289876
Ethylphosphonic acid
98%
Synonym(s):
P-Ethylphosphonic acid
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All Photos(3)
About This Item
Linear Formula:
C2H5P(O)(OH)2
CAS Number:
Molecular Weight:
110.05
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Assay
98%
mp
61-63 °C (lit.)
SMILES string
CCP(O)(O)=O
InChI
1S/C2H7O3P/c1-2-6(3,4)5/h2H2,1H3,(H2,3,4,5)
InChI key
GATNOFPXSDHULC-UHFFFAOYSA-N
Related Categories
General description
The synthesis of novel nucleotide analogs based on phosphonic acids from ethylphosphonic acid was studied.
Application
Ethylphosphonic acid was used as an internal standard in the determination of fosfomycin in human plasma.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Skin Corr. 1B
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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Theodora A Papakondyli et al.
Journal of chromatography. A, 1332, 1-7 (2014-02-11)
An analytical method employing novel sample preparation and liquid chromatography coupled with atmospheric pressure chemical ionization mass spectrometric detection (LC-APCI/MS) was developed for the determination of fosfomycin in human plasma. Sample preparation involves derivatization through phase transfer catalysis (PTC) which
Stefanie Klein et al.
Small (Weinheim an der Bergstrasse, Germany), 14(21), e1704111-e1704111 (2018-04-19)
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Adarsh Gandhi et al.
Biomedical chromatography : BMC, 32(6), e4214-e4214 (2018-02-21)
Extensive use and misuse of antibiotics over the past 50 years has contributed to the emergence and spread of antibiotic-resistant bacterial strains, rendering them as a global health concern. To address this issue, a dynamic in vitro hollow-fiber system, which mimics
E V Efimtseva et al.
Bioorganicheskaia khimiia, 24(1), 16-20 (1998-04-29)
The synthesis of novel nucleotide analogues on the basis of ethylphosphonic acid was described. A rigid structural element, an amide or a double bond, was characteristics of the compounds synthesized. The antiviral and cytotoxic activities of these compounds were studied
Jonna E Teikari et al.
The ISME journal, 12(6), 1619-1630 (2018-02-16)
Nodularia spumigena is a nitrogen-fixing cyanobacterium that forms toxic blooms in the Baltic Sea each summer and the availability of phosphorous is an important factor limiting the formation of these blooms. Bioinformatic analysis identified a phosphonate degrading (phn) gene cluster
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