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Hydroxylamine, O,O'-1,2-ethanediylbis-, dihydrochloride is a chemical compound formed by two hydroxylamine molecules connected through an ethylene bridge and two chloride ions. It is known for its role in organic and inorganic synthesis, particularly in the preparation of oximes and hydroxamic acids. As a reducing agent, it is instrumental in the production of pharmaceuticals, dyes, and other organic compounds. The dihydrochloride form enhances its solubility in water, facilitating its use in various chemical reactions. However, it requires careful handling due to its potential hazards.

104845-83-2

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104845-83-2 Usage

Uses

Used in Organic and Inorganic Synthesis:
Hydroxylamine, O,O'-1,2-ethanediylbis-, dihydrochloride is used as a reagent for the preparation of oximes and hydroxamic acids, which are important intermediates in the synthesis of various organic and inorganic compounds.
Used in Pharmaceutical Production:
In the pharmaceutical industry, Hydroxylamine, O,O'-1,2-ethanediylbis-, dihydrochloride serves as a reducing agent in the synthesis of various drugs, contributing to the development of new medications and therapeutic agents.
Used in Dye Production:
Hydroxylamine, O,O'-1,2-ethanediylbis-, dihydrochloride is utilized as a reducing agent in the production of dyes, playing a crucial role in the synthesis of colorants for various applications, including textiles, plastics, and printing inks.
Used in Other Organic Compounds Production:
Hydroxylamine, O,O'-1,2-ethanediylbis-, dihydrochloride is also employed in the synthesis of other organic compounds, where its reducing properties are harnessed to facilitate the formation of desired products in chemical reactions.

Check Digit Verification of cas no

The CAS Registry Mumber 104845-83-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,8,4 and 5 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 104845-83:
(8*1)+(7*0)+(6*4)+(5*8)+(4*4)+(3*5)+(2*8)+(1*3)=122
122 % 10 = 2
So 104845-83-2 is a valid CAS Registry Number.

104845-83-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2-bis(aminooxy)ethane dihydrochloride

1.2 Other means of identification

Product number -
Other names 1,2-bis(aminooxy)ethane hydrochloride

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:104845-83-2 SDS

104845-83-2Relevant articles and documents

Synthesis of novel adamantylalkoxyurea derivatives from 2-(1-adamantylimino)-1,3-oxathiolane

Shirayev, Andrey,Iin, Paul Kong Thoo,Moiseev, Igor K.

, p. 38 - 40 (1997)

2-(1-Adamantylimino)-5-methyl-1,3-oxathiolane 1 was synthesised from the reaction between adamantan-1-ol and 1-thiocyanopropan-2-ol in sulphuric acid. Compound 1 undergoes ring opening followed by elimination to afford novel adamantane alkoxyureas 3a-d an

Alternating Copolymerization of CO2and Cyclohexene Oxide Catalyzed by Cobalt-Lanthanide Mixed Multinuclear Complexes

Asaba, Hiroki,Deng, Jingyuan,Hatazawa, Masahiro,Iwasaki, Takanori,Mashima, Kazushi,Nagae, Haruki,Nozaki, Kyoko

, p. 7928 - 7933 (2020)

Heteromultimetallic complexes consisting of three Co(II) ions and one lanthanide ion were synthesized and applied to the alternating copolymerization of CO2 and cyclohexene oxide. Unlike the conventional cobalt(III) salen complexes, the high thermal stabi

Tandem Functionalization in a Highly Branched Polymer with Layered Structure

Cao, Xiaosong,Shi, Yi,Gan, Weiping,Gao, Haifeng

, p. 5974 - 5981 (2018)

A hyperbranched polymer with multilayer structure was developed to demonstrate the possibility of highly efficient tandem functionalization reactions at different domains within one nanostructured platform. The polymer scaffold was constructed by chain-growth copper-catalyzed azide–alkyne cycloaddition polymerization of three functional monomers with sequential monomer addition in one pot. Subsequent reactions with different monomer units resulted in efficient functionalization of each segment with construction of a highly sophisticated polymer structure by a robust procedure. As a proof of concept, the ability of this polymer structure to quantitatively load six species of guest molecules through three different types of conjugation reactions was demonstrated.

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