(R)-styralyl alcohol
benzenemethanol, a-methyl-, (aR)-
 
Notes:
None found
  • BOC Sciences
    • BOC Sciences
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      Product(s):
      1517-69-7 (R)-1-phenyl-1-ethanol ≥98%, ≥95%e.e.
       
  • TCI AMERICA
    • TCI AMERICA
      Moving Your Chemistry Forward
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      Tokyo Chemical Industry Co., Ltd. (TCI) is a leading worldwide manufacturer of specialty organic chemicals founded in 1946. TCI provides organic laboratory chemicals as well as pharmaceutical, cosmetic and functional materials. More than 70 years of synthesis experience and multi-purpose plants enable TCI to offer more than 30,000 products as well as custom synthesis.
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      Product(s):
      P0795 (R)-(+)-1-Phenylethyl Alcohol >98.0%(GC)
       
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CAS Number: 1517-69-7Picture of molecule3D/inchi
FDA UNII: 36N222W94B
Nikkaji Web: J56.779E
Beilstein Number: 3648469
XlogP3: 1.40 (est)
Molecular Weight: 122.16690000
Formula: C8 H10 O
BioActivity Summary: listing
NMR Predictor: Predict (works with chrome or firefox)
Category: flavor and fragrance agents
 
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Google Scholar: Search
Google Books: Search
Google Scholar: with word "volatile"Search
Google Scholar: with word "flavor"Search
Google Scholar: with word "odor"Search
Perfumer and Flavorist: Search
Google Patents: Search
US Patents: Search
EU Patents: Search
Pubchem Patents: Search
PubMed: Search
NCBI: Search
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Physical Properties:
Appearance: colorless clear liquid (est)
Assay: 95.00 to 100.00 % 
Food Chemicals Codex Listed: No
Specific Gravity: 1.01300 to 1.01500 @  20.00 °C.
Pounds per Gallon - (est).: 8.439 to  8.456
Refractive Index: 1.52500 to 1.52900 @  20.00 °C.
Optical Rotation: +43.0 to +48.0
Melting Point: 11.00 °C. @ 760.00 mm Hg
Boiling Point: 206.00 to  207.00 °C. @ 760.00 mm Hg (est)
Vapor Pressure: 0.139000 mmHg @ 25.00 °C. (est)
Flash Point: 185.00 °F. TCC ( 85.00 °C. )
logP (o/w): 1.420
Soluble in:
 alcohol
 water, 1.954e+004 mg/L @ 25 °C (est)
 water, 1.47E+04 mg/L @ 25 °C (exp)
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Organoleptic Properties:
 
Odor Type: floral
 
Odor Strength: medium
 
 floral  earthy  green  honeysuckle  
Odor Description:
at 100.00 %. 
floral earthy green honeysuckle
 
Odor and/or flavor descriptions from others (if found).
 
 
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Cosmetic Information:
None found
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Suppliers:
BOC Sciences
For experimental / research use only.
(R)-1-phenyl-1-ethanol ≥98%, ≥95%e.e.
Carbosynth
For experimental / research use only.
(R)-1-Phenylethanol
EMD Millipore
For experimental / research use only.
(R)-(+)-1-Phenylethanol
Santa Cruz Biotechnology
For experimental / research use only.
(R)-(+)-1-Phenylethanol
Sigma-Aldrich: Aldrich
For experimental / research use only.
(R)-1-Phenylethanol 97%
Takasago
(R)-1-Phenylethanol
The Fragrance Museum
TCI AMERICA
For experimental / research use only.
(R)-(+)-1-Phenylethyl Alcohol >98.0%(GC)
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Safety Information:
Preferred SDS: View
 
Hazards identification
 
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
None found.
GHS Label elements, including precautionary statements
 
Pictogram
 
Hazard statement(s)
None found.
Precautionary statement(s)
None found.
Oral/Parenteral Toxicity:
Not determined
Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined
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Safety in Use Information:
Category: flavor and fragrance agents
IFRA Code of Practice Notification of the 49th Amendment to the IFRA Code of Practice
 
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Safety References:
EPI System: View
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 637516
National Institute of Allergy and Infectious Diseases: Data
 (1R)-1-phenylethanol
Chemidplus: 0001517697
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References:
Leffingwell: Chirality or Article
 (1R)-1-phenylethanol
NIST Chemistry WebBook: Search Inchi
Pubchem (cid): 637516
Pubchem (sid): 135051670
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Other Information:
(IUPAC): Atomic Weights of the Elements 2011 (pdf)
Videos: The Periodic Table of Videos
tgsc: Atomic Weights use for this web site
(IUPAC): Periodic Table of the Elements
CHEBI: View
CHEMBL: View
HMDB (The Human Metabolome Database): Search
Export Tariff Code: 2906.29.6000
ChemSpider: View
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Potential Blenders and core components note
 
For Odor
balsamic
 bornyl formateFL/FR
caramellic
2-isobutyl-3-methyl pyrazineFL/FR
coconut
delta-heptalactoneFL/FR
earthy
5-cyclopropyl-3(or 2),4-dimethyl octahydro-4,7-methanoinden-5-ol 
(Z)-linalool oxide (furanoid)FL/FR
1-nonen-3-olFL/FR
2-octanone oximeFR
1-octen-3-olFL/FR
fatty
(R)-dihydro-gamma-ionone 
(Z)-3-octen-1-olFL/FR
floral
 bois de rose oil terpenelessFL/FR
 citronellyl valerateFL/FR
 geranium dihydropyranFR
 geranium oil moroccoFL/FR
 linalool oxideFL/FR
 linden flower absoluteFR
2-methyl-4-phenyl butanalFL/FR
 octyl acetateFL/FR
 phenethyl alcoholFL/FR
2-phenyl propyl acetateFL/FR
 ylang ylang flower oil IIIFL/FR
fruity
 allyl phenoxyacetateFL/FR
 amyl formateFL/FR
2-pentyl furanFL/FR
green
(R)-2-sec-butyl-3-methoxypyrazine 
(S)-2-sec-butyl-3-methoxypyrazine 
 cumin acetaldehydeFL/FR
alpha,alpha-dimethyl benzyl alcoholFL/FR
 earthy acetalFL/FR
 fern absolute 
 ferula galbaniflua gum extractFL/FR
 galbanum resinoid replacerFR
 geranium absoluteFL/FR
(Z)-3-hepten-1-olFL/FR
(Z)-3-hexen-1-yl acetoacetateFL/FR
(R)-1-hexen-3-ol 
(S)-1-hexen-3-ol 
 methyl cyclocitrone (IFF)FR
 octanal dimethyl acetalFL/FR
 rose furan epoxideFL/FR
3,5,5-trimethyl hexanolFL/FR
2,4,8-trimethyl-5-oxatricyclo(6.2.1.0*2,6*)undecaneFR
1,5-undecadien-4-ol 
6-hydroxydihydrotheaspirane (mixture of isomers)FL/FR
naphthyl
ortho-methyl anisoleFL/FR
nutty
5-ethyl-4-methyl thiazole 
woody
3(or 2),4-dimethyl-5-vinyl octahydro-4,7-methanoinden-5-ol 
 dryopteris filix-mas oleoresinFR
5,5a,6,7,8,8a-hexahydro-6,6,7,8,8-pentamethyl-4H-indeno[5,4-D]isoxazole 
 
For Flavor
 
No flavor group found for these
 benzyl disulfideFL
 bornyl formateFL/FR
(S)-2-sec-butyl-3-methoxypyrazine 
(R)-2-sec-butyl-3-methoxypyrazine 
 citronellyl valerateFL/FR
5-cyclopropyl-3(or 2),4-dimethyl octahydro-4,7-methanoinden-5-ol 
(R)-dihydro-gamma-ionone 
alpha,alpha-dimethyl benzyl alcoholFL/FR
3(or 2),4-dimethyl-5-vinyl octahydro-4,7-methanoinden-5-ol 
 earthy acetalFL/FR
5-ethyl-4-methyl thiazole 
 fern absolute 
 fig leaf absoluteFL
(Z)-3-hepten-1-olFL/FR
5,5a,6,7,8,8a-hexahydro-6,6,7,8,8-pentamethyl-4H-indeno[5,4-D]isoxazole 
(Z)-3-hexen-1-yl acetoacetateFL/FR
(S)-1-hexen-3-ol 
(R)-1-hexen-3-ol 
(Z)-linalool oxide (furanoid)FL/FR
2-methyl-4-phenyl butanalFL/FR
2-phenyl propyl acetateFL/FR
 rose furan epoxideFL/FR
1,5-undecadien-4-ol 
camphoreous
6-hydroxydihydrotheaspirane (mixture of isomers)FL/FR
ortho-methyl anisoleFL/FR
earthy
1-nonen-3-olFL/FR
fatty
(Z)-3-octen-1-olFL/FR
floral
 bois de rose oil terpenelessFL/FR
 geranium oil moroccoFL/FR
 phenethyl alcoholFL/FR
 ylang ylang flower oil IIIFL/FR
fruity
 allyl phenoxyacetateFL/FR
 amyl formateFL/FR
green
2-isobutyl-3-methyl pyrazineFL/FR
 cumin acetaldehydeFL/FR
 ferula galbaniflua gum extractFL/FR
 geranium absoluteFL/FR
 horseradish oilFL
 linalool oxideFL/FR
 octanal dimethyl acetalFL/FR
2-pentyl furanFL/FR
 propylene glycol acetone ketalFL
3,5,5-trimethyl hexanolFL/FR
lactonic
delta-heptalactoneFL/FR
mushroom
1-octen-3-olFL/FR
waxy
 octyl acetateFL/FR
 
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Potential Uses:
None Found
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Occurrence (nature, food, other): note
 not found in nature
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Synonyms:
 benzenemethanol, a-methyl-, (aR)-
 benzenemethanol, a-methyl-, (R)-
(R)-alpha-methyl benzyl alcohol
(R)-a-methylbenzenemethanol
(R)-a-methylbenzyl alcohol
(R)-(+)-sec-phenethyl alcohol
(1R)-1-phenylethan-1-ol
(1R)-1-phenylethanol
(R)-(+)-1-phenylethanol
(R)-1-phenylethanol
(R)-(+)-1-phenylethyl alcohol
(R)-styrallyl alcohol
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