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About This Item
Empirical Formula (Hill Notation):
C5H15N2O4P
CAS Number:
Molecular Weight:
198.16
NACRES:
NA.24
PubChem Substance ID:
eCl@ss:
39110524
UNSPSC Code:
41116107
EC Number:
278-636-5
MDL number:
Beilstein/REAXYS Number:
8163399
grade
analytical standard
Quality Level
product line
PESTANAL®
shelf life
limited shelf life, expiry date on the label
technique(s)
HPLC: suitable, gas chromatography (GC): suitable
mp
215 °C
application(s)
agriculture
environmental
format
neat
SMILES string
N.CP(O)(=O)CCC(N)C(O)=O
InChI
1S/C5H12NO4P.H3N/c1-11(9,10)3-2-4(6)5(7)8;/h4H,2-3,6H2,1H3,(H,7,8)(H,9,10);1H3
InChI key
ZBMRKNMTMPPMMK-UHFFFAOYSA-N
General description
Glufosinate-ammonium is a phosphinic acid analog of glutamic acid.
Application
Glufosinate-ammonium may be used as a reference standard for the determination of the analyte in:
- Human serum samples by mixed-mode solid-phase extraction (SPE), tert-butyldimethylsilyl (t-BDMS) derivatization and gas chromatography-mass spectrometry (GC-MS) operating on electron impact (EI) mode of detection.
- Water samples by ion-exchange cleanup and derivatization followed by analysis using GC coupled to tandem mass spectrometry (MS/MS) equipped with EI mode of detection.
- Finnish arable soils by high performance liquid chromatography combined with fluorescence detection (HPLC-FLD).
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Legal Information
PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany
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Danger
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Repr. 1B - STOT RE 2
Storage Class
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
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Anna R Snapp et al.
Planta, 240(3), 599-610 (2014-07-16)
Co-expression of a lesquerella fatty acid elongase and the castor fatty acid hydroxylase in camelina results in higher hydroxy fatty acid containing seeds with normal oil content and viability. Producing hydroxy fatty acids (HFA) in oilseed crops has been a
Paola M Peltzer et al.
Ecotoxicology (London, England), 22(7), 1165-1173 (2013-07-23)
In this study, amphibian tadpoles of Hypsiboas pulchellus were exposed to herbicide Liberty®, which contains glufosinate ammonium (GLA), for 48 h to the following concentrations: 0 (control), 3.55, 4.74, 6.32, 8.43, 11.25, 15, 20, 26.6, and 35.5 mg GLA L(-1).
Griet Den Herder et al.
Plant physiology, 148(1), 369-382 (2008-07-05)
Protein ubiquitination is a posttranslational regulatory process essential for plant growth and interaction with the environment. E3 ligases, to which the seven in absentia (SINA) proteins belong, determine the specificity by selecting the target proteins for ubiquitination. SINA proteins are

