4-phenyl-2-butanol
4-phenylbutan-2-ol
 
Notes:
Used as a food additive [EAFUS]
  • Alfrebro
    • Alfrebro LLC/ Archer Daniels Midland Company
      Let's get reacquainted
      Building great taste with aroma chemicals, extracts, and distillates
      The Alfrebro brand was established in the early 1900s by Alex Fries & Brothers, a Cincinnati Flavor Company. In 1980, the brand was re-launched as an aroma chemical manufacturer. Since its inception, Alfrebro’s primary focus has been to provide quality natural and high value synthetic chemicals.
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      Product(s):
      4-PHENYL-2-BUTANOL NATURAL
       
  • BOC Sciences
    • BOC Sciences
      Best of Chemicals Supplier
      Quality supplier of research chemicals and biochemicals including inhibitors, building blocks, GMP Products, impurities and metabolites, APIs for Veterinary, Natural Compounds, ADCs, Stem Cell Molecule and chiral compounds.
      BOC Sciences provides a wide range of services to support the pharmaceutical industry through all stages of drug discovery including Custom Synthesis of those chemicals that are not in stock, Isotope Labeling Service, Chiral Synthesis and Resolution, Bioconjugation, PEGylation services, analytical services.
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      Product(s):
      2344-70-9 4-Phenyl-2-butanol
       
  • Penta International
    • Penta International Corporation
      Chemistry innovation
      At Penta, our products and services help businesses do business better.
      For over 30 years, Penta Manufacturing Company has played a growing role in worldwide chemistry innovations and applications. As an industry leader, Penta continues to pioneer chemistry-based solutions for practically every area of commerce. Our products and expertise have helped fuel technical advances in dozens of commercial applications including flavoring, coloring, fragrances and chemical processes.
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      Product(s):
      16-25000 4-PHENYL-2-BUTANOL
       
  • Synerzine
    • Synerzine, Inc.
      Innovation. Customization. Aroma Ingredients.
      Synerzine is a leading supplier of flavor and fragrance ingredients.
      Synerzine expresses what we have grown to embody as an organization - the synergy and connection between raw ingredients, science, technology, and the final product. Our experienced team is passionate about bringing our customers high-quality innovative ingredients that they can trust.
      Building upon our 44 year history, the Synerzine team provides customers around the globe with convenient access to over 1200 high-quality aroma ingredients. We actively engage with customers to add a wide array of new products and services on a regular basis. Our aim is to delight every customer with our exceptional services, large product selection, customization and the highest quality and safety standards. We provide our customers with true value designed to help them bring their products to market faster.
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      Product(s):
      W1705 4-Phenyl-2-butanol
       
  • TCI AMERICA
    • TCI AMERICA
      Moving Your Chemistry Forward
      We continuously strive to advance our technology.
      With East & West Coast distribution centers, count on TCI to deliver products quickly and reliably. Over 30,000 Reagents available today in benchtop to bulk quantities. We also offer custom synthesis solutions. Sign up for a TCI account today for fast and free shipping!
      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):
      P0876 4-Phenyl-2-butanol >99.0%(GC)
       
Synonyms   Articles   Notes   Search
CAS Number: 2344-70-9Picture of molecule3D/inchi
ECHA EINECS - REACH Pre-Reg: 219-055-9
FDA UNII: SZ2IE5UDQR
Nikkaji Web: J1.806F
MDL: MFCD00044349
CoE Number: 85
XlogP3-AA: 2.30 (est)
Molecular Weight: 150.22078000
Formula: C10 H14 O
BioActivity Summary: listing
NMR Predictor: Predict (works with chrome, Edge 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
JECFA Food Flavoring: 815  4-phenyl-2-butanol
DG SANTE Food Flavourings: 02.036  4-phenylbutan-2-ol
FEMA Number: 2879 4-phenyl-2-butanol
FDA:No longer provide for the use of these seven synthetic flavoring substances
FDA Mainterm (SATF):2344-70-9 ; 4-PHENYL-2-BUTANOL
FDA Regulation:
FDA PART 172 -- FOOD ADDITIVES PERMITTED FOR DIRECT ADDITION TO FOOD FOR HUMAN CONSUMPTION
Subpart F--Flavoring Agents and Related Substances
Sec. 172.515 Synthetic flavoring substances and adjuvants.
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Physical Properties:
Appearance: colorless clear oily liquid (est)
Assay: 97.00 to 100.00 % 
Additional Assay Information: racemate
Food Chemicals Codex Listed: No
Specific Gravity: 0.97700 to 0.98300 @  25.00 °C.
Pounds per Gallon - (est).: 8.130 to  8.180
Refractive Index: 1.51400 to 1.51800 @  20.00 °C.
Boiling Point: 123.00 to  124.00 °C. @ 15.00 mm Hg
Boiling Point: 239.00 to  240.00 °C. @ 760.00 mm Hg
Vapor Pressure: 0.015000 mmHg @ 25.00 °C. (est)
Flash Point: 231.00 °F. TCC ( 110.56 °C. )
logP (o/w): 2.131 (est)
Soluble in:
 alcohol
 water, 1885 mg/L @ 25 °C (est)
Insoluble in:
 water
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Organoleptic Properties:
 
Odor Type: floral
 
Odor Strength: medium
 
Substantivity: 44 hour(s) at 100.00 %
 
 floral  peony  foliage  sweet  mimosa  heliotrope  
Odor Description:
at 100.00 %. 
floral peony foliage sweet mimosa heliotrope
Luebke, William tgsc, (2007)
 
 
Flavor Type: floral
 
 floral  spicy  magnolia  mango  green  petal  tropical  melon  
Taste Description:
floral spicy magnolia mango green petal tropical melon
Luebke, William tgsc, (2007)
 
Odor and/or flavor descriptions from others (if found).
 
 
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Cosmetic Information:
None found
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Suppliers:
Alfrebro
4-PHENYL-2-BUTANOL NATURAL
Odor: Aromatic, Floral
BOC Sciences
For experimental / research use only.
4-Phenyl-2-butanol
EMD Millipore
For experimental / research use only.
4-Phenyl-2-butanol
Ernesto Ventós
4-PHENYL-2-BUTANOL
Odor: FRUITY, FLORAL
Penta International
4-PHENYL-2-BUTANOL
Reincke & Fichtner
4-Phenyl-2-butanol
Santa Cruz Biotechnology
For experimental / research use only.
4-Phenyl-2-butanol ≥98%
Sigma-Aldrich: Aldrich
For experimental / research use only.
4-Phenyl-2-butanol 97%
Synerzine
4-Phenyl-2-butanol
TCI AMERICA
For experimental / research use only.
4-Phenyl-2-butanol >99.0%(GC)
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Safety Information:
Preferred SDS: View
European information :
Most important hazard(s):
None - None found.
S 02 - Keep out of the reach of children.
S 24/25 - Avoid contact with skin and eyes.
 
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
RIFM Fragrance Material Safety Assessment: Search
IFRA Code of Practice Notification of the 49th Amendment to the IFRA Code of Practice
Recommendation for 4-phenyl-2-butanol usage levels up to:
  8.0000 % in the fragrance concentrate.
 
Maximised Survey-derived Daily Intakes (MSDI-EU): 1.20 (μg/capita/day)
Maximised Survey-derived Daily Intakes (MSDI-USA): 0.30 (μg/capita/day)
Threshold of Concern:1800 (μg/person/day)
Structure Class: I
Use levels for FEMA GRAS flavoring substances on which the FEMA Expert Panel based its judgments that the substances are generally recognized as safe (GRAS).
The Expert Panel also publishes separate extensive reviews of scientific information on all FEMA GRAS flavoring substances and can be found at FEMA Flavor Ingredient Library
publication number: 3
Click here to view publication 3
 average usual ppmaverage maximum ppm
baked goods: 1.5000015.00000
beverages(nonalcoholic): 0.120000.90000
beverages(alcoholic): --
breakfast cereal: --
cheese: --
chewing gum: --
condiments / relishes: --
confectionery froastings: --
egg products: --
fats / oils: --
fish products: --
frozen dairy: 0.600006.00000
fruit ices: 0.600006.00000
gelatins / puddings: --
granulated sugar: --
gravies: --
hard candy: 1.5000015.00000
imitation dairy: --
instant coffee / tea: --
jams / jellies: --
meat products: --
milk products: --
nut products: --
other grains: --
poultry: --
processed fruits: --
processed vegetables: --
reconstituted vegetables: --
seasonings / flavors: --
snack foods: --
soft candy: --
soups: --
sugar substitutes: --
sweet sauces: --
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Safety References:
Flavor & Extract Manufacturers Association (FEMA) reference(s):
The FEMA GRAS assessment of aromatic substituted secondary alcohols, ketones, and related esters used as flavor ingredients. View pdf
European Food Safety Athority(EFSA): Flavor usage levels; Subacute, Subchronic, Chronic and Carcinogenicity Studies; Developmental / Reproductive Toxicity Studies; Genotoxicity Studies...
European Food Safety Authority (EFSA) reference(s):
Opinion of the Scientific Panel on food additives, flavourings, processing aids and materials in contact with food (AFC) related to Flavouring Group Evaluation 16 (FGE.16): Aromatic ketones from chemical group 21 (Commission Regulation (EC) No 1565/2000 of 18 July 2000)
View page or View pdf
Flavouring Group Evaluation 16, Revision 1 (FGE.16Rev1)[1]: Aromatic ketones from chemical group 21- Opinion of the Scientific Panel on Food Additives, Flavourings, Processing Aids and Materials in Contact with Food
View page or View pdf
Flavouring Group Evaluation 69, (FGE.69)[1] - Consideration of aromatic substituted secondary alcohols, ketones and related esters evaluated by JECFA (57th meeting) structurally related to aromatic ketones from chemical group 21 evaluated by EFSA in FGE.16 (2006) - Opinion of the Scientific Panel on Food Additives, Flavourings, Processing Aids and Materials in Contact with Food
View page or View pdf
Flavouring Group Evaluation 16, Revision 2 (FGE.16Rev2): Aromatic ketones from chemical group 21
View page or View pdf
Scientific Opinion on Flavouring Group Evaluation 69, Revision 1 (FGE.69Rev1): consideration of aromatic substituted secondary alcohols, ketones and related esters evaluated by JECFA (57th meeting), structurally related to aromatic ketones from chemical group 21 evaluated by EFSA in FGE.16Rev2
View page or View pdf
EPI System: View
AIDS Citations: Search
Cancer Citations: Search
Toxicology Citations: Search
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 61302
National Institute of Allergy and Infectious Diseases: Data
WGK Germany: 3
 4-phenylbutan-2-ol
Chemidplus: 0002344709
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References:
 4-phenylbutan-2-ol
NIST Chemistry WebBook: Search Inchi
Canada Domestic Sub. List: 2344-70-9
Pubchem (cid): 61302
Pubchem (sid): 135017447
Pherobase: View
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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
FDA Substances Added to Food (formerly EAFUS): View
HMDB (The Human Metabolome Database): HMDB31613
FooDB: FDB008249
Export Tariff Code: 2906.29.6000
VCF-Online: VCF Volatile Compounds in Food
ChemSpider: View
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Potential Blenders and core components note
 
For Odor
aldehydic
aldehydic
 muguet undecadienalFR
anisic
para-anisaldehydeFL/FR
balsamic
 benzyl cinnamateFL/FR
 cinnamyl alcoholFL/FR
 cinnamyl formateFL/FR
 phenethyl cinnamateFL/FR
2-phenyl propyl alcoholFL/FR
citrus
 grapefruit pentanolFR
 heptyl phenyl acetate 
 lemongrass oilFL/FR
fatty
2-decenalFL/FR
5-methyl-5-hexen-2-oneFL/FR
floral
 acetophenoneFL/FR
 amyl benzoateFL/FR
para-anisaldehyde / methyl anthranilate schiff's baseFR
 anisyl propanal / methyl anthranilate schiff's baseFR
alpha-butyl cinnamaldehydeFL/FR
 citronellyl acetateFL/FR
 citronellyl propionateFL/FR
para-cresyl propionaldehydeCS
 cumin carbinolFR
2',4'-dimethyl acetophenoneFL/FR
 dimethyl benzyl carbinolFL/FR
 dimethyl benzyl carbinyl butyrateFL/FR
6,8-dimethyl-2-nonanolFR
 floral butanalFR
 geranium oil africaFL/FR
 geranium oil bourbonFL/FR
 geranium oil chinaFL/FR
 geranyl acetoneFL/FR
 geranyl isobutyrateFL/FR
 hawthorn carbinolFL/FR
 heliotrope absoluteFR
 heliotropinFL/FR
 heliotropyl acetoneFL/FR
(Z)-3-hexen-1-yl salicylateFL/FR
alpha-hexyl cinnamaldehydeFL/FR
 ho leaf oilFR
 jasmin cyclopentanolFR
isojasmoneFL/FR
 jonquil absoluteFR
para-methyl acetophenoneFL/FR
 mimosa absolute franceFL/FR
 mimosa heptanalFR
 neroli oil bigardeFL/FR
 nerolidolFL/FR
(Z)-beta-ocimeneFL/FR
 orange leaf absoluteFL/FR
 papaya isobutyrateFL/FR
2-pentadecanoneFL/FR
 peony alcoholFR
2-phenyl propionaldehyde dimethyl acetalFL/FR
2-phenyl propionaldehyde ethylene glycol acetalFR
(R)-2-phenyl propyl alcoholFL/FR
3-phenyl propyl propionateFL/FR
 rose absolute (rosa centifolia) moroccoFL/FR
 rose butanoateFL/FR
 rose oil (rosa centifolia) egyptFL/FR
 rose oil (rosa damascena) iranFL/FR
 rose petal acetateFR
 styralyl formateFL/FR
 sweet pea absoluteFR
 tuberose absolute (from pommade)FL/FR
 tuberose absolute chassisFL/FR
 verdyl acetateFR
fruity
 ethyl methyl-para-tolyl glycidateFL/FR
 prenyl acetateFL/FR
green
homocuminic aldehydeFR
 galbanum resinoidFL/FR
(Z)-3-hexen-1-olFL/FR
alpha-hexyl cinnamaldehyde dimethyl acetalFR
 hexyl heptanoateFL/FR
 hexyl phenyl acetateFL/FR
 hyacinth absoluteFL/FR
 hyacinth butanalFR
 ivy dioxolaneFR
english ivy leaf absoluteFR
 marigold pot absoluteFL/FR
para-methyl hydratropaldehydeFL/FR
 methyl octine carbonateFL/FR
2-nonyn-1-al dimethyl acetalFR
 octanal dimethyl acetalFL/FR
 phenethyl isopropyl etherFR
 phenyl acetaldehyde dimethyl acetalFL/FR
3-phenyl propionaldehydeFL/FR
herbal
 anthemis nobilis flower oil romanFL/FR
 clary sage absoluteFL/FR
 mistletoe absolute 
alpha-terpinyl acetateFL/FR
licorice
(E)-anetholFL/FR
spicy
 cardamom seed oil CO2 extractFL/FR
 cinnamyl acetateFL/FR
sulfurous
 methyl 3-(methyl thio) propionateFL/FR
vanilla
 vanillyl acetateFL/FR
waxy
3-decanoneFL/FR
 
For Flavor
 
No flavor group found for these
 amyl benzoateFL/FR
3-decanoneFL/FR
2',4'-dimethyl acetophenoneFL/FR
 heptyl phenyl acetate 
 hexyl heptanoateFL/FR
 hyacinth absoluteFL/FR
 mistletoe absolute 
(R)-2-phenyl propyl alcoholFL/FR
3-phenyl propyl propionateFL/FR
 styralyl formateFL/FR
alpha-butyl cinnamaldehydeFL/FR
4'-hydroxyacetophenoneFL
anise
(E)-anetholFL/FR
balsamic
 phenethyl cinnamateFL/FR
berry
 heliotropyl acetoneFL/FR
cherry
 heliotropinFL/FR
citrus
 lemongrass oilFL/FR
creamy
para-anisaldehydeFL/FR
para-methyl acetophenoneFL/FR
ethereal
5-methyl-5-hexen-2-oneFL/FR
fatty
2-decenalFL/FR
2-pentadecanoneFL/FR
floral
 citronellyl acetateFL/FR
 citronellyl propionateFL/FR
 dimethyl benzyl carbinyl butyrateFL/FR
 geranium oil africaFL/FR
 geranium oil bourbonFL/FR
 geranium oil chinaFL/FR
 geranyl acetoneFL/FR
 geranyl isobutyrateFL/FR
 neroli oil bigardeFL/FR
 orange leaf absoluteFL/FR
 rose absolute (rosa centifolia) moroccoFL/FR
 rose oil (rosa centifolia) egyptFL/FR
 rose oil (rosa damascena) iranFL/FR
 tuberose absolute (from pommade)FL/FR
 tuberose absolute chassisFL/FR
fruity
 ethyl methyl-para-tolyl glycidateFL/FR
 hexyl phenyl acetateFL/FR
2-phenyl propionaldehyde dimethyl acetalFL/FR
 prenyl acetateFL/FR
 rose butanoateFL/FR
green
 cinnamyl alcoholFL/FR
 galbanum resinoidFL/FR
(Z)-3-hexen-1-olFL/FR
(Z)-3-hexen-1-yl salicylateFL/FR
isojasmoneFL/FR
 marigold pot absoluteFL/FR
para-methyl hydratropaldehydeFL/FR
 methyl octine carbonateFL/FR
 nerolidolFL/FR
(Z)-beta-ocimeneFL/FR
 octanal dimethyl acetalFL/FR
 papaya isobutyrateFL/FR
 phenyl acetaldehyde dimethyl acetalFL/FR
3-phenyl propionaldehydeFL/FR
2-phenyl propyl alcoholFL/FR
herbal
 anthemis nobilis flower oil romanFL/FR
 clary sage absoluteFL/FR
 lavender flavorFL
medicinal
 dimethyl benzyl carbinolFL/FR
powdery
 acetophenoneFL/FR
spicy
 acacia flavorFL
 benzyl cinnamateFL/FR
 cardamom seed oil CO2 extractFL/FR
 cinnamyl acetateFL/FR
 cinnamyl formateFL/FR
 hawthorn carbinolFL/FR
tropical
 guava distillatesFL
vanilla
 vanillyl acetateFL/FR
vegetable
 methyl 3-(methyl thio) propionateFL/FR
waxy
alpha-hexyl cinnamaldehydeFL/FR
 mimosa absolute franceFL/FR
woody
alpha-terpinyl acetateFL/FR
 
Synonyms   Articles   Notes   Search   Top
Potential Uses:
 floralFR
 peonyFR
 roseFR
Synonyms   Articles   Notes   Search   Top
Occurrence (nature, food, other): note
 blackberry fruit
Search  PMC Picture
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Synonyms:
 benzenepropanol, a-methyl-
 butan-2-ol, 4-phenyl-
2-butanol, 4-phenyl-
2-hydroxy-4-phenyl butane
2-hydroxy-4-phenylbutane
 methyl 2-phenyl ethyl carbinol
 methyl 2-phenylethyl carbinol
alpha-methyl benzene propanol
 methyl phenethyl carbinol
 methyl phenyl ethyl carbinol
 methyl-2-phenylethylcarbinol
a-methylbenzenepropanol
 methylphenethylcarbinol
 phenethyl methyl carbinol
4-phenyl butan-2-ol
 phenyl ethyl methyl carbinol
1-phenyl-3-butanol
4-phenylbutan-2-ol
 phenylethyl methyl carbinol
Synonyms   Articles   Notes   Search   Top
Articles:
PubMed: Online capillary solid-phase microextraction coupled liquid chromatography-mass spectrometry for analysis of chiral secondary alcohol products in yeast catalyzed stereoselective reduction cell culture.
PubMed: Inhibition effects of benzylideneacetone, benzylacetone, and 4-phenyl-2-butanol on the activity of mushroom tyrosinase.
PubMed: Acetophenone reductase with extreme stability against a high concentration of organic compounds or an elevated temperature.
PubMed: Fragrance material review on 2-methyl-4-phenyl-2-butanol.
PubMed: Use of perfluorinated phosphines to provide thermomorphic anticancer complexes for heat-based tumor targeting.
PubMed: A Thermoanaerobacter ethanolicus secondary alcohol dehydrogenase mutant derivative highly active and stereoselective on phenylacetone and benzylacetone.
PubMed: Nonaqueous and halide-free route to crystalline BaTiO3, SrTiO3, and (Ba,Sr)TiO3 nanoparticles via a mechanism involving C-C bond formation.
PubMed: Aminocyclopentadienyl ruthenium complexes as racemization catalysts for dynamic kinetic resolution of secondary alcohols at ambient temperature.
PubMed: Stable isotope characterization of raspberry ketone extracted from Taxus baccata and obtained by oxidation of the accompanying alcohol (Betuligenol).
PubMed: Biotransformation of terodiline I. Identification of metabolites in dog urine by mass spectrometry.
PubMed: The mode of binding of potential transition-state analogs to acetylcholinesterase.
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