lilyall
lilial
 
Notes:
fresh accord - lilyall and benzyl isoeugenol. autumn leaves accord - phenethyl phenyl acetate and lilyall and raspberry ketone. clean fresh accord - aldehyde C-12 10% and lilyall. cloth accord - musk gx, alcohol C-12, lilyall and santall.
  • 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.
      Email: Enquiries
      Email: Sales
      Email: web site enquiries
      Voice: +44 (0)1420 590555
      Fax: +44 (0)1420 592420
      Services
      Product(s):
      Lilial
       
  • 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.
      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.
      Email: Marketing
      US Email: Marketing
      Email: Sales
      US Email: Sales
      Voice: 1-631-504-6093
      Fax: 1-631-614-7828
      US Voice: 1-631-504-6093
      US Fax: 1-631-614-7828
      Europe44-203-286-1088
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      Product(s):
      80-54-6 3-(4-tert-Butylphenyl)-2-methylpropionaldehyde
       
  • ECSA Chemicals
    • ECSA Chemicals
      International trading and distribution
      ECSA Group offers its customers in these business segments a complete 'one-stop shopping' solution.
      A hundred years on from its establishment, the Emanuele Centonze Holding SA has developed a solid presence in Switzerland and in Europe. The Group currently includes: ECSA Chemicals AG/ECSA Italia SRL SocietÓ con Unico Socio – ECSA Maintenance AG – ECSA Energy SA – Porta Ticino Easy Stop SA.
      Email: Info
      Email: Sales
      Email: Trading
      Email: Maintenance
      Email: Energy
      Voice: +41 91 695 88 00
      Fax: +41 91 695 88 01
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      Company Profile
      Products List: View
      Product(s):
      Lilial
       
  • Global Essence
    • Global Essence Inc.
      Preferred Partner
      Accommodate each customers unique needs.
      Global Essence was founded in 1993 as a two person operation servicing regional customers in the New York/ New Jersey area. In the twenty years since, it has grown into a multinational operation with offices in the US, UK, and Singapore. These offices allow Global to provide regional support to its customers worldwide. As the world continues become more connected, this approach positions Global to continue to offer the highest quality products and experience to all of its customers.
      Email: Info
      US Email: Info
      Voice: +44 (0) 1279 876666
      Fax: +44 (0)1279 876646
      US Voice: 001 732 677 1100
      US Fax: 001 732 677 1107
      Blog
      Press Release
      News
      Product(s):
      Lilial
       
  • Indukern F&F
  • 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.
      Email: Info
      Voice: 34 93 379 38 49
      Fax: 34 93 370 65 04
      Linkedin
      Product(s):
      LILIAL
       
  • Moellhausen
  • Pell Wall Perfumes
    • Pell Wall Perfumes
      Hand-made fragrances
      Pell Wall maintains a broad palette of ingredients & in order to keep stocks fresh & the options wide we also sell from our own stock.
      Pell Wall was founded by perfumer Chris Bartlett to provide exclusive hand-made fragrances to a select few people who love them. All our products are created using fine quality ingredients, many of which we also offer for sale to other perfumers and enthusiasts. Pell Wall make fragrances for men, for women and for the home.
      Email: Info
      Email: Sales
      Voice: +44 1630 652546
      Mobile+44 7792 580511
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      Product(s):
      Lilial
       
  • 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.
      US Email: Technical Services
      US Email: Sales
      US Voice: (973) 740-2300
      US Fax: (973) 740-1839
      Product(s):
      12-39500 LILIAL
      12-39501 LILIAL REGULAR
       
  • PerfumersWorld
    • PerfumersWorld Ltd.
      feeeel... the smell!
      The one-stop resource for the creative perfumer.
      No minimum orders. Aroma chemicals, essential oils, isolates, pheremones, absolutes, resinoids, FleuressenceTM key bases, PWx FactorTM, solubilizers, kits, creation systems, workshops, training, distance learning, The PerfumersWorld Perfumer's Studio, The Perfumer’s Formulation Bulletin, perfumery software, bespoke creation, analysis, consultancy, project counselling, trouble-shooting, unperfumed product bases, bottles, smelling strips, scales, distillation, equipment and inspiration!
      Email: Enquiries
      Email: Sales
      Voice: +66(0)2-99-800-80
      Fax: +66(0)2-99-800-80
      PerfumersWorld Skype Skype
      Facebook
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      Resources
      Software: Perfumer's Workbook
      Product(s):
      3MA00273 Lilial
       
  • Phoenix Aromas & Essential Oils
    • Phoenix Aromas & Essential Oils, Inc.
      EXCEPTIONAL Flavor and Fragrance Ingredients.
      Phoenix sources the finest flavor and fragrance ingredients for its customers.
      Phoenix Aromas & Essential Oils LLC was founded in 1994, grounded in a simple set of core values: provide top-quality products, cost-effective pricing and personalized attention to all our customers.
      Email: EU Info
      US Email: Info
      US Email: Sales
      Voice: +44(0) 208 532 1022
      Fax: +44(0) 208 532 1023
      US Voice: 201-784-6100
      US Fax: 201-784-8566
      Global Reach
      Product(s):
      Lilial
       
  • Prodasynth
    • Prodasynth
      PRODUCTEUR PAR ESSENCE
      Chemical specialist in manufacturing, distributing and sourcing of tailor-made ingredients for the Flavour & Fragrance industry.
      Today we are also proud to say, we have created an important range of Natural Molecules which can be found in our Raw Material Compendium. The versatility of our small but efficient structure is one of our main strengths when trying to fulfill our clients' requirements.
      Email: Info:
      Email: Karine Cohen
      Voice: (33) 4 93 09 00 11
      Fax: (33) 4 22 13 07 38
      New Catalog
      Products List: View
      Product(s):
      LILIAL (> 99%
       
  • 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.
      Email: Info
      Email: Sales
      Voice: +44 (0) 1284 704076
      Fax: +44 (0) 1284 760819
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      Product(s):
      LILIALDEHYDE
       
  • Taytonn
    • TAYTONN PTE LTD
      Supplying Asia Pacific
      We fully understand the demands of the F&F industry and we endeavour to supply quality products, with ready availability and a personalised service.
      Since 2001 TAYTONN has been distributing key ingredients to the Fragrance and Flavor industry in Asia. We work closely with customers, principals and vendors. Together we forecast demand and match it with supply of aroma chemicals, essential oils and natural isolates & extracts. Sourced from around the world, our F&F ingredient inventory in Singapore is ready to ship to any location in Asia and beyond. Time and again, we help our principals introduce new discoveries to the F&F market - stimulating creativity and bringing value added proposition to our customers.
      Email: Info
      Email: Sales
      Voice: + 65 - 6861 8113
      Fax: + 65 - 6861 8115
      Product(s):
      Lilestralis®
       
  • 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 28,000 Reagents available today in benchtop to bulk quantities. 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 60 years of synthesis experience and multi-purpose plants enable TCI to offer more than 28,000 products as well as custom synthesis. TCI has established overseas facilities in North America, Europe, China and India to serve customers worldwide.
      US Email: Sales
      Email: Technical Support
      Voice: 1-800-423-8616
      Fax: 1- 888-520-1075
      Facebook
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      RSS
      Product(s):
      B1145 3-(4-tert-Butylphenyl)isobutyraldehyde >96.0%(GC)
       
  • The Good Scents Company
  • The John D. Walsh Company
    • The John D. Walsh Company, Inc
      Suppliers Since 1942
      Supplying the fragrance and flavor industry with high quality products.
      The John D. Walsh Company, Inc. has evolved from its beginnings as an agent/broker into a distributor of essential oils, aroma chemicals, concretes and absolutes. We currently represent the following companies, as their North American distributor: Destilerias Munoz Galvez, S.A. International Flavors & Fragrances PFW Aroma Chemicals B.V. Innospec Widnes Limited Hydrodiffusion de Guatemala, S. A. DSM Nutritional Products The John D. Walsh Company, Inc. is proud to be a founding member of IFEAT, an active member of IFRA, North America, and a corporate sponsor of the WFFC.
      Email: Information
      Email: Sales
      Email: Firmenich Flavor inquiries
      Voice: 973-962-1400
      Fax: 973-962-1557
      Firmenich Flavor Phone:973-962-1888
      Firmenich Flavor Fax:973-962-1898
      History
      Product(s):
      Mefloral
      Lilestralis
      SDS
       
  • The Lermond Company
    • The Lermond Company
      Your Sourcing Resource
      The Lermond family has been sourcing raw materials for the flavor and fragrance industry for nearly 7 decades.
      The Lermond Company is a women-owned distributor of raw materials primarily servicing the flavor and fragrance industry. For three generations, members of the Lermond family have been integral sourcing partners for the North American flavor and fragrance industry. We supply high quality essential oils, aroma chemicals, absolutes, concretes, resinoids and floral waters from around the world to the global industry.
      Email: Info
      Email: Tara
      Email: Erica
      Voice: 201-896-3300
      Fax: 201-623-2910
      Facebook
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      Product(s):
      38749 LILIAL
       
  • Ernesto Ventós
  • Vigon International
    • Vigon International, Inc.
      Passion for Simplicity
      Manufacturer and supplier of high quality flavor and fragrance ingredients.
      The growth and success of Vigon is due in large part to a unique corporate concept that Vigon has developed and established within the industry: Creative Partnerships. This partnership concept has been and continues to be the foundation and guiding principle for all of Vigon's activities.
      US Email: Sales
      US Voice: 570-476-6300
      US Fax: 570-476-1110
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      Products List: View
      Product(s):
      503750 Lysmeral Extra (Lilial)
       
Synonyms   Articles   Notes   Search
Fragrance Demo Formulas
CAS Number: 80-54-6Picture of molecule3D/inchi
Other: 39390-70-0
ECHA EINECS - REACH Pre-Reg: 201-289-8
FDA UNII: T7540GJV69
Nikkaji Web: J560.043J
Beilstein Number: 0880140
MDL: MFCD00047655
XlogP3-AA: 3.60 (est)
Molecular Weight: 204.31260000
Formula: C14 H20 O
BioActivity Summary: listing
NMR Predictor: Predict (works with chrome or firefox)
Category: 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
Synonyms   Articles   Notes   Search   Top
Physical Properties:
Appearance: colorless to pale yellow clear oily liquid (est)
Assay: 93.00 to 100.00 % 
Food Chemicals Codex Listed: No
Specific Gravity: 0.94200 to 0.94700 @  25.00 °C.
Pounds per Gallon - (est).: 7.838 to  7.880
Refractive Index: 1.50300 to 1.50600 @  20.00 °C.
Boiling Point: 250.00 to  251.00 °C. @ 750.00 mm Hg
Boiling Point: 126.00 to  127.00 °C. @ 6.00 mm Hg
Acid Value: 2.00 max. KOH/g
Vapor Pressure: 0.005000 mmHg @ 25.00 °C. (est)
Flash Point: 210.00 °F. TCC ( 98.89 °C. )
logP (o/w): 4.216 (est)
Shelf Life: 24.00 month(s) or longer if stored properly.
Storage: store in cool, dry place in tightly sealed containers, protected from heat and light. store under nitrogen.
Storage: store under nitrogen.
Soluble in:
 alcohol
 paraffin oil
 water, 38 mg/L @ 20 °C (exp)
Insoluble in:
 water
Stability:
 detergent
 soap
Synonyms   Articles   Notes   Search   Top
Organoleptic Properties:
 
Odor Type: floral
 
Odor Strength: medium
 
Substantivity: 236 hour(s) at 100.00 %
 
 floral  muguet  watery  green  powdery  cumin  
Odor Description:
at 100.00 %. 
floral muguet watery green powdery cumin
Luebke, William tgsc, (1986)
 
Odor and/or flavor descriptions from others (if found).
 
Indukern F&F
LILESTRALIS PURE
Odor Description: FRESH, GREEN, FLORAL, LILAC
 
Prodasynth
LILIAL (> 99%
Odor Description: FRESH, LIGHT, FLORAL,MUGUET,POWDERY
 
 
Synonyms   Articles   Notes   Search   Top
Cosmetic Information:
CosIng: cosmetic data
Cosmetic Uses: perfuming agents
Synonyms   Articles   Notes   Search   Top
Suppliers:
Augustus Oils
Lilial
Services
BASF
Lysmeral Extra®
Odor: Floral, muguet, powdery
BOC Sciences
For experimental / research use only.
3-(4-tert-Butylphenyl)-2-methylpropionaldehyde
Creatingperfume.com
Lilestralis / Lysmeral
Odor: Fresh, light, green floral, reminiscent of lily
ECSA Chemicals
Lilial
Company Profile
Emerald Kalama Chemical
Kalama® Lilestralis® Pure
Odor: Fresh, light, green, floral, lily
Ernesto Ventós
LILY ALDEHYDE EXTRA
Odor: FRESH, LIGHT, FLORAL,MUGUET,POWDERY
Ernesto Ventós
LYSMERAL EXTRA BASF
Odor: FRESH, LIGHT, FLORAL,MUGUET,POWDERY
Ernesto Ventós
LYSMERAL/LYRAL SUBSTITUTE-LILIAL BASE
Odor: FRESH,LIGHT,FLORAL,MUGUET,POWDERY
Global Essence
Lilial
Indenta Group
Lilyal
Indukern F&F
LILESTRALIS PURE
Odor: FRESH, GREEN, FLORAL, LILAC
Indukern F&F
LILIALDEHYDE
Odor: FRESH, GREEN, FLORAL, LILAC
Indukern F&F
MEFLORAL
Odor: FRESH, FLORAL, GREEN
Inoue Perfumery
LILY ALDEHYDE PURE
Lluch Essence
LILIAL
Moellhausen
ALDEHYDE MBDC PURE
Pell Wall Perfumes
Lilial
Penta International
LILIAL REGULAR
Penta International
LILIAL
PerfumersWorld
Lilial
Odor: fresh light green floral lily notes muguet lindenblossom
Perfumery Laboratory
LILIAL
Odor: Sweet, floral fragrance of the lily of the valley
Phoenix Aromas & Essential Oils
Lilial
Prinova
Lilialdehyde
Prodasynth
LILIAL
(> 99%
Odor: FRESH, LIGHT, FLORAL,MUGUET,POWDERY
Santa Cruz Biotechnology
For experimental / research use only.
2-(4-tert-Butylbenzyl)propionaldehyde ≥95%
Sigma-Aldrich
For experimental / research use only.
2-(4-tert-Butylbenzyl)propionaldehyde analytical standard
SRS Aromatics
LILIALDEHYDE
Taytonn
Lilestralis®
Odor: Floral, Fresh, Green
TCI AMERICA
For experimental / research use only.
3-(4-tert-Butylphenyl)isobutyraldehyde >96.0%(GC)
The Good Scents Company
lilyall
Odor: floral muguet watery green powdery cumin
The John D. Walsh Company
Lilestralis
The John D. Walsh Company
Mefloral
The Lermond Company
LILIAL
The Perfumers Apprentice
Lilial a.k.a Lilestralis
Odor: fresh slightly green lily watery
Vigon International
Lysmeral Extra (Lilial)
Synonyms   Articles   Notes   Search   Top
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.
R 43 - May cause sensitisation by skin contact.
S 02 - Keep out of the reach of children.
S 24/25 - Avoid contact with skin and eyes.
S 26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S 37 - Wear suitable gloves.
 
Hazards identification
 
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
Acute toxicity, Oral (Category 4), H302
Skin irritation (Category 2), H315
Skin sensitisation (Category 1), H317
Reproductive toxicity (Category 2), H361
Acute aquatic toxicity (Category 2), H401
Chronic aquatic toxicity (Category 2), H411
GHS Label elements, including precautionary statements
 
Pictogramhealth-hazard.jpgexclamation-mark.jpgenvironment.jpg
 
Signal word Warning
Hazard statement(s)
H302 - Harmful if swallowed
H315 - Causes skin irritation
H317 - May cause an allergic skin reaction
H361 - Suspected of damaging fertility or the unborn child
H401 - Toxic to aquatic life
H411 - Toxic to aquatic life with long lasting effects
Precautionary statement(s)
P201 - Obtain special instructions before use.
P202 - Do not handle until all safety precautions have been read and understood.
P261 - Avoid breathing dust/fume/gas/mist/vapours/spray.
P264 - Wash skin thouroughly after handling.
P270 - Do not eat, drink or smoke when using this product.
P272 - Contaminated work clothing should not be allowed out of the workplace.
P273 - Avoid release to the environment.
P280 - Wear protective gloves/protective clothing/eye protection/face protection.
P281 - Use personal protective equipment as required.
P301 + P312 - IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.
P302 + P352 - IF ON SKIN: wash with plenty of soap and water.
P308 + P313 - IF exposed or concerned: Get medical advice/attention.
P330 - Rinse mouth.
P333 + P313 - IF SKIN irritation or rash occurs: Get medical advice/attention.
P362 - Take off contaminated clothing and wash before reuse.
P391 - Collect spillage. Hazardous to the aquatic environment
P405 - Store locked up.
P501 - Dispose of contents/container in accordance with local/regional/national/international regulations.
Human Experience:
4 % solution: no irritation or sensitization.
Oral/Parenteral Toxicity:
oral-rat LD50  1390 mg/kg
BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY) LUNGS, THORAX, OR RESPIRATION: DYSPNEA
National Technical Information Service. Vol. OTS0535449

intraperitoneal-mouse LD50  700 mg/kg
National Technical Information Service. Vol. OTS0535449

Dermal Toxicity:
skin-rabbit LD50 > 5000 mg/kg
National Technical Information Service. Vol. OTS0535449

Inhalation Toxicity:
Not determined
Synonyms   Articles   Notes   Search   Top
Safety in Use Information:
Category: fragrance agents
IFRA Code of Practice Notification of the 49th Amendment to the IFRA Code of Practice
IFRA Critical Effect: Dermal sensitization and systemic toxicity
contains the following IFRA (Annex) restricted components: (non-analysis max. level reference only)
lilyall / methyl anthranilate schiff's base Max. Found: 60.60 % and Reason: Sensitization
IFRA: View 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
Prohibited %
Category 2: Products applied to the axillae
0.09 %
Category 3: Products applied to the face/body using fingertips
0.04 %
Category 4: Products related to fine fragrance
1.40 %
 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
0.06 %
Category 5B: Face moisturizer products applied to the face using the hands (palms), primarily leave-on
0.05 %
Category 5C: Hand cream products applied to the hands using the hands (palms), primarily leave-on
0.05 %
Category 5D: Baby Creams, baby Oils and baby talc
0.017 %
Category 6: Products with oral and lip exposure
Prohibited %
 Category 7: Products applied to the hair with some hand contact
Category 7A: Rinse-off products applied to the hair with some hand contact
0.04 %
Category 7B: Leave-on products applied to the hair with some hand contact
0.04 %
Category 8: Products with significant anogenital exposure
0.017 %
Category 9: Products with body and hand exposure, primarily rinse off
0.10 %
 Category 10: Household care products with mostly hand contact
Category 10A: Household care excluding aerosol products (excluding aerosol/spray products)
0.10 %
Category 10B: Household aerosol/spray products
0.63 %
 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
0.017 %
Category 11B: Products with intended skin contact but minimal transfer of fragrance to skin from inert substrate with potential UV exposure
0.017 %
Category 12: Products not intended for direct skin contact, minimal or insignificant transfer to skin
16.00 %
 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.

 
Recommendation for lilyall flavor usage levels up to:
 not for flavor use.
Synonyms   Articles   Notes   Search   Top
Safety References:
EPI System: View
Cancer Citations: Search
Toxicology Citations: Search
EPA Substance Registry Services (TSCA): 80-54-6
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 6652
National Institute of Allergy and Infectious Diseases: Data
SCCNFP: opinion
WISER: UN 3082
WGK Germany: 3
 3-(4-tert-butylphenyl)butanal
Chemidplus: 0000080546
RTECS: MW4895000 for cas# 80-54-6
Synonyms   Articles   Notes   Search   Top
References:
Leffingwell: Chirality or Article
 3-(4-tert-butylphenyl)butanal
NIST Chemistry WebBook: Search Inchi
Canada Domestic Sub. List: 80-54-6
Pubchem (cid): 6652
Pubchem (sid): 134972321
Synonyms   Articles   Notes   Search   Top
Other Information:
(IUPAC): Atomic Weights of the Elements 2009
(IUPAC): Atomic Weights of the Elements 2009 (pdf)
Videos: The Periodic Table of Videos
tgsc: Atomic Weights use for this web site
(IUPAC): Periodic Table of the Elements
HMDB (The Human Metabolome Database): Search
Export Tariff Code: 2912.49.2600
ChemSpider: View
Wikipedia: View
RSC Learn Chemistry: View
Synonyms   Articles   Notes   Search   Top
Potential Blenders and core components note
 
For Odor
aldehydic
 adoxal (Givaudan)FL/FR
 citronellyl oxyacetaldehydeFL/FR
 citrus carbaldehydeFR
 decanal (aldehyde C-10)FL/FR
9-decenalFL/FR
 dodecanal (aldehyde C-12 lauric)FL/FR
 lily pentanalFR
 nonanal (aldehyde C-9)FL/FR
10-undecenal (aldehyde C-11 undecylenic)FL/FR
animal
para-cresyl isobutyrateFL/FR
anisic
para-anisaldehydeFL/FR
balsamic
 amyris wood oilFL/FR
siam benzoin resinoidFL/FR
 benzyl salicylateFL/FR
isobutyl cinnamateFL/FR
 cinnamyl alcoholFL/FR
(E)-cinnamyl alcoholFL/FR
 clover nitrileFR
 ethyl cinnamateFL/FR
 fir balsam absoluteFR
 linalyl cinnamateFL/FR
3-phenyl propyl alcoholFL/FR
berry
 raspberry ketoneFL/FR
 raspberry ketone acetateFL/FR
 raspberry ketone methyl etherFL/FR
citrus
 benzyl anthranilateFR
 citrus ocimenolFR
isodecyl acetateFR
 lime oil distilled mexicoFL/FR
 methyl indole-1-carboxylateFR
 myrmac aldehydeFR
 tetrahydromyrcenolFR
fatty
 decanolFL/FR
floral
 aeolanthus graveolens oilFR
alpha-amyl cinnamaldehydeFL/FR
alpha-amyl cinnamaldehyde dimethyl acetalFL/FR
isoamyl salicylateFL/FR
 bois de rose oil brazilFL/FR
alpha-butyl cinnamaldehydeFL/FR
4-isobutyl cyclohexane propanalFR
isobutyl salicylateFL/FR
 citronellolFL/FR
 citronellyl (R)-lactateFR
 citronellyl acetateFL/FR
 citronellyl ethoxalateFR
 citrus propanolFR
 coriander seed oilFL/FR
 corps popinalFR
 cumin carbinolFR
 cuminyl acetaldehydeFL/FR
 cyclamen aldehydeFL/FR
 cyclamen homoaldehydeFR
 cyclohexyl ethyl alcoholFL/FR
 cyclohexyl propanolFR
2-decalinolFR
 dihydrojasmoneFL/FR
 dimethyl anthranilateFL/FR
 dimethyl benzyl carbinolFL/FR
 dimethyl benzyl carbinyl acetateFL/FR
2,5-dimethyl-2-indan methanolFR
4-ethyl cyclohexane propanalFR
 ethyl linalyl acetalFR
(E,E)-farnesolFL/FR
 farnesolFL/FR
 floral butanalFR
 floral pyranolFR
 floral specialtyFR
 freesia acetateFR
 gardenia oxideFR
 geraniolFL/FR
 geranyl acetateFL/FR
 ginger lily fragranceFR
 hawthorn ethanolFR
 heliotropinFL/FR
 heliotropyl acetoneFL/FR
 heliotropyl diethyl acetalFR
(Z)-4-hepten-2-yl salicylateFR
(Z)-3-hexen-1-yl salicylateFL/FR
alpha-hexyl cinnamaldehydeFL/FR
 hyacinth etherFR
 hydrangea fragranceFR
3-(4-hydroxy-4-methyl cyclohexyl) butanalFR
 hydroxycitronellalFL/FR
 hydroxycitronellal / methyl anthranilate schiff's baseFR
 hydroxycitronellal diethyl acetalFL/FR
 hydroxycitronellal dimethyl acetalFL/FR
 hydroxycitronellal distillation residue distillatesFR
 hydroxycitronellal nitrileFR
 hydroxycitronellal propylene glycol acetalFL/FR
 hydroxycitronellal residueFR
 hydroxycitronellolFL/FR
 jasimiaFR
 leerallFR
 leerall / methyl anthranilate schiff's baseFR
 lily flower absoluteFR
 lily fragranceFR
water lily fragranceFR
calla lily fragranceFR
 lily of the valley fragranceFR
 lily of the valley specialtyFR
 lilyall / methyl anthranilate schiff's baseFR
 lilyall substituteFR
 linaloolFL/FR
 linalool oxideFL/FR
 linalyl benzoateFL/FR
 lotus fragranceFR
 magnolia cyclohexanolFR
 magnolia decadienalFR
 methoxycitronellalFR
4-methyl cyclohexane propanalFR
 methyl dihydrojasmonateFL/FR
2-methyl octanalFL/FR
1-methyl-3-(2-methyl propyl) cyclohexanolFR
4-(4-methyl-4-hydroxyamyl)-delta3-cyclohexenecarboxaldehydeFR
3-methyl-6-ethyl-5-octen-1-olFR
 mimosa absolute franceFL/FR
 muguet butanalFR
 muguet butanolFR
 muguet carbaldehydeFR
 muguet carbinolFL/FR
 muguet carboxaldehydeFR
 muguet ethanolFR
 muguet nitrileFR
 muguet octadienolFR
 muguet propanolFR
 muguet shiseolFL/FR
cis-muguet shiseolFL/FR
 muguet specialtyFR
 nerolFL/FR
 nerolidolFL/FR
 neryl acetateFL/FR
 ocean propanalFL/FR
 octahydro-4,7-methano-1H-indene-5-acetaldehydeFR
 octahydro-4,7-methano-1H-indene-5-acetaldehyde + 6-methyl-octahydro-4,7-methano-indene-5-carbaldehydFR
 orchid specialtyFR
 orris pyridine 25% IPMFR
2-pentyl-2-cyclohexen-1-oneFR
 peony alcoholFR
 phenethyl alcoholFL/FR
 phenethyl phenyl acetateFL/FR
 phenethyl salicylateFL/FR
 phenyl acetaldehyde digeranyl acetalFR
 phenyl glycol diacetateFR
4-propyl cyclohexane propanalFR
 rhodinolFL/FR
 rose absolute pentanolFR
 rose butanoateFL/FR
alpha-terpinyl anthranilateFL/FR
 tetrahydrolinaloolFL/FR
(S,E)-3,7,11-trimethyldodeca-6,10-dienalFR
 verdyl acetateFR
 violet methyl carbonateFR
 ylang ylang flower oilFL/FR
 ylang ylang flower oil CO2 extractFL/FR
 ylang ylang flower oil fractionsFR
 ylang ylang flower oil IFL/FR
 ylang ylang flower oil IIFL/FR
 ylang ylang oil III fractionsFR
 ylang ylang oil replacerFR
fruity
 allyl amyl glycolateFR
 dimethyl benzyl carbinyl isobutyrateFR
 ethyl bicyclo(2.2.1)-5-heptene-2-carboxylateFL/FR
 peach pivalateFR
green
 acetaldehyde ethyl phenethyl acetalFL/FR
(Z)-3-hexen-1-olFL/FR
(Z)-3-hexen-1-yl benzoateFL/FR
2,4-ivy carbaldehydeFL/FR
(Z)-leaf acetalFL/FR
 melon nonenoateFL/FR
 phenyl acetaldehyde diethyl acetalFL/FR
 phenyl acetaldehyde dimethyl acetalFL/FR
 phenyl acetaldehyde ethylene glycol acetalFR
 violet decenolFR
 violet leaf absoluteFL/FR
hay
 hay absoluteFR
herbal
 clary sage oil franceFL/FR
 daucus carota fruit oilFL/FR
 dimethyl benzyl carbinyl formateFL/FR
 linalyl acetateFL/FR
 pine hexanolFR
marine
 marine pyridineFR
 ozone propanalFR
melon
 watermelon ketoneFR
mossy
 veramoss (IFF)FR
muguet
4-isobutyl 1-(3-methoxy-2-propen-1-yl) benzeneFR
4-ethyl 1-(3-methoxy-2-propen-1-yl) benzeneFR
4-methyl 1-(3-methoxy-2-propen-1-yl) benzeneFR
4-propyl 1-(3-methoxy-2-propen-1-yl) benzeneFR
naphthyl
beta-naphthyl ethyl etherFL/FR
powdery
para-anisyl alcoholFL/FR
spicy
isoeugenyl acetateFL/FR
terpenic
alpha-terpineolFL/FR
tonka
 tonka bean absoluteFR
vanilla
 ethyl vanillinFL/FR
 vanilla bean absolute (vanilla planifolia)FL/FR
 vanillyl acetateFL/FR
waxy
 decyl acetateFL/FR
1-dodecanolFL/FR
 ethyl laurateFL/FR
1-undecanolFL/FR
woody
 amber dioxaneFR
 cedryl methyl etherFR
 guaiacwood oilFL/FR
 hydroxycitronellal diisotridecyl acetalFR
 patchouli ethanoneFR
 santallFR
 tobacarol (IFF)FR
 woody acetateFR
(Z)-woody amyleneFR
 
For Flavor
 
No flavor group found for these
alpha-amyl cinnamaldehyde dimethyl acetalFL/FR
(E)-cinnamyl alcoholFL/FR
9-decenalFL/FR
 dimethyl benzyl carbinyl formateFL/FR
 ethyl bicyclo(2.2.1)-5-heptene-2-carboxylateFL/FR
(E,E)-farnesolFL/FR
 hydroxycitronellal propylene glycol acetalFL/FR
2-methyl octanalFL/FR
 phenyl acetaldehyde diethyl acetalFL/FR
alpha-terpinyl anthranilateFL/FR
alpha-butyl cinnamaldehydeFL/FR
aldehydic
 nonanal (aldehyde C-9)FL/FR
1-undecanolFL/FR
aromatic
para-cresyl isobutyrateFL/FR
balsamic
siam benzoin resinoidFL/FR
 benzyl salicylateFL/FR
isobutyl cinnamateFL/FR
 ethyl cinnamateFL/FR
berry
 heliotropyl acetoneFL/FR
 raspberry ketoneFL/FR
 raspberry ketone acetateFL/FR
 raspberry ketone methyl etherFL/FR
cherry
 heliotropinFL/FR
citrus
 citronellyl oxyacetaldehydeFL/FR
 lime oil distilled mexicoFL/FR
 linaloolFL/FR
 nerolFL/FR
alpha-terpineolFL/FR
cooling
isobutyl salicylateFL/FR
creamy
para-anisaldehydeFL/FR
fatty
(Z)-3-hexen-1-yl benzoateFL/FR
10-undecenal (aldehyde C-11 undecylenic)FL/FR
floral
 bois de rose oil brazilFL/FR
 citronellolFL/FR
 citronellyl acetateFL/FR
 dihydrojasmoneFL/FR
 dimethyl benzyl carbinyl acetateFL/FR
 farnesolFL/FR
 geraniolFL/FR
 linalyl acetateFL/FR
 methyl dihydrojasmonateFL/FR
 muguet carbinolFL/FR
 muguet shiseolFL/FR
cis-muguet shiseolFL/FR
 neryl acetateFL/FR
 ocean propanalFL/FR
 phenethyl alcoholFL/FR
 rhodinolFL/FR
 tetrahydrolinaloolFL/FR
 ylang ylang flower oilFL/FR
 ylang ylang flower oil CO2 extractFL/FR
 ylang ylang flower oil IFL/FR
 ylang ylang flower oil IIFL/FR
fruity
para-anisyl alcoholFL/FR
 dimethyl anthranilateFL/FR
 linalyl benzoateFL/FR
 linalyl cinnamateFL/FR
 rose butanoateFL/FR
green
 acetaldehyde ethyl phenethyl acetalFL/FR
isoamyl salicylateFL/FR
 cinnamyl alcoholFL/FR
 cuminyl acetaldehydeFL/FR
 cyclamen aldehydeFL/FR
 cyclohexyl ethyl alcoholFL/FR
 geranyl acetateFL/FR
(Z)-3-hexen-1-olFL/FR
(Z)-3-hexen-1-yl salicylateFL/FR
2,4-ivy carbaldehydeFL/FR
(Z)-leaf acetalFL/FR
 linalool oxideFL/FR
 melon nonenoateFL/FR
 nerolidolFL/FR
 phenyl acetaldehyde dimethyl acetalFL/FR
 violet leaf absoluteFL/FR
herbal
 clary sage oil franceFL/FR
 coriander seed oilFL/FR
 daucus carota fruit oilFL/FR
honey
 phenethyl phenyl acetateFL/FR
medicinal
 dimethyl benzyl carbinolFL/FR
 phenethyl salicylateFL/FR
melon
 hydroxycitronellal diethyl acetalFL/FR
powdery
 hydroxycitronellolFL/FR
beta-naphthyl ethyl etherFL/FR
soapy
 dodecanal (aldehyde C-12 lauric)FL/FR
1-dodecanolFL/FR
spicy
isoeugenyl acetateFL/FR
3-phenyl propyl alcoholFL/FR
tropical
alpha-amyl cinnamaldehydeFL/FR
vanilla
 ethyl vanillinFL/FR
 vanilla bean absolute (vanilla planifolia)FL/FR
 vanillyl acetateFL/FR
waxy
 adoxal (Givaudan)FL/FR
 decanal (aldehyde C-10)FL/FR
 decanolFL/FR
 decyl acetateFL/FR
 ethyl laurateFL/FR
alpha-hexyl cinnamaldehydeFL/FR
 hydroxycitronellalFL/FR
 hydroxycitronellal dimethyl acetalFL/FR
 mimosa absolute franceFL/FR
woody
 amyris wood oilFL/FR
 guaiacwood oilFL/FR
 
Synonyms   Articles   Notes   Search   Top
Potential Uses:
 alliage 
 anais anais 
 azzaro 
 blue mistFR
 bouquetFR
 bubble gumFR
 calyx 
 cedarFR
 charlie 
 cherry blossomFR
 citrusFR
 clean 
 clean linenFR
 coconut tropical coconutFR
 country meadowFR
 cyclamenFR
 devin 
 estee 
 eternity 
 fernFR
 floralFR
 gardeniaFR
 grapefruitFR
 greenFR
 halston 
 herbalFR
 honeysuckleFR
 j' ai ose 
 lilacFR
 lilyFR
 lily of the valleyFR
 linden flowerFR
 lotusFR
 marbert man 
 mintFR
 muskFR
 new carFR
 paco rabanne 
 pineFR
 potpourriFR
 pour homme 
 rainFR
 roseFR
 sandalwoodFR
 sea breezeFR
 spring rainFR
 tide 
 turbulences 
 woodyFR
Synonyms   Articles   Notes   Search   Top
Occurrence (nature, food, other): note
 not found in nature
Synonyms   Articles   Notes   Search   Top
Synonyms:
 aldehyde MBDC
 aldehyde MBDC pure
2-(4-tert-butyl benzyl) propionaldehyde
 butyl phenyl methyl propional
p-tert-butyl-a-methyldihydrocinnamic aldehyde
p-tert-butyl-a-methylhydrocinnamaldehyde
p-tert-butyl-a-methylhydrocinnamic aldehyde
p-tert-butyl-alpha-methyl dihydrocinnamaldehyde
para-tert-butyl-alpha-methyl dihydrocinnamaldehyde
meta-tert-butyl-alpha-methyl dihydrocinnamic aldehyde
p-tert-butyl-alpha-methyl dihydrocinnamic aldehyde
para-tert-butyl-alpha-methyl dihydrocinnamic aldehyde
p-tert-butyl-alpha-methyl hydrocinnamaldehyde
para-tert-butyl-alpha-methyl hydrocinnamaldehyde
p-tert-butyl-alpha-methyl hydrocinnamic aldehyde
para-tert-butyl-alpha-methyl hydrocinnamic aldehyde
m-tert-butyl-alpha-methyldihydrocinnamic aldehyde
2-(4-tert-butylbenzyl)propionaldehyde
3-(4-tert-butylphenyl)butanal
 butylphenylmethylpropional
4-(1,1-dimethyl ethyl)-alpha-methyl benzene propanal
4-(1,1-dimethylethyl)-alpha-methylbenzenepropanal
 hydrocinnamaldehyde, p-tert-butyl-a-methyl-
 lilestralis
 lilestralis pure
 lilial
 lilialdehyde
 liligul N 743 CLP
 lilyall
 lysmeral
 lysmeral extra
 mefloral
3-[4-(2-methyl-2-propanyl)phenyl]butanal
alpha-methyl-beta-(p-tert-butylphenyl)propionaldehyde
alpha-methyl-beta-(para-tert-butyl phenyl) propionaldehyde
a-methyl-p-(tert-butyl)hydrocinnamaldehyde
alpha-methyl-p-(tert-butyl)hydrocinnamaldehyde
alpha-methyl-para-(tert-butyl) hydrocinnamaldehyde
Synonyms   Articles   Notes   Search   Top
Articles:
US Patents: 4,778,934 - Process for the manufacture of p-tert-butyl-.alpha.-methylhydrocinnamaldehyde
PubMed: Genotoxicity assessment of some cosmetic and food additives.
US Patents: 4,568,772 - Process for the preparation of p-t-butyl-.alpha.-methyldihydrocinnamaldehyde
PubMed: Vocational interests of intellectually gifted and highly achieving young adults.
US Patents: 4,568,772 - Process for the preparation of p-t-butyl-.alpha.-methyldihydrocinnamaldehyde
PubMed: Two fragrance chemicals may act as toxicants via TRPA1 stimulation rather than via direct mitochondrial action.
PubMed: Occurrences and potential risks of 16 fragrances in five German sewage treatment plants and their receiving waters.
PubMed: Fragrance chemicals lyral and lilial decrease viability of HaCat cells' by increasing free radical production and lowering intracellular ATP level: protection by antioxidants.
PubMed: Phosphoinositide 3-kinase-dependent antagonism in mammalian olfactory receptor neurons.
PubMed: Olfactory sensitivity for sperm-attractant aromatic aldehydes: a comparative study in human subjects and spider monkeys.
PubMed: Sorbent trapping solid-phase microextraction of fragrance allergens in indoor air.
PubMed: Determination of suspected allergens in cosmetic products by headspace-programmed temperature vaporization-fast gas chromatography-quadrupole mass spectrometry.
PubMed: Bioreduction of alpha-methylcinnamaldehyde derivatives: chemo-enzymatic asymmetric synthesis of Lilial and Helional.
PubMed: Quantitative determination of some volatile suspected allergens in cosmetic creams spread on skin by direct contact sorptive tape extraction-gas chromatography-mass spectrometry.
PubMed: Large-scale production and study of a synthetic G protein-coupled receptor: human olfactory receptor 17-4.
PubMed: Oestrogenic activity of benzyl salicylate, benzyl benzoate and butylphenylmethylpropional (Lilial) in MCF7 human breast cancer cells in vitro.
PubMed: Polyvalent type IV sensitizations to multiple fragrances and a skin protection cream in a metal worker.
PubMed: HMOX1 and NQO1 genes are upregulated in response to contact sensitizers in dendritic cells and THP-1 cell line: role of the Keap1/Nrf2 pathway.
PubMed: Odorant design based on the carbon/silicon switch strategy.
PubMed: Sensitization to 26 fragrances to be labelled according to current European regulation. Results of the IVDK and review of the literature.
PubMed: Fragrance ingredient labelling in products on sale in the U.K.
PubMed: High-performance liquid chromatographic method for the simultaneous determination of 24 fragrance allergens to study scented products.
PubMed: Prediction of perception: probing the hOR17-4 olfactory receptor model with silicon analogues of bourgeonal and lilial.
PubMed: Cross-adaptation between olfactory responses induced by two subgroups of odorant molecules.
PubMed: A psychophysical study of the relationship between temporal processing in odor mixtures and transduction pathways.
PubMed: Identification of Lilial as a fragrance sensitizer in a perfume by bioassay-guided chemical fractionation and structure-activity relationships.
PubMed: Blocking adenylyl cyclase inhibits olfactory generator currents induced by "IP(3)-odors".
PubMed: Regulation of cutaneous allergic reaction by odorant inhalation.
PubMed: Responses to putative second messengers and odorants in water nose olfactory neurons of Xenopus laevis.
PubMed: Subtypes of odorant-binding proteins--heterologous expression and ligand binding.
PubMed: Odorants selectively activate distinct G protein subtypes in olfactory cilia.
PubMed: Ca2+ and Cl(-)-dependence of the turtle olfactory response to odorants and forskolin.
PubMed: Chemosensitivity of the osphradium of the pond snail Lymnaea stagnalis
PubMed: Odor-induced phosphorylation of olfactory cilia proteins.
PubMed: Allergic contact dermatitis to the fragrance material lilial.
Synonyms   Articles   Notes   Search   Top
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