diphenyl methane
benzene, (phenylmethyl)-
 
Notes:
None found
  • Augustus Oils
    • Augustus Oils Ltd
      The Premier Supplier
      Augustus Oils Ltd, in harmony with nature - to present it at its best...
      A wealth of experience, expertise and knowledge has allowed Augustus to bridge the gulf in expectation and trust between growers and users of natural ingredients. The Company works in partnership with customers on the one hand, and growers, farmers and distillers on the other. Both users and producers can then focus on exactly what they do best, while skilled Augustus technicians closely monitor and control the delivered product. This ensures users can have the confidence that they will receive the best raw materials suited to their requirements.
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      Diphenyl Methane
       
  • Berjé
    • Berje Inc.
      Where the world comes to its senses
      Where the world comes to its senses - Berjé is a global distributor of Essential Oils and Aromatic Chemicals.
      Berjé is a family-owned business that has been in operation for six decades. The company's origins and strength lie in a profound understanding of the supply and the quality of the diverse raw materials consumed by the flavor and fragrance industries. This base was expanded upon more than two decades ago to include fragrance production. The company's unparalleled raw material expertise is focused on the supply of essential oils and aromatic chemicals. This is supported by our long-standing relationships with a worldwide fabric of producers ensuring the greatest prospects for uninterrupted supply in markets that are often volatile and unpredictable.
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      Diphenyl Methane
       
  • BOC Sciences
    • BOC Sciences
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      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.
      BOC Sciences is a brand of BOCSCI Inc. We leverage our wide spectrum of business in the fields of development, manufacturing, marketing, and distribution to help you make best-informed decisions tailored to your evolving needs for premium chemicals. Our complete suite of CRO services spans the entire molecule development pipeline including contract research for target identification, building blocks, compound synthesis, biochemical and cellular analysis, preclinical animal tests, and clinical studies.
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      Product(s):
      101-81-5 Diphenylmethane
       
  • Lluch Essence
    • Lluch Essence S.L.
      A family company dedicated to sales and distribution
      Flexibility, availability, price and quality.
      Flexibility, availability, price and quality make LLUCH ESSENCE S.L. one of Europe’s references when it comes to essential oils and aroma chemicals, and it is now well known all around the world.
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      DIPHENYL METHANE 98%
       
  • Moellhausen
  • 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):
      04-80700 DIPHENYL METHANE
       
  • SRS Aromatics
    • SRS Aromatics Ltd
      For over 25 years
      Bringing flavour and fragrance into your world.
      As suppliers / distributors of ingredients to the fragrance and flavour industries, our goal is to provide high quality materials at competitive prices with an exceptional level of service. Established in 1984, SRS Aromatics Ltd is an independent family owned business which has become very well-respected within the fragrance and flavour industry as a reliable and trustworthy partner. Over the years this has allowed the company to develop strong relationships with many global manufacturers; several of whom we represent in the UK. A core aim of our business is to work extremely closely with both our suppliers and customers to maximise service levels with minimum disruption to supply.
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  • 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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      W0397 Diphenyl Methane
       
  • 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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      D0896 Diphenylmethane >99.0%(GC)
      SDS
       
  • R C Treatt & Co Ltd
    • R C Treatt and Co Ltd
      Innovative ingredient solutions
      World-leading innovative ingredient solutions provider for the flavour, fragrance and FMCG industries.
      We offer innovative and trend-setting product concepts for our customers, collaborating with them to create true value for their products.
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      Diphenyl Methane
       
Synonyms   Articles   Notes   Search
Fragrance Demo Formulas
CAS Number: 101-81-5Picture of molecule3D/inchi
ECHA EINECS - REACH Pre-Reg: 202-978-6
FDA UNII: K3E387I0BC
Nikkaji Web: J3.597A
Beilstein Number: 1904982
MDL: MFCD00004781
CoE Number: 11847
XlogP3: 4.10 (est)
Molecular Weight: 168.23864000
Formula: C13 H12
BioActivity Summary: listing
NMR Predictor: Predict (works with chrome, Edge or firefox)
EFSA/JECFA Comments: No longer supported by Industry (DG SANCO, 2012).
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 to pale yellow solid (est)
Assay: 95.00 to 100.00 % 
Food Chemicals Codex Listed: No
Melting Point: 25.00 to  27.00 °C. @ 760.00 mm Hg
Boiling Point: 262.00 to  265.00 °C. @ 760.00 mm Hg
Vapor Pressure: 0.016000 mmHg @ 25.00 °C. (est)
Vapor Density: 5.79 ( Air = 1 )
Flash Point: 265.00 °F. TCC ( 129.44 °C. )
logP (o/w): 4.140
Soluble in:
 alcohol
 water, 14.1 mg/L @ 25 °C (exp)
Stability:
 cream
 non-discoloring in most media
 powder
 shampoo
 soap
Synonyms   Articles   Notes   Search   Top
Organoleptic Properties:
 
Odor Type: green
 
Odor Strength: medium ,
recommend smelling in a 10.00 % solution or less
 
Substantivity: 24 hour(s) at 100.00 %
 
 sweet  green  wet  plastic  geranium  
Odor Description:
at 10.00 % in dipropylene glycol. 
sweet green wet plastic geranium
Luebke, William tgsc, (1986)
 
 
Flavor Type: green
 
 green  oily  geranium  spicy  metallic  plastic  privet  pear  
Taste Description:
sweet green oily geranium spicy metallic plastic privet pear
Luebke, William tgsc, (1986)
 
Odor and/or flavor descriptions from others (if found).
 
 
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Cosmetic Information:
CosIng: cosmetic data
Cosmetic Uses: fragrance
solvents
Synonyms   Articles   Notes   Search   Top
Suppliers:
Augustus Oils
Diphenyl Methane
Services
Berjé
Diphenyl Methane
Media
BOC Sciences
For experimental / research use only.
Diphenylmethane
EMD Millipore
For experimental / research use only.
Diphenylmethane
Keva
DIPHENYL METHANE
Odor: Harsh, geranium leaf, orangeblossom
Lluch Essence
DIPHENYL METHANE 98%
Moellhausen
DIPHENYL METHANO
Odor: aromatic oily, slightly floral and spicy on dilution, somewhat rose-like
Flavor: aromatic oily, spicy on dilution
Penta International
DIPHENYL METHANE
R C Treatt & Co Ltd
Diphenyl Methane
Reincke & Fichtner
Diphenylmethane
Santa Cruz Biotechnology
For experimental / research use only.
Diphenylmethane
Sigma-Aldrich: Aldrich
For experimental / research use only.
Diphenylmethane 99%
SRS Aromatics
DIPHENYL METHANE
Synerzine
Diphenyl Methane
TCI AMERICA
For experimental / research use only.
Diphenylmethane >99.0%(GC)
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Safety Information:
Preferred SDS: View
European information :
Most important hazard(s):
Xn - Harmful.
R 22 - Harmful if swallowed.
S 02 - Keep out of the reach of children.
S 20/21 - When using do not eat, drink or smoke.
S 36 - Wear suitable protective clothing.
 
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.
Human Experience:
8 % solution: no irritation or sensitization.
Oral/Parenteral Toxicity:
oral-rat LD50  2250 mg/kg
(Moreno, 1973ai)

oral-rat LD50  2250 mg/kg
Food and Cosmetics Toxicology. Vol. 12, Pg. 705, 1974.

Dermal Toxicity:
skin-rabbit LD50 > 5000 mg/kg
Food and Cosmetics Toxicology. Vol. 12, Pg. 705, 1974.

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 diphenyl methane usage levels up to:
  3.0000 % in the fragrance concentrate.
 
Maximised Survey-derived Daily Intakes (MSDI-EU): 1.20 (μg/capita/day)
Modified Theoretical Added Maximum Daily Intake (mTAMDI): 3900 (μg/person/day)
Threshold of Concern:90 (μg/person/day)
Structure Class: III
 
Food categories according to Commission Regulation EC No. 1565/2000 (EC, 2000) in FGE.06 (EFSA, 2002a). According to the Industry the "normal" use is defined as the average of reported usages and "maximum use" is defined as the 95th percentile of reported usages (EFSA, 2002i).
Note: mg/kg = 0.001/1000 = 0.000001 = 1/1000000 = ppm.
 average usage mg/kgmaximum usage mg/kg
Dairy products, excluding products of category 02.0 (01.0): 7.0000035.00000
Fats and oils, and fat emulsions (type water-in-oil) (02.0): 5.0000025.00000
Edible ices, including sherbet and sorbet (03.0): 10.0000050.00000
Processed fruit (04.1): 7.0000035.00000
Processed vegetables (incl. mushrooms & fungi, roots & tubers, pulses and legumes), and nuts & seeds (04.2): --
Confectionery (05.0): 10.0000050.00000
Chewing gum (05.0): --
Cereals and cereal products, incl. flours & starches from roots & tubers, pulses & legumes, excluding bakery (06.0): 5.0000025.00000
Bakery wares (07.0): 10.0000050.00000
Meat and meat products, including poultry and game (08.0): 2.0000010.00000
Fish and fish products, including molluscs, crustaceans and echinoderms (MCE) (09.0): 2.0000010.00000
Eggs and egg products (10.0): --
Sweeteners, including honey (11.0): --
Salts, spices, soups, sauces, salads, protein products, etc. (12.0): 5.0000025.00000
Foodstuffs intended for particular nutritional uses (13.0): 10.0000050.00000
Non-alcoholic ("soft") beverages, excl. dairy products (14.1): 5.0000025.00000
Alcoholic beverages, incl. alcohol-free and low-alcoholic counterparts (14.2): 10.0000050.00000
Ready-to-eat savouries (15.0): 20.00000100.00000
Composite foods (e.g. casseroles, meat pies, mincemeat) - foods that could not be placed in categories 01.0 - 15.0 (16.0): 5.0000025.00000
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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):
Flavouring Group Evaluation 25, (FGE.25)[1] - Aliphatic and aromatic hydrocarbons from chemical group 31 - Scientific Opinion of the Panel on Food Additives, Flavourings, Processing Aids and Materials in Contact with Food
View page or View pdf
Flavouring Group Evaluation 78 (FGE.78)[1] - Consideration of Aliphatic and alicyclic and aromatic hydrocarbons evaluated by JECFA (63rd meeting) structurally related to aliphatic and aromatic hydrocarbons evaluated by EFSA in FGE.25 - Scientific Opinion of the 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 25Rev1: Aliphatic and aromatic hydrocarbons from chemical group 31
View page or View pdf
Scientific Opinion on Flavouring Group Evaluation 78, Revision 1 (FGE.78Rev1): Consideration of aliphatic and alicyclic and aromatic hydrocarbons evaluated by JECFA (63rd meeting) structurally related to aliphatic and aromatic hydrocarbons evaluated by EFSA in FGE.25Rev2
View page or View pdf
Scientific Opinion on Flavouring Group Evaluation 25, Revision 2 (FGE.25Rev2): Aliphatic and aromatic hydrocarbons from chemical group 31
View page or View pdf
Scientific opinion on Flavouring Group Evaluation 25, Revision 3 (FGE.25Rev3): Aliphatic hydrocarbons from chemical group 31
View page or View pdf
EPI System: View
AIDS Citations: Search
Cancer Citations: Search
Toxicology Citations: Search
EPA Substance Registry Services (TSCA): 101-81-5
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 7580
National Institute of Allergy and Infectious Diseases: Data
WGK Germany: 2
 phenylmethylbenzene
Chemidplus: 0000101815
RTECS: DA4976500 for cas# 101-81-5
Synonyms   Articles   Notes   Search   Top
References:
 phenylmethylbenzene
NIST Chemistry WebBook: Search Inchi
Canada Domestic Sub. List: 101-81-5
Pubchem (cid): 7580
Pubchem (sid): 134971152
Synonyms   Articles   Notes   Search   Top
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: 2902.90.9000
ChemSpider: View
Wikipedia: View
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Potential Blenders and core components note
 
For Odor
aldehydic
 muguet undecadienalFR
balsamic
 benzophenoneFR
 cinnamyl formateFL/FR
citrus
 citral dimethyl acetalFL/FR
(E)-4-decenalFL/FR
 grapefruit pentanolFR
clean
 clean nitrileFR
earthy
1-octen-3-olFL/FR
ethereal
 ethyl formateFL/FR
fatty
2-decenalFL/FR
floral
 amyl benzoateFL/FR
 anisyl propanal / methyl anthranilate schiff's baseFR
alpha-butyl cinnamaldehydeFL/FR
laevo-citronellolFL/FR
 citronellyl acetateFL/FR
 citronellyl propionateFL/FR
(E)-citronellyl tiglateFL/FR
 cumin carbinolFR
 cuminyl acetaldehydeFL/FR
 cyclohexyl ethyl acetateFL/FR
 cyclohexyl ethyl alcoholFL/FR
 cyclohexyl propanolFR
gamma-damasconeFR
 dihydrorose oxideFR
 dimethyl benzyl carbinolFL/FR
 dimethyl benzyl carbinyl butyrateFL/FR
6,8-dimethyl-2-nonanolFR
 ethyl 2-benzyl butyrateFL/FR
 ethyl linaloolFR
 farnesyl acetateFL/FR
 floral butanalFR
 floral pyranFR
 geranium dihydropyranFR
 geranium nitrileFR
 geranium oil africaFL/FR
 geranium oil bourbonFL/FR
 geranium oil egyptFL/FR
 geranium pyranFR
 geranyl acetoneFL/FR
 geranyl formateFL/FR
 geranyl hexanoateFL/FR
 geranyl isobutyrateFL/FR
 geranyl nonanoateCS
 geranyl tiglateFL/FR
(Z)-3-hexen-1-yl salicylateFL/FR
alpha-hexyl cinnamaldehydeFL/FR
 hydroxycitronellalFL/FR
 hydroxycitronellal diethyl acetalFL/FR
 jasmin cyclopentanolFR
 methyl citronellateFL/FR
2-methyl naphthaleneFL/FR
 mimosa absolute franceFL/FR
 muguet carbinolFL/FR
 musk acetateFR
 narcissus acetateFL/FR
 neroli oil bigardeFL/FR
 nerolidolFL/FR
 ocean propanal / methyl anthranilate schiff's baseFR
(Z)-beta-ocimeneFL/FR
 orange leaf absoluteFL/FR
 papaya isobutyrateFL/FR
 peony acetonitrileFR
 phenethyl formateFL/FR
 phenethyl pivalateFL/FR
 phenyl acetaldehyde digeranyl acetalFR
 phenyl acetaldehyde diisobutyl acetalFL/FR
2-phenyl propionaldehyde ethylene glycol acetalFR
 phenyl propyl phenyl acetateFR
 rhodinyl acetateFL/FR
 rhodinyl propionateFL/FR
 rose butanoateFL/FR
(Z)-rose oxideFL/FR
laevo-rose oxideFL/FR
 rose pyranFR
 styralyl formateFL/FR
 terpinyl isobutyrateFL/FR
 verdyl acetateFR
fried
(E,Z)-2,4-decadienal 
fruity
 benzyl methyl etherFL/FR
 citronellyl isobutyrateFL/FR
 dimethyl succinateFL/FR
 ethyl heptanoateFL/FR
 ethyl isovalerateFL/FR
 ethyl methyl-para-tolyl glycidateFL/FR
 octyl formateFL/FR
 peach pivalateFR
green
isoamyl 3-(2-furan) propionateFL/FR
 biphenyl 
isobutyl benzyl carbinolFL/FR
 chrysanthemum oxideFL/FR
 decanal propylene glycol acetalFL/FR
para-dimethyl hydroquinoneFL/FR
 diphenyl oxideFL/FR
 earthy acetalFL/FR
 geranium absoluteFL/FR
 geranium thiazoleFL/FR
1-hepten-3-olFL/FR
(Z)-3-hexen-1-yl butyrateFL/FR
(E)-2-hexen-1-yl butyrateFL/FR
(Z)-3-hexen-1-yl phenyl acetateFL/FR
(E)-2-hexen-1-yl propionateFL/FR
(Z)-3-hexen-1-yl pyruvateFL/FR
 ivy carbaldehyde / methyl anthranilate schiff's baseFR
 ivy dioxolaneFR
 leafy acetalFL/FR
 methyl cyclocitrone (IFF)FR
para-methyl hydratropaldehydeFL/FR
 methyl octine carbonateFL/FR
4-methyl-4-phenyl pentanoneFR
(E,Z)-2,6-nonadienal diethyl acetalFL/FR
 octanal dimethyl acetalFL/FR
 octyl oxyacetaldehydeFR
 olive oil absoluteFL/FR
(Z)-2-penten-1-olFL/FR
 phenethyl isopropyl etherFR
 phenethyl oxyacetaldehydeFR
 phenethyl tiglateFL/FR
 phenyl acetaldehydeFL/FR
herbal
 clary sage absoluteFL/FR
 geranium cyclohexaneFR
3-octyl acetateFL/FR
 sabinene hydrateFL/FR
 theaspiraneFL/FR
leathery
 leather cyclohexanolFR
marine
 marine hexaneFR
spicy
alpha-amyl cinnamyl alcoholFL/FR
terpenic
gamma-terpineneFL/FR
tonka
 coumarinFR
vegetable
1-furfuryl pyrroleFL/FR
waxy
3-decanoneFL/FR
2,4-nonadien-1-olFL/FR
woody
(E)-ethyl geranateFR
 
For Flavor
 
No flavor group found for these
 amyl benzoateFL/FR
(E,Z)-2,4-decadienal 
 decanal propylene glycol acetalFL/FR
3-decanoneFL/FR
 earthy acetalFL/FR
 ethyl 2-benzyl butyrateFL/FR
 styralyl formateFL/FR
 terpinyl isobutyrateFL/FR
isoamyl 3-(2-furan) propionateFL/FR
alpha-butyl cinnamaldehydeFL/FR
amber
isobutyl benzyl carbinolFL/FR
aromatic
 leafy acetalFL/FR
balsamic
 phenethyl pivalateFL/FR
citrus
 citral dimethyl acetalFL/FR
cooling
 sabinene hydrateFL/FR
 theaspiraneFL/FR
cucumber
2-ethyl octine carbonateFL
ethereal
 ethyl formateFL/FR
fatty
2-decenalFL/FR
(E,E)-2,4-heptadienalFL
2,4-nonadien-1-olFL/FR
floral
 biphenyl 
laevo-citronellolFL/FR
 citronellyl acetateFL/FR
 citronellyl propionateFL/FR
 dimethyl benzyl carbinyl butyrateFL/FR
 farnesyl acetateFL/FR
 geranium oil africaFL/FR
 geranium oil bourbonFL/FR
 geranium oil egyptFL/FR
 geranyl acetoneFL/FR
 geranyl isobutyrateFL/FR
 geranyl tiglateFL/FR
 methyl citronellateFL/FR
 muguet carbinolFL/FR
 neroli oil bigardeFL/FR
 orange leaf absoluteFL/FR
 rhodinyl acetateFL/FR
laevo-rose oxideFL/FR
fruity
 benzyl methyl etherFL/FR
 citronellyl isobutyrateFL/FR
 dimethyl succinateFL/FR
 ethyl heptanoateFL/FR
 ethyl isovalerateFL/FR
 ethyl methyl-para-tolyl glycidateFL/FR
 geranyl hexanoateFL/FR
 rhodinyl propionateFL/FR
 rose butanoateFL/FR
green
 chrysanthemum oxideFL/FR
(E)-citronellyl tiglateFL/FR
 cuminyl acetaldehydeFL/FR
 cyclohexyl ethyl acetateFL/FR
 cyclohexyl ethyl alcoholFL/FR
(E)-4-decenalFL/FR
para-dimethyl hydroquinoneFL/FR
 diphenyl oxideFL/FR
2-ethyl-5-methyl thiopheneFL
 geranium absoluteFL/FR
 geranium thiazoleFL/FR
 geranyl formateFL/FR
1-hepten-3-olFL/FR
(Z)-3-hexen-1-yl butyrateFL/FR
(E)-2-hexen-1-yl butyrateFL/FR
(Z)-3-hexen-1-yl phenyl acetateFL/FR
(E)-2-hexen-1-yl propionateFL/FR
(Z)-3-hexen-1-yl pyruvateFL/FR
(Z)-3-hexen-1-yl salicylateFL/FR
 methyl 2-undecynoateFL
para-methyl hydratropaldehydeFL/FR
 methyl octine carbonateFL/FR
 narcissus acetateFL/FR
 nerolidolFL/FR
(E,Z)-2,6-nonadienal diethyl acetalFL/FR
(Z)-beta-ocimeneFL/FR
 octanal dimethyl acetalFL/FR
3-octyl acetateFL/FR
 octyl formateFL/FR
 papaya isobutyrateFL/FR
(Z)-2-penten-1-olFL/FR
4-penten-1-yl acetateFL
 phenethyl formateFL/FR
 phenethyl tiglateFL/FR
 phenyl acetaldehyde diisobutyl acetalFL/FR
(Z)-rose oxideFL/FR
herbal
 clary sage absoluteFL/FR
honey
 phenyl acetaldehydeFL/FR
medicinal
 dimethyl benzyl carbinolFL/FR
melon
 hydroxycitronellal diethyl acetalFL/FR
mushroom
1-octen-3-olFL/FR
oily
2-methyl naphthaleneFL/FR
 olive oil absoluteFL/FR
spicy
alpha-amyl cinnamyl alcoholFL/FR
 cinnamyl formateFL/FR
terpenic
gamma-terpineneFL/FR
vegetable
1-furfuryl pyrroleFL/FR
waxy
alpha-hexyl cinnamaldehydeFL/FR
 hydroxycitronellalFL/FR
 mimosa absolute franceFL/FR
 
Synonyms   Articles   Notes   Search   Top
Potential Uses:
 appleFR
 bananaFR
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Occurrence (nature, food, other): note
 not found in nature
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Synonyms:
 benzene, (phenylmethyl)-
 benzyl benzene
 benzylbenzene
 diphenyl methano
 diphenylmethane
 methane, diphenyl-
1,1'-methanediyldibenzene
1,1'-methylene bisbenzene
1,1'-methylenebis[benzene]
1,1'-methylenebisbenzene
1,1'-methylenedibenzene
alpha-phenyl toluene
(phenylmethyl)benzene
 phenylmethylbenzene
a-phenyltoluene
alpha-phenyltoluene
 toluene, a-phenyl-
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