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4-AMINOBUTYLPHOSPHONIC ACID is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

35622-27-6

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35622-27-6 Usage

Biochem/physiol Actions

4-aminobutylphosphonic acid, the phosphonic acid analogue of delta-aminovaleric acid, inhibits gamma-aminobutyric acid B (GABA-B receptor) binding without influencing either isoproterenol- or forskolin-stimulated cyclic AMP production.

Check Digit Verification of cas no

The CAS Registry Mumber 35622-27-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,6,2 and 2 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 35622-27:
(7*3)+(6*5)+(5*6)+(4*2)+(3*2)+(2*2)+(1*7)=106
106 % 10 = 6
So 35622-27-6 is a valid CAS Registry Number.
InChI:InChI=1/C4H12NO3P/c5-3-1-2-4-9(6,7)8/h1-5H2,(H2,6,7,8)

35622-27-6SDS

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 4-aminobutylphosphonic acid

1.2 Other means of identification

Product number -
Other names 4-Aminobutylphosphonic acid

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:35622-27-6 SDS

35622-27-6Downstream Products

35622-27-6Relevant academic research and scientific papers

ORGANOPHOSPHORUS COMPOUNDS AS POTENTIAL FUNGICIDES. PART II. AMINOALKANE-, GUANIDINOALKANE-, AND THIOUREIDOALKANE-PHOSPHONIC ACIDS: PREPARATION, SPECTROSCOPY, AND FUNGICIDAL ACTIVITY

Cameron, David G.,Hudson, Harry R.,Pianka, Max

, p. 21 - 38 (2007/10/02)

A range of α-amino-, ω-amino-, α-guanidino-, and ω-guanidinoalkanephosphonic acids has been prepared for the purpose of studying their spectroscopic features and fungicidal activity.In addition, α-thioureido-octanephosphonic acid and thioureylene-1,1-bis(1-octanephosphonic acid) were isolated during the preparation of α-guanidino-octanephosphonic acid. 31P, 1H, and 13C nmr spectral data which were obtained for solutions of the amino- and guanidino-compounds in D2O or D2O/D2SO4, and for the thioureido compounds in DMSO-d6, are discussed together with previouslyreported data for the aminophosphonic types.FAB mass spectrometry generally gives strong pseudomolecular ions + for the zwitterionic amino- and guanidino-compounds with relatively simple fragmentations.Fungicidal activity of the α-aminophosphonic acids was found to be greater than for the ω-amino compounds, with maximum activity at a chain length of three carbon atoms when used as a seed dressing for the control of Drechslera spp.Moderately good activity was shown by the thioureido compounds against a number of fungal organisms in vitro but the guanidino-compounds exhibited low activity.Key words: Organophosphorus; fungicides; aminophosphonic acids; guanidinophosphonic acids; NMR spectroscopy; FAB mass spectroscopy.

Borane Reduction of Dialkoxyphosphorylcarboxamides as a New Route to Aminoalkylphosphonic Acids

Wasielewski, Czeslaw,Dembkowski, Leszek,Topolski, Marek

, p. 52 - 53 (2007/10/02)

A new, simple method for the synthesis of aminoalkylphosphonic acids is based on the reduction of dialkoxyphosphorylcarboxamides with the borane-dimethyl sulfide complex.

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