Category:pharmaceuticals / chemical synthisis
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Physical Properties:
Appearance: | colorless to pale yellow clear liquid (est) |
Assay: | 95.00 to 100.00
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Food Chemicals Codex Listed: | No |
Specific Gravity: | 0.98100 @ 25.00 °C.
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Refractive Index: | 1.54300 @ 20.00 °C.
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Melting Point: | 10.00 °C. @ 760.00 mm Hg
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Boiling Point: | 185.00 °C. @ 760.00 mm Hg
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Vapor Pressure: | 0.713000 mmHg @ 25.00 °C. (est) |
Flash Point: | 140.00 °F. TCC ( 60.00 °C. )
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logP (o/w): | 1.090 |
Soluble in: |
| water, 1.328e+005 mg/L @ 25 °C (est) |
Organoleptic Properties:
Odor and/or flavor descriptions from others (if found). |
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: |
oral-mammal (species unspecified) LD50 700 mg/kg Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 39(4), Pg. 86, 1974.
intraperitoneal-mouse LD50 600 mg/kg United States Patent Document. Vol. #3816470
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Dermal Toxicity: |
Not determined
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Inhalation Toxicity: |
Not determined
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Safety in Use Information:
Category: | pharmaceuticals / chemical synthisis |
Recommendation for benzyl amine usage levels up to: | | not for fragrance use.
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Recommendation for benzyl amine 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:
( | aminomethyl)benzene | | aminomethylbenzene | p- | aminomethylbenzene | a- | aminotoluene | | benzenemethanamine | | benzydamine | | benzyl-amine | | benzylamine | mono | benzylamine | N- | benzylamine | | methylamine, 1-phenyl- | | methylphenylamine | | moringine | | phenyl-methanamine | | phenylmethanamine | 1- | phenylmethanamine | ( | phenylmethyl)amine | | sumine 2005 |
Articles:
PubMed:Biocatalytic behaviour of immobilized Rhizopus oryzae lipase in the 1,3-selective ethanolysis of sunflower oil to obtain a biofuel similar to biodiesel. |
PubMed:Macamides and their synthetic analogs: evaluation of in vitro FAAH inhibition. |
PubMed:The amine oxidase inhibitor phenelzine limits lipogenesis in adipocytes without inhibiting insulin action on glucose uptake. |
PubMed:Effects of amine oxidases in allergic and histamine-mediated conditions. |
PubMed:Oral Administration of Semicarbazide Limits Weight Gain together with Inhibition of Fat Deposition and of Primary Amine Oxidase Activity in Adipose Tissue. |
PubMed:Cerebral serotonin transporter binding is inversely related to body mass index. |
PubMed:Pharmacological and pharmacokinetic characterization of 2-piperazine-alpha-isopropyl benzylamine derivatives as melanocortin-4 receptor antagonists. |
PubMed:Isolation and structure elucidation of antioxidant polyphenols from quince (Cydonia vulgaris) peels. |
PubMed:Design, synthesis, in vitro, and in vivo characterization of phenylpiperazines and pyridinylpiperazines as potent and selective antagonists of the melanocortin-4 receptor. |
PubMed:Reduction of fat deposition by combined inhibition of monoamine oxidases and semicarbazide-sensitive amine oxidases in obese Zucker rats. |
PubMed:Controlled atmosphere treatment of broccoli after harvest delays senescence and induces the expression of novel BoCAR genes. |
PubMed:Induction by antipsychotics of "win-shift" in the drug discrimination paradigm. |
PubMed:Random chemistry as a new tool for the generation of small-compound libraries. |
PubMed:N-(2-bromophenyl)-2-(4,6-dimethoxypyrimidin-2-yloxy)benzylamine, a new selective postemergent herbicide for weed control in winter oilseed rape. |
PubMed:Amine degradation by 4,5-epoxy-2-decenal in model systems. |
PubMed:Activity and expression of semicarbazide-sensitive benzylamine oxidase in a rodent model of diabetes: interactive effects with methylamine and alpha-aminoguanidine. |
PubMed:4-methyl benzylamine stimulates food consumption and counteracts the hypophagic effects of amphetamine acting on brain Shaker-like Kv1.1 channels. |
PubMed:Oxidative deamination of benzylamine and lysine residue in bovine serum albumin by green tea, black tea, and coffee. |
PubMed:A potent and selective nonpeptide antagonist of the melanocortin-4 receptor induces food intake in satiated mice. |
PubMed:Selective herbicide activity of 2,5-di(benzylamine)-p-benzoquinone against the monocot weed Echinochloa crusgalli. An in vivo analysis of photosynthesis and growth. |
PubMed:Promoting effect and recovery activity from physical stress of the fruit of Morus alba. |
PubMed:The reduction of food intake induced in mice by benzylamine and its derivatives. |
PubMed:Intake of volatile N-nitrosamines and their ability to exogenously synthesize in the diet of inhabitants from high-risk area of esophageal cancer in southern China. |
PubMed:High-performance liquid chromatographic determination of biogenic amines in poultry carcasses. |
PubMed:Monoamine oxidase B and free radical scavenging activities of natural flavonoids in Melastoma candidum D. Don. |
PubMed:Selective inhibition of amine oxidases differently potentiate the hypophagic effect of benzylamine in mice. |
PubMed:Stereochemical course of tyramine oxidation by semicarbazide-sensitive amine oxidase. |
PubMed:The effects of Chinese tea on the occurrence of esophageal tumors induced by N-nitrosomethylbenzylamine in rats. |
PubMed:The effects of Chinese tea on the methylation of DNA by the esophageal carcinogen N-nitrosomethylbenzylamine. |
PubMed:Trapping of reactive intermediates from the nitrosation of primary amines by a new type of scavenger reagent. |
PubMed:Correlation of platelet MAO activity with introversion: a study on a German rural population. |
PubMed:Bacterial degradation of benzyl isothiocyanate. |
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toluenes in which one hydrogen of the methyl group is substituted by an amino group. permitted are any substituents on the benzene ring or the amino group. Alkaloid from Moringa oleifera (horseradish tree)
Benzylamine is the chemical compound with the formula C6H5CH2NH2. It consists of a benzyl group, C6H5CH2, attached to an amine functional group. This colorless liquid is a common precursor in organic synthesis.
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