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General Material Information

Preferred name raspberry ketone
Trivial Name 4-(4′-Hydroxyphenyl)-2-butanone
Short Description 4-(p-hydroxyphenyl)-2-butanone
Formula C10 H12 O2
CAS Number 5471-51-2
Deleted CAS Number 1039415-63-8
FEMA Number 2588
Flavis Number 7.055
ECHA Number 226-806-4
FDA UNII 7QY1MH15BG
Nikkaji Number J31.103K
Beilstein Number 0776080
MDL MFCD00002394
COE Number 755
xLogP3-AA 1.50 (est)
Bio Activity Summary External link
NMR Predictor External link
JECFA Food Flavoring 728 4-(p-hydroxyphenyl)-2-butanone
FDA Patent No longer provide for the use of these seven synthetic flavoring substances
FDA Mainterm 5471-51-2 ; 4-(P-HYDROXYPHENYL)-2-BUTANONE
Synonyms
  • butan-2-one, 4-(4-hydroxyphenyl)-
  • 2-butanone, 4-(4-hydroxyphenyl)-
  • 2-butanone, 4-(p-hydroxyphenyl)-
  • 4-(3-oxo butyl) phenol
  • 4-(3-oxo butyl)phenol
  • frambinone
  • p- hydrobenzyl acetone
  • para- hydrobenzyl acetone
  • 4 hydroxy phenyl-2-butanone
  • 4-hydroxy-4-phenylbutan-2-one
  • 4-(4-hydroxy-phenyl)-butan-2-one
  • p- hydroxybenzyl acetone
  • para- hydroxybenzyl acetone
  • (p- hydroxybenzyl)acetone
  • 4-hydroxybenzylacetone
  • p- hydroxybenzylacetone
  • 1-p- hydroxyphenyl-3-butanone
  • 1-para- hydroxyphenyl-3-butanone
  • 4-(4-hydroxyphenyl) butan-2-one
  • 4-(4-hydroxyphenyl)-2-butanone
  • 4-(p- hydroxyphenyl)-2-butanone
  • 4-(para- hydroxyphenyl)-2-butanone
  • 4-(4-hydroxyphenyl)-2-butanone natural
  • 1-(4-hydroxyphenyl)-3-butanone
  • 1-(p- hydroxyphenyl)-3-butanone
  • 1-(para- hydroxyphenyl)-3-butanone
  • 4-(para- hydroxyphenyl)2-butanone
  • 4-(4-hydroxyphenyl)butan-2-one
  • 4-(p- hydroxyphenyl)butan-2-one
  • 2-(4-hydroxyphenyl)ethyl methyl ketone
  • hydroxyphenylbutanone, p-
  • N 112
  • N112
  • oxanone
  • oxy phenylon
  • rasketone
  • nat. raspberry ketone
  • raspberry ketone (natural)
  • raspberry ketone FCC
  • raspberry ketone natural
  • raspberry ketone recrystallized
  • raspberry ketone synthetic
  • raspberry keytone
  • rastone
  • rheosmin
  • 4-(4-hydroxyphenyl)butan-2-one
  • 2-Butanone, 4-(4-hydroxyphenyl)-
  • 2-Butanone, 4-(p-hydroxyphenyl)-
  • 4-(4-Hydroxyphenyl)-2-butanone
  • (p-Hydroxybenzyl)acetone
  • 4-(p-Hydroxyphenyl)-2-butanone
  • 1-(p-Hydroxyphenyl)-3-butanone
  • 1-(4-Hydroxyphenyl)-3-butanone
  • 4-(4′-Hydroxyphenyl)-2-butanone
  • 4-(3-Oxobutyl)phenol
  • Oxyphenylon
  • (4-Hydroxybenzyl)acetone
  • NSC 26515
  • 4-(4-Hydroxy-1-phenyl)-2-butanone

US / EU / FDA / JECFA / FEMA / Scholar / Patents

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Literature & References

4-(4-hydroxyphenyl)butan-2-one
NIST Chemistry WebBook:Search Inchi
Canada Domestic Sub. List:5471-51-2
Pubchem (cid):21648
Pubchem (sid):134986252
Flavornet:5471-51-2
Pherobase:View
Publications by Info
Raspberry Ketone
Publications by PubMed
Raspberry ketone promotes the differentiation of C3H10T1/2 stem cells into osteoblasts.
Raspberry ketone protects rats fed high-fat diets against nonalcoholic steatohepatitis.
Characterization of raspberry ketone/zingerone synthase, catalyzing the alpha, beta-hydrogenation of phenylbutenones in raspberry fruits.
Field trials of solid triple lure (trimedlure, methyl eugenol, raspberry ketone, and DDVP) dispensers for detection and male annihilation of Ceratitis capitata, Bactrocera dorsalis, and Bactrocera cucurbitae (Diptera: Tephritidae) in Hawaii.
The metabolism of 4-(4-hydroxyphenyl)butan-2-one (raspberry ketone) in rats, guinea-pigs and rabbits.
A labeling study to elucidate the biosynthesis of 4-(4-hydroxyphenyl)-butan-2-one (raspberry ketone) by Nidula niveo-tomentosa.
Evaluation of in Vitro and in Vivo Depigmenting Activity of Raspberry Ketone from Rheum officinale.
Effect of essential oils, such as raspberry ketone and its derivatives, on antiandrogenic activity based on in vitro reporter gene assay.
Raspberry ketone increases both lipolysis and fatty acid oxidation in 3T3-L1 adipocytes.
Microbial production of 4-hydroxybenzylidene acetone, the direct precursor of raspberry ketone.
Raspberry ketone from submerged cultured cells of the basidiomycete Nidula niveo-tomentosa.
Microbial production of natural raspberry ketone.
Effect of topical application of raspberry ketone on dermal production of insulin-like growth factor-I in mice and on hair growth and skin elasticity in humans.
Anti-obese action of raspberry ketone.
Field captures of wild melon fly (Diptera: Tephritidae) with an improved male attractant, raspberry ketone formate.
Recent advances in methyl eugenol and cue-lure technologies for fruit fly detection, monitoring, and control in Hawaii.
Production and elicitation of benzalacetone and the raspberry ketone in cell suspension cultures of Rubus idaeus.
Biotransformation of raspberry ketone and zingerone by cultured cells of Phytolacca americana.
Synomone or kairomone?--Bulbophyllum apertum flower releases raspberry ketone to attract Bactrocera fruit flies.
Stable isotope characterization of raspberry ketone extracted from Taxus baccata and obtained by oxidation of the accompanying alcohol (Betuligenol).
Natural Abundance (2)H Nuclear Magnetic Resonance Study of the Origin of Raspberry Ketone.
Characterization of headspace aroma compounds of freshly brewed arabica coffees and studies on a characteristic aroma compound of Ethiopian coffee.
[Determination of four n-butyrophenone compounds contained in rhubarb using RP-HPLC].
Dietary exposure to flavouring substances: from screening methods to detailed assessments using food consumption data collected with EPIC-Soft software.
[Non-taxoid chemical constituents from needles of Taxus cuspidata].
Frequently asked questions of the Academy's knowledge center.
Eight weeks of supplementation with a multi-ingredient weight loss product enhances body composition, reduces hip and waist girth, and increases energy levels in overweight men and women.
Environmental and seasonal influences on red raspberry flavour volatiles and identification of quantitative trait loci (QTL) and candidate genes.
Trap capture of three economically important fruit fly species (Diptera: Tephritidae): evaluation of a solid formulation containing multiple male lures in a Hawaiian coffee field.
Ultra-performance LC-photodiode array-eλ-ESI-MS/MS screening method for the detection of radical-scavenging natural antioxidants from radix et rhizoma Rhei.
Characterization of the bound volatile extract from baby kiwi (Actinidia arguta).
Analysis of the headspace volatiles of freshly brewed arabica coffee using solid-phase microextraction.
Response of melon fly (Diptera: Tephritidae) to weathered SPLAT-Spinosad-Cue-Lure.
Rheosmin, a naturally occurring phenolic compound inhibits LPS-induced iNOS and COX-2 expression in RAW264.7 cells by blocking NF-kappaB activation pathway.
Purification and biological evaluation of the metabolites produced by Streptomyces sp. TK-VL_333.
Prolyl endopeptidase inhibitory activity of fourteen Kampo formulas and inhibitory constituents of Tokaku-joki-to.
Evaluation of methyl eugenol and cue-lure traps with solid lure and insecticide dispensers for fruit fly monitoring and male annihilation in the Hawaii Areawide Pest Management Program.
Stress response of Nidula niveo-tomentosa to UV-A light.
Phenols from the roots of Rheum palmatum attenuate chemotaxis in rat hepatic stellate cells.
Dual-enzyme cascade--an amplified method for the detection of alkaline phosphatase.
Volatile composition in raspberry cultivars grown in the Pacific Northwest determined by stir bar sorptive extraction-gas chromatography-mass spectrometry.
Effect of high hydrostatic pressure on the barrier properties of polyamide-6 films.
Lipolytic effects of citrus peel oils and their components.
Aroma extract dilution analysis of cv. Meeker (Rubus idaeus L.) red raspberries from Oregon and Washington.
Cytotoxic and DNA damage-inducing activities of low molecular weight phenols from rhubarb.
Accumulation ofDendrobium superbum (orchidaceae) fragrance in the rectal glands by males of the melon fly,Dacus cucurbitae.
Betuligenol derivative with growth inhibition and antifeedant activity.
Progress in synthesis of sensory important trace components of essential oils and natural flavours.
Aroma production by tissue cultures.
Olfactory receptors in the melon fly Dacus cucurbitae and the oriental fruit fly Dacus dorsalis.

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
CHEBI:View
CHEMBL:View
HMDB (The Human Metabolome Database):HMDB33723
FooDB:FDB011843
Export Tariff Code:2914.50.3000
VCF-Online:VCF Volatile Compounds in Food
ChemSpider:View
Wikipedia:View

Suppliers

ACS International Advanced Biotech
Alfa Biotechnology Alfrebro
Ambles Nature et Chimie Anhui Haibei
Aromiens International Artiste
Astral Extracts Augustus Oils
Aurochemicals Axxence Aromatic
Beijing Lys Chemicals Bell Flavors & Fragrances
Berjé BOC Sciences
Citrus and Allied Essences CJ Latta & Associates
Creatingperfume.com De Monchy Aromatics
ECSA Chemicals Elan Inc.
Ernesto Ventós Excellentia International
ExtraSynthese Fleurchem
Foreverest Resources Frey + Lau
Fuzhou Farwell Global Essence
H. Interdonati, Inc. Indenta Group
Indukern F&F Jiangyin Healthway
John Kellys (London) K.L. Koh Enterprise
Kingchem Laboratories Kun Shan P&A
Lluch Essence M&U International
Moellhausen O'Laughlin Industries
Oamic Ingredients Omega Ingredients
OQEMA PCW France
Pearlchem Corporation Pell Wall Perfumes
Penta International PerfumersWorld
Perfumery Laboratory Phoenix Aromas & Essential Oils
Prasad Organics Primechem
Prinova Prodasynth
Quimdis R C Treatt & Co Ltd
Reincke & Fichtner Sigma-Aldrich
SRS Aromatics Sunaux International
Synerzine TCI AMERICA
Tengzhou Xiang Yuan Aroma Chemicals The John D. Walsh Company
The Lermond Company The Perfumers Apprentice
Tianjin Danjun International United International
Vigon International WEN International
WholeChem Zanos
ACS International GmbH Advanced Biotech. Inc.
Alfrebro LLC/ Archer Daniels Midland Company Augustus Oils Ltd
Axxence Aromatic GmbH Beijing Lys Chemicals Co, LTD.
Berje Inc. CJ Latta & Associates, LLC
Fleurchem, Inc. Foreverest Resources Ltd.
Global Essence Inc. Indukern, S.A. F&F Ingredients Division
Jiangyin Healthway International Trade Co., Ltd Lluch Essence S.L.
M&U International LLC Moellhausen S.P.A.
O'Laughlin Industries Inc. Penta International Corporation
PerfumersWorld Ltd. Anhui Primechem Co., Ltd.
SRS Aromatics Ltd Synerzine, Inc.
The John D. Walsh Company, Inc Tianjin Danjun International Trade Co., LTD.
R C Treatt and Co Ltd Qingdao Free Trade Zone United International Co Ltd
Ernesto Ventós S.A. WholeChem, LLC
Zanos Ltd.

PhysChem Properties

Material listed in food chemical codex Yes
Molecular weight 164.20404052734
Melting Point 82 to 84°C @ 760 mm Hg
Vapor Pressure 0.001 mmHg @ 25 °C
Flash Point TCC Value 93.33 °C TCC
logP (o/w) 1.309 est
Shelf life 24 months (or longer if stored properly.)
Storage notes Store in cool, dry place in tightly sealed containers, protected from heat and light.
Solubility
alcohol Yes
dipropylene glycol Yes
propylene glycol Yes
water, very slightly Yes
water, 1.346e+004 mg/L @ 25 °C (est) Yes
paraffin oil No
isopropyl myristate No

Organoleptic Properties

Odor Type: Berry
sweet, berry, jammy, raspberry, ripe, floral, woody, seedy
Odor strength medium , recommend smelling in a 10.00 % solution or less
Substantivity 400 hour(s) at 20.00 % in dipropylene glycol
Luebke, William tgsc, (1992) At 10.00 % in dipropylene glycol. sweet berry jam raspberry ripe floral
Mosciano, Gerard P&F 22, No. 1, 57, (1997) Berry, sweet, woody and raspberry with a ripe, jammy, seedy character
Flavor Type: Berry
fruity, jammy, berry, raspberry, blueberry, seedy, cotton candy
Mosciano, Gerard P&F 22, No. 1, 57, (1997) At 40.00 ppm. Fruity, jammy, berry, raspberry and blueberry with seedy, cotton candy nuances
General comment Strong, fruity, raspberry in dilution

Occurrences

Safety Information

Safety information

Preferred SDS: View
European information :
Most important hazard(s):
Xn - Harmful.
R 22 - Harmful if swallowed.
R 36/38 - Irritating to skin and eyes.
S 02 - Keep out of the reach of children.
S 24/25 - Avoid contact with skin and eyes.
S 36 - Wear suitable protective clothing.
Hazards identification
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
Acute toxicity, Oral (Category 4), H302
GHS Label elements, including precautionary statements
Pictogramexclamation-mark.jpg
Signal word Warning
Hazard statement(s)
H302 - Harmful if swallowed
Precautionary statement(s)
P264 - Wash skin thouroughly after handling.
P270 - Do not eat, drink or smoke when using this product.
P301 + P312 - IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.
P330 - Rinse mouth.
P501 - Dispose of contents/ container to an approved waste disposal plant.
Human Experience:
12 % solution: no irritation or sensitization.
Oral/Parenteral Toxicity:
gavage-rat LD50 [sex: M,F] M: 1320 mg/kg
(Gaunt et al., 1970)

intraperitoneal-rat LD50 350 mg/kg
Food and Cosmetics Toxicology. Vol. 8, Pg. 349, 1970.

oral-rat LD50 > 5000 mg/kg
(Mc Gee Laboratories, Inc., 1974)

gavage-rat LD50 [sex: M,F] F: 1400 mg/kg
(Gaunt et al., 1970)

oral-rat LD50 1320 mg/kg
BEHAVIORAL: ALTERED SLEEP TIME (INCLUDING CHANGE IN RIGHTING REFLEX) BEHAVIORAL: ANALGESIA
Food and Cosmetics Toxicology. Vol. 8, Pg. 349, 1970.

intraperitoneal-rat LD50 350 mg/kg
BEHAVIORAL: ALTERED SLEEP TIME (INCLUDING CHANGE IN RIGHTING REFLEX) BEHAVIORAL: ANALGESIA
Food and Cosmetics Toxicology. Vol. 8, Pg. 349, 1970.

Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined

Safety in use information

Category:
cosmetic, 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
IFRA Critical Effect:
Depigmentation
View the IFRA Standard
View IFRA Standards Library for complete information.
Please review Amendment 49 IFRA documentation for complete information.
IFRA RESTRICTION LIMITS IN THE FINISHED PRODUCT (%):
Category 1: Products applied to the lips
0.68 %
Category 2: Products applied to the axillae
1.00 %
Category 3: Products applied to the face/body using fingertips
0.27 %
Category 4: Products related to fine fragrance
1.00 %
Category 5: Products applied to the face and body using the hands (palms), primarily leave-on
Category 5A: Body lotion products applied to the body using the hands (palms), primarily leave-on
1.00 %
Category 5B: Face moisturizer products applied to the face using the hands (palms), primarily leave-on
0.14 %
Category 5C: Hand cream products applied to the hands using the hands (palms), primarily leave-on
0.27 %
Category 5D: Baby Creams, baby Oils and baby talc
0.045 %
Category 6: Products with oral and lip exposure
0.82 %
Category 7: Products applied to the hair with some hand contact
Category 7A: Rinse-off products applied to the hair with some hand contact
0.41 %
Category 7B: Leave-on products applied to the hair with some hand contact
0.41 %
Category 8: Products with significant anogenital exposure
0.045 %
Category 9: Products with body and hand exposure, primarily rinse off
1.00 %
Category 10: Household care products with mostly hand contact
Category 10A: Household care excluding aerosol products (excluding aerosol/spray products)
1.00 %
Category 10B: Household aerosol/spray products
1.00 %
Category 11: Products with intended skin contact but minimal transfer of fragrance to skin from inert substrate
Category 11A: Products with intended skin contact but minimal transfer of fragrance to skin from inert substrate without UV exposure
0.045 %
Category 11B: Products with intended skin contact but minimal transfer of fragrance to skin from inert substrate with potential UV exposure
0.045 %
Category 12: Products not intended for direct skin contact, minimal or insignificant transfer to skin
78.00 %
Notes:
IFRA FLAVOR REQUIREMENTS:

Due to the possible ingestion of small amounts of fragrance ingredients from their use in products in Categories 1 and 6, materials must not only comply with IFRA Standards but must also be recognized as safe as a flavoring ingredient as defined by the IOFI Code of Practice (www.iofi.org). For more details see chapter 1 of the Guidance for the use of IFRA Standards.

Maximised Survey-derived Daily Intakes (MSDI-EU): 2400.00 (μg/capita/day)
Maximised Survey-derived Daily Intakes (MSDI-USA): 3800.00 (μg/capita/day)
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. Update in publication number(s): 29
Click here to view publication 3
average usual ppmaverage maximum ppm
baked goods: 13.0000054.00000
beverages(nonalcoholic): 3.0000016.00000
beverages(alcoholic): 250.00000300.00000
breakfast cereal: --
cheese: --
chewing gum: 71.00000320.00000
condiments / relishes: --
confectionery froastings: --
egg products: --
fats / oils: --
fish products: --
frozen dairy: 9.0000034.00000
fruit ices: --
gelatins / puddings: 14.0000050.00000
granulated sugar: --
gravies: --
hard candy: 17.0000044.00000
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: 13.0000036.00000
soups: --
sugar substitutes: --
sweet sauces: 0.900001.00000

Safety references

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 22 (FGE.22): Ring-substituted phenolic substances from chemical groups 21 and 25 (Commission Regulation (EC) No 1565/2000 of 18 July 2000)
View page or View pdf

Flavouring Group Evaluation 58 (FGE.58) Consideration of phenol derivatives evaluated by JECFA (55th meeting) structurally related to ring substituted phenolic substances evaluated by EFSA in FGE.22 (2006) (Commission Regulation (EC) No 1565/2000 of 18 July 2000) - Opinion of the Scientific Panel on Food Additives, Flavourings, Processing Aids and Materials in contact with Food (AFC)
View page or View pdf

Scientific Opinion on Flavouring Group Evaluation 22, Revision 1 (FGE.22Rev1): Ring-substituted phenolic substances from chemical groups 21 and 25
View page or View pdf

Safety and efficacy of aromatic ketones, secondary alcohols and related esters belonging to chemical group 21 when used as flavourings for all animal species
View page or View pdf

Safety of 31 flavouring compounds belonging to different chemical groups when used as feed additives for all animal species
View page or View pdf

EPI System: View
AIDS Citations:Search
Cancer Citations:Search
Toxicology Citations:Search
EPA Substance Registry Services (TSCA):5471-51-2
EPA ACToR:Toxicology Data
EPA Substance Registry Services (SRS):Registry
Laboratory Chemical Safety Summary :21648
National Institute of Allergy and Infectious Diseases:Data
WGK Germany:2
4-(4-hydroxyphenyl)butan-2-one
Chemidplus:0005471512
RTECS:EL8925000 for cas# 5471-51-2