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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 |
| Melting Point: | 157.00 to 159.00 °C. @ 760.00 mm Hg
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| Boiling Point: | 160.00 to 162.00 °C. @ 760.00 mm Hg
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| Vapor Pressure: | 4.931000 mmHg @ 25.00 °C. (est) |
| Flash Point: | 90.00 °F. TCC ( 32.40 °C. ) (est)
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| logP (o/w): | 4.431 (est) |
| Soluble in: |
| | alcohol | | | water, 4.409 mg/L @ 25 °C (est) |
| Insoluble in: |
| | water |
Organoleptic Properties:
| Odor Description:mild borneol |
| Odor and/or flavor descriptions from others (if found). |
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: | | natural substances and extractives |
| Recommendation for camphane usage levels up to: | | | not for fragrance use.
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| Recommendation for camphane 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:
| | bornane | | | bornylane | | 1,7,7- | trimethyl bicyclo(2.2.1)heptane | | 1,7,7- | trimethylbicyclo[2.2.1]heptane | | 4,7,7- | trimethylbicyclo[2.2.1]heptane |
Articles:
| PubMed:Antibacterial Adhesion of Borneol-Based Polymer via Surface Chiral Stereochemistry. |
| PubMed:Design of novel camphane-based derivatives with antimycobacterial activity. |
| PubMed:Antimycobacterial activity of chiral aminoalcohols with camphane scaffold. |
| PubMed:Synthesis and antimycobacterial activity of novel camphane-based agents. |
| PubMed:Novel camphane-based anti-tuberculosis agents with nanomolar activity. |
| PubMed:Oxygen activation by P450(cin): Protein and substrate mutagenesis. |
| PubMed:GC-MS analysis of the essential oils of ripe fruits, roots and flowering aerial parts of Elaeoselinum asclepium subsp. meoides growing in Sicily. |
| PubMed:Exploring a pocket for polycycloaliphatic groups in the CXCR3 receptor with the aid of a modular synthetic strategy. |
| PubMed:Composition, enantiomeric distribution, and antibacterial activity of the essential oil of Achillea ligustica All. from Corsica. |
| PubMed:Calocedimers A, B, C, and D from the bark of Calocedrus macrolepis var. formosana. |
| PubMed:Cytochrome P450cam-monoterpene interactions. |
| PubMed:Substrates modulate the rate-determining step for CO binding in cytochrome P450cam (CYP101). A high-pressure stopped-flow study. |
| PubMed:Toxaphenes and chlorinated naphthalenes in adipose tissue of children. |
| PubMed:Changes in secondary structure and salt links of cytochrome P-450cam induced by photoreduction: a Fourier transform infrared spectroscopic study. |
| PubMed:Monoterpene synthases from common sage (Salvia officinalis). cDNA isolation, characterization, and functional expression of (+)-sabinene synthase, 1,8-cineole synthase, and (+)-bornyl diphosphate synthase. |
| PubMed:Step-scan time-resolved FTIR spectroscopy of cytochrome P-450cam carbon monoxide complex: a salt link involved in the ligand-rebinding process. |
| PubMed:Mobility of norbornane-type substrates and water accessibility in cytochrome P-450cam. |
| PubMed:Substrate mobility in thiocamphor-bound cytochrome P450cam: an explanation of the conflict between the observed product profile and the X-ray structure. |
| PubMed:Crystal structures of cytochrome P-450CAM complexed with camphane, thiocamphor, and adamantane: factors controlling P-450 substrate hydroxylation. |
| PubMed:Biosynthesis of monoterpenes: stereochemistry of the coupled isomerization and cyclization of geranyl pyrophosphate to camphane and isocamphane monoterpenes. |
| PubMed:The roles of active site hydrogen bonding in cytochrome P-450cam as revealed by site-directed mutagenesis. |
| PubMed:Metabolism of camphanediols. |
| PubMed:The influence of some new nor-camphane derivatives on the coronary flow. |
| PubMed:Metabolism of camphors and related compounds. |
| PubMed:Camphane derivatives. VII. Syntheses and structure of 3-methyl-3a-beta, 7a-beta-beta-bornano[3,2-d]oxazolidin-2-one and its derivatives. |
| PubMed:[SYNTHESES OF ANALGESICS. XXXV. CAMPHANE DERIVATIVES. (6). SYNTHESES OF CAMPHORIMIDE AND ITS DERIVATIVES]. |
| PubMed:[SYNTHESES OF ANALGESICS. XXXIV. CAMPHANE DERIVATIVES. (5). SYNTHESES OF 9- AND 10-HYDROXYCAMPHOR DERIVATIVES]. |
| PubMed:[SYNTHESES OF ANALGESICS. 33. CAMPHANE DERIVATIVES. (4). SYNTHESES OF N-(3-CAMPHORYL)-AND N-(2-HYDROXY-3-BORNANYL-AMINO ACID DERIVATES]. |
| PubMed:[SYNTHESES OF ANALGESICS. XXXII. CAMPHANE DERIVATIVES. (3). SYNTHESES OF 1-ALKYL-3-(3-CAMPHORYL)UREAS AND THIOUREAS]. |
| PubMed:[Modification of work and learning ability in rats and pigeons by 2-ethylamino-3-phenylnor-camphane]. |
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3D/inchi