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Supelco

Glufosinate-ammonium

PESTANAL®, analytical standard

Sinonimo/i:

2-Amino-4-(hydroxymethylphosphinyl)butyric acid ammonium salt, DL-Phosphinothricin

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About This Item

Formula empirica (notazione di Hill):
C5H15N2O4P
Numero CAS:
77182-82-2
Peso molecolare:
198.16
Beilstein:
8163399
Numero CE:
278-636-5
Numero MDL:
MFCD00055562
Codice UNSPSC:
41116107
eCl@ss:
39110524
ID PubChem:
329756807
NACRES:
NA.24

Grado

analytical standard

Livello qualitativo

100

Nome Commerciale

PESTANAL®

Durata

limited shelf life, expiry date on the label

tecniche

HPLC: suitable
gas chromatography (GC): suitable

Punto di fusione

215 °C

applicazioni

agriculture
environmental

Formato

neat

Stringa SMILE

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
ZBMRKNMTMPPMMK-UHFFFAOYSA-N

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Categorie correlate

Descrizione generale

Glufosinate-ammonium is a phosphinic acid analog of glutamic acid.

Applicazioni

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.

Note legali

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

Pittogrammi

Health hazardExclamation mark
GHS08,GHS07

Avvertenze

Danger

Indicazioni di pericolo

H302 + H312 + H332,H360Fd,H373

Classi di pericolo

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Repr. 1B - STOT RE 2

Codice della classe di stoccaggio

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

Choose from one of the most recent versions:

Certificati d'analisi (COA)

Lot/Batch Number
BCCL3906
BCCG6668
BCCD1440
BCBZ5145
BCBT2199

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Sigma-Aldrich

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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
Determination of glufosinate ammonium and its metabolite, 3-methylphosphinicopropionic acid, in human serum by gas chromatography-mass spectrometry following mixed-mode solid-phase extraction and t-BDMS derivatization.
Hori Y, et al.
Journal of Analytical Toxicology, 25(8), 680-684 (2001)
Ji-Hui Byeon et al.
Biochemical and biophysical research communications, 441(1), 243-248 (2013-10-22)
We present an efficient method for the production of N-acetyl-L-phosphinothricin (N-AcPt) from commercial DL-phosphinothricin (DL-PPT) by organic acetylation for use as a negative selection agent (NSA) that induces cell death in argE transgenic rice. DL-PPT was efficiently converted into N-AcPt
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