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Safety Information

36199

Supelco

Tridemorph

PESTANAL®, analytical standard

Synonym(s):

2,6-Dimethyl-4-tridecylmorpholine

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About This Item

Empirical Formula (Hill Notation):
C19H39NO
CAS Number:
24602-86-6
Molecular Weight:
297.52
EC Number:
246-347-3
MDL number:
MFCD00055522
UNSPSC Code:
41116107
PubChem Substance ID:
329755340
NACRES:
NA.24

grade

analytical standard

Quality Level

100

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

agriculture
cleaning products
cosmetics
environmental
food and beverages
personal care

format

neat

SMILES string

CCCCCCCCCCCCCN1CC(C)OC(C)C1

InChI

1S/C19H39NO/c1-4-5-6-7-8-9-10-11-12-13-14-15-20-16-18(2)21-19(3)17-20/h18-19H,4-17H2,1-3H3

InChI key

YTOPFCCWCSOHFV-UHFFFAOYSA-N

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Application

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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Signal Word

Danger

Hazard Classifications

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Repr. 1B - Skin Irrit. 2

Storage Class Code

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

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

农药列管产品

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Certificates of Analysis (COA)

Lot/Batch Number
BCBW9105

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J P Keon et al.
Current genetics, 25(6), 531-537 (1994-06-01)
The Magnaporthe grisea ERG2 gene, encoding delta 8-->delta 7 sterol isomerase, was isolated from a genomic library by heterologous hybridization to a fragment of the Ustilago maydis ERG2 gene. The isolated gene contained a reading frame of 745 bp which
F Cortés et al.
Cytobios, 34(135-36), 181-190 (1982-01-01)
A mitodepressive effect of Tridemorph on the meristematic cells of Allium cepa has been observed. This effect increases with the concentration of the fungicide and the length of treatment, until complete inhibition of cell division occurs under certain conditions. Furthermore
J Merkle et al.
Teratology, 29(2), 259-269 (1984-04-01)
Tridemorph (N-tridecyl-2,6-dimethylmorpholine), the active ingredient of the commercially formulated fungicide Calixin, is a teratogen in rats and mice. The no-effect level for embryotoxic effects was 27.5 mg/kg for mice and 20.6 mg/kg for rats. By contrast, when Calixin, which contains
Xia Tian et al.
The Journal of organic chemistry, 71(8), 3176-3183 (2006-04-08)
Tandem Prins cyclization and Friedel-Crafts reaction with an electron-rich aromatic ring were used to prepare the core structures of calyxin natural products. The proposed structure of epicalyxin F was prepared and shown to be incorrect. Several calyxin natural products, including
S Silve et al.
Biochimica et biophysica acta, 1392(2-3), 233-244 (1998-06-19)
Lamin B receptor (LBR), a nuclear protein of avian and mammalian cells, contains an hydrophobic domain that shares extensive structural similarities with the members of the sterol reductase family. To test if the sterol-reductase-like domain of LBR could be enzymatically
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