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PHL80440

Ergocristine

phyproof® Reference Substance

Synonyme(s) :

12′-Hydroxy-2′-(1-methylethyl)-5′-(phenylmethyl)ergotaman-3′,6′,18′-trione

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About This Item

Formule empirique (notation de Hill):
C35H39N5O5
Numéro CAS:
511-08-0
Poids moléculaire :
609.71
Numéro CE :
208-120-7
Numéro MDL:
MFCD00215848
Code UNSPSC :
41116107
Nomenclature NACRES :
NA.24

Qualité

primary reference standard

Gamme de produits

phyproof® Reference Substance

Pureté

≥95.0% (HPLC)

Fabricant/nom de marque

PhytoLab

Pf

155-157 °C (lit.)

Application(s)

food and beverages

Format

neat

Chaîne SMILES 

CC(C)[C@@]5(NC(=O)[C@H]1CN(C)[C@@H]2Cc3c[nH]c4cccc(C2=C1)c34)O[C@@]6(O)[C@@H]7CCCN7C(=O)[C@H](Cc8ccccc8)N6C5=O

InChI

1S/C35H39N5O5/c1-20(2)34(37-31(41)23-16-25-24-11-7-12-26-30(24)22(18-36-26)17-27(25)38(3)19-23)33(43)40-28(15-21-9-5-4-6-10-21)32(42)39-14-8-13-29(39)35(40,44)45-34/h4-7,9-12,16,18,20,23,27-29,36,44H,8,13-15,17,19H2,1-3H3,(H,37,41)/t23-,27-,28+,29+,34-,35+/m1/s1

Clé InChI

HEFIYUQVAZFDEE-MKTPKCENSA-N

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Description générale

This substance is a primary reference substance with assigned absolute purity (considering chromatographic purity, water, residual solvents, inorganic impurities). The exact value can be found on the certificate. Produced by PhytoLab GmbH & Co. KG

Informations légales

phyproof is a registered trademark of PhytoLab GmbH & Co. KG

Pictogrammes

Skull and crossbones
GHS06

Mention d'avertissement

Danger

Mentions de danger

H301 + H331

Classification des risques

Acute Tox. 3 Inhalation - Acute Tox. 3 Oral

Code de la classe de stockage

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

Classe de danger pour l'eau (WGK)

WGK 3

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Certificats d'analyse (COA)

Lot/Batch Number
80951
134564725
62688890

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Navneet Kaur et al.
Journal of economic entomology, 113(5), 2079-2085 (2020-07-12)
Our previous study provided correlative evidence that morning glory species harboring endophytic fungi (Periglandula) are resistant to potato psyllid [Bactericera cockerelli (Šulc)], whereas species free of fungi often allowed psyllid development. In this study, we manipulated levels of ergot alkaloids
Céline Peillod et al.
Toxins, 13(2) (2021-03-07)
Toxic effects among fumonisins B (FB), deoxynivalenol (DON) and zearalenone (ZEN) administered alone and combined were investigated in 84-day-old ducks during force-feeding. 75 male ducks, divided into five groups of 15 animals, received daily during the meal a capsule containing
D Tardieu et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 148, 111968-111968 (2021-01-11)
Previous studies using zearalenone (ZEN) and fumonisins (FB) revealed alpha-zearalanol (α-ZOL) and FB1 in the liver of turkeys and chickens with no sign of toxicity. The aim of the present study was to determine whether contamination persists after distribution of
Angélique Travel et al.
Avian diseases, 63(4), 703-712 (2019-12-24)
Surveys of mycotoxins worldwide have shown that deoxynivalenol (DON), fumonisins (FB), and zearalenone (ZON) are the most abundant Fusarium mycotoxins (FUS) in European poultry feed, in both the level and the frequency of contamination. Previous studies reported that a combination

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