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Category: information only not used for fragrances or flavors
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Physical Properties:
| Assay: | 95.00 to 100.00 %
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| Food Chemicals Codex Listed: | No |
| Melting Point: | 68.50 °C. @ 760.00 mm Hg
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| Boiling Point: | 263.00 °C. @ 760.00 mm Hg
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| Vapor Pressure: | 0.013000 mmHg @ 25.00 °C. (est) |
| Flash Point: | 229.00 °F. TCC ( 109.70 °C. ) (est)
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| logP (o/w): | 2.935 (est) |
| Soluble in: |
| | water, 121.2 mg/L @ 25 °C (est) |
Organoleptic Properties:
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| Odor and/or flavor descriptions from others (if found). |
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Cosmetic Information:
Suppliers:
Safety Information:
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| Hazards identification |
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| Classification of the substance or mixture |
| GHS Classification in accordance with 29 CFR 1910 (OSHA HCS) |
| None found. |
| GHS Label elements, including precautionary statements |
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| Pictogram | |
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| Hazard statement(s) |
| None found. |
| Precautionary statement(s) |
| None found. |
| Oral/Parenteral Toxicity: |
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Not determined
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| Dermal Toxicity: |
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Not determined
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| Inhalation Toxicity: |
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Not determined
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Safety in Use Information:
| Category: | information only not used for fragrances or flavors |
| Recommendation for 2,3-dimethyl quinoline usage levels up to: | | | not for fragrance use.
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| Recommendation for 2,3-dimethyl quinoline flavor usage levels up to: |
| | not for flavor use.
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Safety References:
References:
Other Information:
Potential Blenders and core components note
Potential Uses:
Occurrence (nature, food, other): note
Synonyms:
| 2,3- | dimethylquinoline | | | quinoline, 2,3-dimethyl- |
Articles:
| PubMed: | [Studies on chemical constituents from roots of Peucedanum praeruptorum II]. |
| PubMed: | Design and synthesis of novel sulfonamide-containing bradykinin hB2 receptor antagonists. 1. Synthesis and SAR of alpha,alpha-dimethylglycine sulfonamides. |
| PubMed: | Alumina-supported synthesis of antibacterial quinolines using microwaves. |
| PubMed: | Comparative metabolism and disposition of ethoxyquin in rat and mouse. II. Metabolism. |
| PubMed: | Uptake and biotransformation of 6,7-dimethylquinoline and 6,8-dimethylquinoline by rainbow trout (Salmo gairdneri). |
| PubMed: | Mutagenicity of some synthetic quinolines and quinoxalines related to IQ, MeIQ or MeIQx in Ames test. |
| PubMed: | [Antimalarial 6-aminoquinolines. XIV. 6-(4-Diethylamino-1-methylbutylamino)-4-methoxy-2-methyl- and -2,4-dimethylquinolines with variations of substituents in positions 5 and 8]. |
| PubMed: | [Potential antimalarials. 3. (6-(4-diethylamino-1-methylbutyl)aminomethyl)-5,8-dimethoxy-2,4-dimethylquinoline]. |
| PubMed: | [Antimalarial 6-aminoquinolines. XIII. 5,8-Dialkoxyderivatives of 6-(4-diethylamino-1-methylbutylamino)-2-methyl- and 6-(4-diethylamino-1-methylbutylamino)-2,4-dimethylquinoline (author's transl)]. |
| PubMed: | Studies of the biliary excretion and metabolites of the antioxidant ethoxyquin, 6-ethoxy-2,2,4-trimethyl-1,2-dihydroquinoline in the rat. |
| PubMed: | Antimalarials. 11. 2-Vinylogs of substituted 2-aryl-4-quinoline amino alcohols. |
| PubMed: | Amodiaquine analogs. Synthesis of 6-((3-(N,N-diethylamino)methyl-4-hydroxy)anilino)5,8-dimethoxy-2,4-dimethylquinoline and related compounds. |
| PubMed: | Reaction of 2, 4-lutidine 1-oxide and 2, 4-dimethylquinoline 1-oxide with acetic anhydride. |
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