3Upstream product

532-34-3Relevant articles and documents

Pesticide compositions and method

-

, (2008/06/13)

Toxicant, especially pesticide compositions, having lowered dermal toxicity are provided. The compositions include a lipophilic-pesticide, a nonionic surfactant and a dry inert diluent carrier. Methods for reducing the dermal toxicity of lipophilic toxicants, especially pesticides are provided, as well as methods for controlling insect pests using the disclosed compositions.

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