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2-AMINO-4,6-DINITROBENZENEMETHANOL, also known as 2,4-Dinitro-6-hydroxybenzylamine, is a chemical compound characterized by its molecular formula C7H7N3O5. It presents as a yellow to brown crystalline solid, which is notable for its use in the synthesis of dyes, pharmaceuticals, and agrochemicals. Additionally, it serves as an intermediate in the production of various organic compounds. Due to its explosive and toxic properties, 2-AMINO-4,6-DINITROBENZENEMETHANOL requires careful handling and storage to ensure safety for both humans and the environment.

226711-13-3

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226711-13-3 Usage

Uses

Used in Chemical Synthesis Industry:
2-AMINO-4,6-DINITROBENZENEMETHANOL is used as a key intermediate for the synthesis of dyes, which are essential for coloring textiles, plastics, and other materials. Its unique chemical structure allows for the creation of a wide range of colorants with specific properties.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, 2-AMINO-4,6-DINITROBENZENEMETHANOL is utilized as a precursor in the development of various medicinal compounds. Its reactivity and functional groups make it a valuable component in the synthesis of drugs with specific therapeutic effects.
Used in Agrochemical Industry:
2-AMINO-4,6-DINITROBENZENEMETHANOL is employed as a building block in the production of agrochemicals, such as pesticides and herbicides. Its chemical properties contribute to the effectiveness of these products in controlling pests and weeds in agricultural settings.
Used in Organic Compounds Production:
As an intermediate, 2-AMINO-4,6-DINITROBENZENEMETHANOL is crucial for the synthesis of a variety of organic compounds used in different industries. Its versatility in chemical reactions enables the creation of specialized compounds for specific applications.
Safety and Handling:
Due to the explosive and toxic nature of 2-AMINO-4,6-DINITROBENZENEMETHANOL, it is imperative to follow proper safety protocols during its production, storage, and use. This includes implementing measures to prevent accidental exposure and ensuring that the compound is handled and stored in a controlled environment to minimize risks to human health and the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 226711-13-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,6,7,1 and 1 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 226711-13:
(8*2)+(7*2)+(6*6)+(5*7)+(4*1)+(3*1)+(2*1)+(1*3)=113
113 % 10 = 3
So 226711-13-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H7N3O5/c8-6-1-4(9(12)13)2-7(10(14)15)5(6)3-11/h1-2,11H,3,8H2

226711-13-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-amino-4,6-dinitrophenyl)methanol

1.2 Other means of identification

Product number -
Other names Benzenemethanol,2-amino-4,6-dinitro

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:226711-13-3 SDS

226711-13-3Downstream Products

226711-13-3Relevant academic research and scientific papers

Synthesis of reference substances for highly polar metabolites of nitroaromatic compounds

Schmidt, Torsten C.,Steinbach, Klaus,Buetehorn, Ulf,Heck, Kerstin,Volkwein, Ute,Stork, Gottfried

, p. 3119 - 3130 (2007/10/03)

Transformation processes of nitroaromatic compounds (NAC) lead to polar and highly hydrophilic metabolites. For the unequivocal identification of proposed metabolites reference substances are needed. Since most of them are not commercially available, their synthesis was done in our group. In many cases no satisfying synthesis schemes were found in the literature. In this communication, we therefore describe the preparation, structural elucidation and separation of 17 compounds. Many of the newly synthesized analytes were found in various water samples from a former ammunition plant.

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