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Category: natural substances and extractives
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 |
| Specific Gravity: | 1.05400 to 1.05900 @ 20.00 °C.
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| Pounds per Gallon - (est).: | 8.781 to 8.822
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| Refractive Index: | 1.57600 to 1.58200 @ 20.00 °C.
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| Melting Point: | 12.50 °C. @ 760.00 mm Hg
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| Boiling Point: | 277.00 °C. @ 760.00 mm Hg
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| Boiling Point: | 266.00 to 267.00 °C. @ 760.00 mm Hg (est)
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| Vapor Pressure: | 0.008000 mmHg @ 25.00 °C. (est) |
| Flash Point: | 257.00 °F. TCC ( 125.00 °C. )
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| logP (o/w): | 2.570 (est) |
| Soluble in: |
| | alcohol | | | water, 3017 mg/L @ 25 °C (est) |
| Insoluble in: |
| | water |
Organoleptic Properties:
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| Flavor Type: green |
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| | green astringent |
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| Odor and/or flavor descriptions from others (if found). |
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Cosmetic Information:
Suppliers:
Safety Information:
| Preferred SDS: View |
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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: |
subcutaneous-mouse LD50 1500 mg/kg BEHAVIORAL: TREMOR
CARDIAC: PULSE RATE INCREASE WITHOUT FALL IN BP
BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD Naunyn-Schmiedeberg's Archiv fuer Experimentelle Pathologie und Pharmakologie. Vol. 227, Pg. 129, 1955.
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| Inhalation Toxicity: |
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Not determined
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Safety in Use Information:
| Category: | natural substances and extractives |
| Recommendation for 2-benzyl pyridine usage levels up to: | | | not for fragrance use.
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| Recommendation for 2-benzyl pyridine 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- | benzylpyridine | | 2-( | phenylmethyl)pyridine | | | pyridine, 2-(phenylmethyl)- | | | pyridine, 2-benzyl- |
Articles:
| US Patents: | 3,931,166 - Certain 2,5-dimethyl-3-thiopyrazines |
| PubMed: | Spectroscopic (FTIR, FT-Raman, UV and NMR) investigation and NLO, HOMO-LUMO, NBO analysis of 2-Benzylpyridine based on quantum chemical calculations. |
| US Patents: | Flavoring agent |
| PubMed: | Copper-catalyzed α-methylenation of benzylpyridines using dimethylacetamide as one-carbon source. |
| PubMed: | Ruthenium(II) complexes of 2-benzoylpyridine-derived thiosemicarbazones with cytotoxic activity against human tumor cell lines. |
| PubMed: | Interaction between tetramethylcucurbit[6]uril and some pyridine derivates. |
| PubMed: | Synthesis, characterization, and preliminary oxygenation studies of benzyl- and ethyl-substituted pyridine ligands of carboxylate-rich diiron(II) complexes. |
| PubMed: | Oxidation of sulfide, phosphine, and benzyl substrates tethered to N-donor pyridine ligands in carboxylate-bridged diiron(II) complexes. |
| PubMed: | Reactions of an amphoteric terminal tungsten methylidyne complex. |
| PubMed: | Induction of hepatic microsomal cytochrome P450 and drug-metabolizing enzymes by 4-benzylpyridine and its structurally related compounds in rats. Dose- and sex-related differential induction of cytochrome P450 species. |
| PubMed: | Drug metabolizing enzyme induction by simple diaryl pyridines; 2-substituted isomers selectively increase only conjugation enzyme activities, 4-substituted isomers also induce cytochrome P450. |
| PubMed: | alpha-(2-Pyridine)benzyl aryl ketones as potential hypocholesteremic agents. |
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