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Safety Information

377066

Sigma-Aldrich

9,10-Dihydrolysergol

97%

Synonym(s):

6-Methylergoline-8β-methanol

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About This Item

Empirical Formula (Hill Notation):
C16H20N2O
CAS Number:
18051-16-6
Molecular Weight:
256.34
MDL number:
MFCD00134437
UNSPSC Code:
12352103

Assay

97%

SMILES string

CN1C[C@H](CO)C[C@H]2[C@H]1Cc3c[nH]c4cccc2c34

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Precautionary Statements

P261 - P305 + P351 + P338

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

377066-250MG:
377066-VAR:
377066-BULK:
377066-1G:

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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[Synthesis of glycosides and sugar orthoesters of 9,10-dihydrolysergol].
K Seifert et al.
Archiv der Pharmazie, 317(7), 577-583 (1984-07-01)
H H Pertz et al.
Journal of medicinal chemistry, 42(4), 659-668 (1999-03-03)
Three series of cycloalkanecarboxylic esters derived from the naturally occurring clavine alkaloids lysergol, dihydrolysergol-I, and elymoclavine were synthesized to study their interaction with 5-HT2A receptors and alpha1-adrenoceptors in rat tail artery and aorta, respectively. Especially cycloalkanecarboxylic esters derived from lysergol
H Pertz et al.
Naunyn-Schmiedeberg's archives of pharmacology, 345(4), 394-401 (1992-04-01)
Twelve ergolines (O-acylated lysergol and dihydrolysergol-I derivatives) were synthesized to study their antagonism of 5-HT responses in comparison with methylsergide and LY 53857 [6-methyl-1-(1-methylethyl)-8 beta-ergoline carboxylic acid 2-hydroxy-1-methylpropyl-ester hydrogen maleate] in cylindrical segments of the isolated rat tail artery. With

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