dodemorph

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morpholine, 4-cyclododecyl-2,6-dimethyl-

CAS: 1593-77-7 C18 H35 N O MW: 281.48315000
All Ingredients Aromatic Ingredients CAS Numbers EINECS Numbers

Identification

Namedodemorph
IUPAC4-cyclododecyl-2,6-dimethylmorpholine
CAS Number1593-77-7
EINECS216-474-9
FDA UNII22O8GR86F0
Molecular FormulaC18 H35 N O
Molecular Weight281.48315000
MDL NumberMFCD00155442
Nikkaji NumberJ9.505B
Beilstein511312

Regulatory

Physical Properties

Assay 95.00 to 100.00
Food Chemicals Codex Listed No
Melting Point 71.00 °C. @ 760.00 mm Hg
Boiling Point 372.10 °C. @ 760.00 mm Hg (est)
Flash Point 229.00 °F. TCC ( 109.70 °C. ) (est)
logP (o/w) 6.100 (est)
Soluble in water, 2.156 mg/L @ 25 °C (est)

No sensory data available

Safety Information

Oral/Parenteral Toxicityoral-rat LD50 2645 mg/kg
Dermal Toxicityskin-rat LD50 > 2000 mg/kg
Inhalation Toxicityinhalation-rat LC50 5000 mg/m3/4H

GHS Classification

['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']

Safety in Use

Categoryherbicides / pesticides
Recommendation for dodemorph usage levels up tonot for fragrance use.
Recommendation for dodemorph flavor usage levels up tonot for flavor use.

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Potential Uses

None Found

Natural Occurrence

not found in nature

Synonyms

4- cyclododecyl-2,6-dimethylmorpholin 4- cyclododecyl-2,6-dimethylmorpholine 4- cyclododecyl-2,6-dimethylmorpholine (8CI)(9CI) doazine dodemorph [BSI:ISO] meltatox morpholine, 4-cyclododecyl-2,6-dimethyl- PubMed: Fate of the fungicide dodemorph during anaerobic digestion of biological waste. PubMed: Pesticide residues in biological waste. PubMed: Two complementary bioassays for screening the estrogenic potency of xenobiotics: recombinant yeast for trout estrogen receptor and trout hepatocyte cultures. PubMed: Risk assessment of dermal exposure of greenhouse workers to pesticides after re-entry. PubMed: Gas chromatographic determination of the pesticide dodemorph for assessment of occupational exposure. PubMed: Physiological effects of fenpropimorph on wild-type Saccharomyces cerevisiae and fenpropimorph-resistant mutants.