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HYDROXYLAMINE PHOSPHATE is a white crystalline powder that serves as a versatile chemical compound with various applications across different industries.

20845-01-6

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20845-01-6 Usage

Uses

Used in Chemical Synthesis:
HYDROXYLAMINE PHOSPHATE is used as a reactant for the aqueous preparation of rhenium diphosphate, which is an important compound in the field of chemistry.
Used in Gas and Solid State Reactions:
HYDROXYLAMINE PHOSPHATE is used as a reactant in gas and solid state reactions with acetone, contributing to the synthesis of various chemical products.
Used in Hydroxylamine Formation:
HYDROXYLAMINE PHOSPHATE is used as a reactant for the formation of hydroxylamine via photolysis, a process that involves the decomposition of a compound by light.

Biochem/physiol Actions

MAO inhibitor; inhibits platelet aggregation

Check Digit Verification of cas no

The CAS Registry Mumber 20845-01-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,8,4 and 5 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 20845-01:
(7*2)+(6*0)+(5*8)+(4*4)+(3*5)+(2*0)+(1*1)=86
86 % 10 = 6
So 20845-01-6 is a valid CAS Registry Number.

20845-01-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name HYDROXYLAMINE PHOSPHATE

1.2 Other means of identification

Product number -
Other names HAP

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:20845-01-6 SDS

20845-01-6Downstream Products

20845-01-6Relevant academic research and scientific papers

Joint production technology of hydroxylamine, hydroxylammonium salt and cyclohexanone-oxime

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Paragraph 0012; 0024; 0025; 0034; 0035, (2017/09/26)

The invention discloses a joint production technology of hydroxylamine, hydroxylammonium salt and cyclohexanone-oxime. The material comprises the steps that reaction liquid obtained by raw materials through an ammoximation reaction and a hydrooximation reaction is extracted and separated to obtain an organic phase, the organic phase is prepared into product cyclohexanone-oxime, or part of the organic phase and part of product cyclohexanone-oxime are adopted as raw materials for an oxime hydrolysis reaction to be hydrolyzed, the organic phase in hydrolysis liquid is circulated to return to a oximation reactor, part of an inorganic phase in the hydrolysis liquid is adopted as a raw material to be circulated to return to a hydroxylamine oximation reactor, and the other part of the inorganic phase is prepared into a hydroxylamine aqueous solution and hydroxylammonium salt. The joint production technology of hydroxylamine, hydroxylammonium salt and cyclohexanone-oxime is simple in procedure, the requirement of the ammoximation reaction for the purity of the raw material cyclohexanone and the catalyst performance is lowered, a high quality cyclohexanone-oxime product without cyclohexanone is obtained, the simplification of the downstream caprolactam technology and the improvement of the product quality are benefited, and the hydroxylamine and hydroxylammonium salt product which have high additional value are obtained simultaneously.

Recycling system for hydroxylamine formation and oximation

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Page/Page column 4-5, (2008/12/06)

A recycling system for hydroxylamine formation and oximation is proposed. The recycling system includes a hydroxylamine formation zone, an oximation zone, a purification zone, and an adjusting zone having a nitrate absorption tower. An inorganic process s

THE INFRARED SPECTRUM OF THE HYDROXYLAMINE DIMER

Yeo, G. A.,Ford, T. A.

, p. 307 - 324 (2007/10/02)

The infrared spectra of the hydroxylamine monomer and dimer, trapped in nitrogen and argon matrices at ca. 17 K, have been obtained.Assignments have been made, based on concentration and matrix diffusion experiments, and the wavenumber shifts arising from

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