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Details

Stereochemistry ACHIRAL
Molecular Formula C7H17O3P
Molecular Weight 180.1818
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DIISOPROPYL METHYLPHOSPHONATE

SMILES

CC(C)OP(C)(=O)OC(C)C

InChI

InChIKey=WOAFDHWYKSOANX-UHFFFAOYSA-N
InChI=1S/C7H17O3P/c1-6(2)9-11(5,8)10-7(3)4/h6-7H,1-5H3

HIDE SMILES / InChI

Molecular Formula C7H17O3P
Molecular Weight 180.1818
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Indirect laser-induced fluorescence detection for capillary electrophoresis using a violet diode laser.
2001 Apr 15
Detection and classification characteristics of arrays of carbon black/organic polymer composite chemiresistive vapor detectors for the nerve agent simulants dimethylmethylphosphonate and diisopropylmethylphosponate.
2001 Mar 1
Organophosphorus pesticides markedly inhibit the activities of natural killer, cytotoxic T lymphocyte and lymphokine-activated killer: a proposed inhibiting mechanism via granzyme inhibition.
2002 Apr 2
Toxicity of diisopropyl methylphosphonate (DIMP) to aquatic organisms.
2002 Feb
The effects of diisopropylmethylphosphonate, a by-product of the production of sarin and a contaminant in drinking water at the Rocky Mountain Arsenal, on female mink.
2003 Apr
The effects of diisopropylmethylphosphonate on female mink: how medical intervention biased mortality data.
2003 Dec
Acute toxicity of isopropyl methylphosphonic acid, a breakdown product of sarin, to eggs and fry of golden shiner and channel catfish.
2005 Jan 22
An allegation of scientific misconduct in the Bucci et al. article concerning the effects of DIMP on mink.
2005 Mar-Apr
Flexible carbon nanotube sensors for nerve agent simulants.
2006 Aug 28
Fluctuating asymmetry and condition in golden shiner (Notemigonus crysoleucas) and channel catfish (Ictalurus punctatus) reared in sublethal concentrations of isopropyl methylphosphonic acid.
2006 Jan
Screening of nerve agent degradation products by MALDI-TOFMS.
2006 Jul 1
Commentary on the allegation of scientific misconduct charge against Bucci et al.
2006 Oct
Reactive desorption electrospray ionization for selective detection of the hydrolysis products of phosphonate esters.
2007 Aug
Derivatization of organophosphorus nerve agent degradation products for gas chromatography with ICPMS and TOF-MS detection.
2007 Jun
Chemical agent identification by field-based attenuated total reflectance infrared detection and solid-phase microextraction.
2007 Mar 15
Activation of the binuclear metal center through formation of phosphotriesterase-inhibitor complexes.
2007 Mar 20
Analysis of chemical warfare agents in food products by atmospheric pressure ionization-high field asymmetric waveform ion mobility spectrometry-mass spectrometry.
2007 Nov 1
In situ infrared aerosol spectroscopy for a variety of nerve agent simulants using flow-through photoacoustics.
2007 Sep 1
Electro membrane isolation of nerve agent degradation products across a supported liquid membrane followed by capillary electrophoresis with contactless conductivity detection.
2008 Dec 19
Ultraviolet Raman spectra and cross-sections of the G-series nerve agents.
2008 Oct
Real-time trace detection and identification of chemical warfare agent simulants using recent advances in proton transfer reaction time-of-flight mass spectrometry.
2009 Dec
Determination of nerve agent degradation products by capillary electrophoresis using field-amplified sample stacking injection with the electroosmotic flow pump and contactless conductivity detection.
2009 Jul 31
Phosphonate analogues of cyclopropavir phosphates and their E-isomers. Synthesis and antiviral activity.
2009 Jun 1
The coupling of direct analysis in real time ionization to Fourier transform ion cyclotron resonance mass spectrometry for ultrahigh-resolution mass analysis.
2010 Mar
Substance Class Chemical
Created
by admin
on Sat Dec 16 02:15:46 GMT 2023
Edited
by admin
on Sat Dec 16 02:15:46 GMT 2023
Record UNII
56V3OG5DC7
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
DIISOPROPYL METHYLPHOSPHONATE
Systematic Name English
Code System Code Type Description
PUBCHEM
3073
Created by admin on Sat Dec 16 02:15:46 GMT 2023 , Edited by admin on Sat Dec 16 02:15:46 GMT 2023
PRIMARY
HSDB
6864
Created by admin on Sat Dec 16 02:15:46 GMT 2023 , Edited by admin on Sat Dec 16 02:15:46 GMT 2023
PRIMARY
ECHA (EC/EINECS)
215-896-0
Created by admin on Sat Dec 16 02:15:46 GMT 2023 , Edited by admin on Sat Dec 16 02:15:46 GMT 2023
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WIKIPEDIA
DIISOPROPYL METHYLPHOSPHONATE
Created by admin on Sat Dec 16 02:15:46 GMT 2023 , Edited by admin on Sat Dec 16 02:15:46 GMT 2023
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FDA UNII
56V3OG5DC7
Created by admin on Sat Dec 16 02:15:46 GMT 2023 , Edited by admin on Sat Dec 16 02:15:46 GMT 2023
PRIMARY
DRUG BANK
DB02127
Created by admin on Sat Dec 16 02:15:46 GMT 2023 , Edited by admin on Sat Dec 16 02:15:46 GMT 2023
PRIMARY
CHEBI
77325
Created by admin on Sat Dec 16 02:15:46 GMT 2023 , Edited by admin on Sat Dec 16 02:15:46 GMT 2023
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CAS
1445-75-6
Created by admin on Sat Dec 16 02:15:46 GMT 2023 , Edited by admin on Sat Dec 16 02:15:46 GMT 2023
PRIMARY
EPA CompTox
DTXSID5024051
Created by admin on Sat Dec 16 02:15:46 GMT 2023 , Edited by admin on Sat Dec 16 02:15:46 GMT 2023
PRIMARY