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(2,6-dibromo-4-methylphenoxy)acetic acid, also known as bromoxynil, is a synthetic herbicide compound designed to control broadleaf weeds in agricultural settings. It functions by inhibiting photosynthesis in the target plants, ultimately leading to their death. Bromoxynil is characterized by its low environmental persistence and rapid degradation, which helps to minimize its impact on non-target organisms. However, it is crucial to adhere to label instructions and safety guidelines to mitigate potential risks to aquatic life and beneficial insects.

38206-97-2

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38206-97-2 Usage

Uses

Used in Agricultural Industry:
(2,6-dibromo-4-methylphenoxy)acetic acid is used as a herbicidal agent for controlling broadleaf weeds in crop fields. It is particularly effective due to its ability to inhibit photosynthesis in the target plants, leading to their death. To enhance its effectiveness, bromoxynil is often formulated as a mixture with other herbicides. The low persistence and rapid degradation of this chemical in the environment contribute to its reduced impact on non-target organisms, making it a preferred choice for weed management in agriculture.

Check Digit Verification of cas no

The CAS Registry Mumber 38206-97-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,2,0 and 6 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 38206-97:
(7*3)+(6*8)+(5*2)+(4*0)+(3*6)+(2*9)+(1*7)=122
122 % 10 = 2
So 38206-97-2 is a valid CAS Registry Number.

38206-97-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2,6-dibromo-4-methylphenoxy)acetic acid

1.2 Other means of identification

Product number -
Other names <2,6-Dibrom-4-methyl-phenyloxy>-essigsaeure

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:38206-97-2 SDS

38206-97-2Relevant academic research and scientific papers

Design, Synthesis, and Testing of Potential Antisickling Agents. 4. Structure-Activity Relationships of Benzyloxy and Phenoxy Acids

Abraham, D. J.,Kennedy, P. E.,Mehanna, A. S.,Patwa, D. C.,Williams, F. L.

, p. 967 - 978 (2007/10/02)

In this paper we further establish the activity of two classes of small molecules, benzyloxy and phenoxy acids, as potent inhibitors of hemoglobin S (HbS) gelation.Structural modifications with a large number of each class confirm our earlier work that the highest activity is observed with compounds that contain dihalogenated aromatic rings with attached polar side chains.We have also found a halogenated aromatic malonic acid derivative to be quite active.Compounds reported in this paper are compared with other antigelling agents studied in our laboratory.Comments are made concerning the antigelling activity and binding sites of four derivatives and their effect on the allosteric mechanism of hemoglobin (Hb) function.

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