2-para-cresyl oxyethyl acetate
2-(p-tolyloxy)ethanol acetate
 
Notes:
None found
  • Tadimety Aromatics
    • Tadimety Aromatics Private Limited
      A Global Brand
      Manufacturing more than 70+ speciality aroma chemicals.
      Tadimety Aromatics Pvt Ltd was founded in the year 1996. Madhu Chakrapani Rao with a couple of like-minded people began the operation of the company in a small facility totalling 2000 sq ft. Like most start-up companies Tadimety Aromatics underwent difficult times during first few years. The company ability to overcome initial obstacles and its current success can be attributed in part to Madhu Chakrapani Rao’s early decision to focus on core organic chemistry and manufacture speciality aroma chemicals for customers specific requirements.
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      Product(s):
      TT0698 Grandiflor
       
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    • TCI AMERICA
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      Tokyo Chemical Industry Co., Ltd. (TCI) is a leading worldwide manufacturer of specialty organic chemicals founded in 1946. TCI provides organic laboratory chemicals as well as pharmaceutical, cosmetic and functional materials. More than 70 years of synthesis experience and multi-purpose plants enable TCI to offer more than 30,000 products as well as custom synthesis.
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      Product(s):
      A0819 4-(2-acetoxyethoxy)toluene >98.0%(GC)
       
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CAS Number: 6807-11-0Picture of molecule3D/inchi
ECHA EINECS - REACH Pre-Reg: 229-881-1
FDA UNII: JE83E4XFCE
Nikkaji Web: J149.775H
MDL: MFCD00059337
XlogP3-AA: 2.10 (est)
Molecular Weight: 194.23018000
Formula: C11 H14 O3
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
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Physical Properties:
Assay: 95.00 to 100.00 % 
Food Chemicals Codex Listed: No
Boiling Point: 266.00 to  267.00 °C. @ 760.00 mm Hg (est)
Vapor Pressure: 0.008000 mmHg @ 25.00 °C. (est)
Flash Point: 223.00 °F. TCC ( 106.20 °C. ) (est)
logP (o/w): 2.191 (est)
Soluble in:
 alcohol
 water, 253.9 mg/L @ 25 °C (est)
Insoluble in:
 water
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Organoleptic Properties:
 
Odor Type: floral
 
Odor Strength: medium
 
 floral  jasmin  gardenia  fruity  balsamic  
Odor Description:
at 100.00 %. 
floral jasmin gardenia fruity balsamic
 
Odor and/or flavor descriptions from others (if found).
 
Tadimety Aromatics
Grandiflor
Odor Description: Floral, Reminiscent of Grandiflorum, Fruity, balsamic
 
 
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Cosmetic Information:
CosIng: cosmetic data
Cosmetic Uses: perfuming agents
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Suppliers:
Tadimety Aromatics
Grandiflor
Odor: Floral, Reminiscent of Grandiflorum, Fruity, balsamic
TCI AMERICA
For experimental / research use only.
4-(2-acetoxyethoxy)toluene >98.0%(GC)
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Safety Information:
 
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: fragrance agents
IFRA Code of Practice Notification of the 49th Amendment to the IFRA Code of Practice
 
Recommendation for 2-para-cresyl oxyethyl acetate flavor usage levels up to:
 not for flavor use.
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Safety References:
EPI System: View
AIDS Citations: Search
Cancer Citations: Search
Toxicology Citations: Search
EPA Substance Registry Services (TSCA): 6807-11-0
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 81258
National Institute of Allergy and Infectious Diseases: Data
 2-(4-methylphenoxy)ethyl acetate
Chemidplus: 0006807110
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References:
 2-(4-methylphenoxy)ethyl acetate
NIST Chemistry WebBook: Search Inchi
Canada Domestic Sub. List: 6807-11-0
Pubchem (cid): 81258
Pubchem (sid): 135038543
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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
HMDB (The Human Metabolome Database): Search
Export Tariff Code: 2914.50.3000
ChemSpider: View
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Potential Blenders and core components note
 
For Odor
aromatic
(4E,9Z)-13-methyloxacyclopentadeca-4,9-dien-2-oneFR
balsamic
isoamyl benzoateFL/FR
 benzyl cinnamateFL/FR
isobutyl cinnamateFL/FR
(E)-cinnamyl butyrateFL/FR
 cinnamyl cinnamateFL/FR
 cinnamyl formateFL/FR
 pine needle absoluteFL/FR
 prenyl benzoateFL/FR
isopropyl cinnamateFL/FR
 terpinyl butyrateFL/FR
floral
alpha-amyl cinnamaldehyde diethyl acetalFR
alpha-amyl cinnamaldehyde dimethyl acetalFL/FR
alpha-amyl cinnamyl acetateFL/FR
 benzyl acetoneFL/FR
 benzyl alcoholFL/FR
 benzyl formateFL/FR
 benzyl isobutyrateFL/FR
 benzyl phenyl acetateFL/FR
 dihydrojasmoneFL/FR
 dimethyl benzyl carbinyl propionateFR
 frangipani specialtyFR
 gardenia oxideFR
 gelsone (IFF)FL/FR
 geranyl phenyl acetateFL/FR
 honeysuckle absoluteFR
 jasmin lactone (IFF)FL/FR
 jasmin pyranolFR
 kewada oil replacerFR
 kewda fragranceFR
 methyl jasmonateFL/FR
 methyl phenoxyethanolFR
2-methyl-4-phenyl-1,3-dioxolaneFR
 nyctanthes arbor-tristis flower oilFR
2-pentadecanoneFL/FR
2-pentyl cyclopentan-1-olFR
4-phenyl-3-buten-2-olFL/FR
 pittosporum specialtyFR
 wallflower absoluteFR
 ylang ylang oil III fractionsFR
fruity
 allyl (E)-cinnamateFL/FR
 allyl cinnamateFL/FR
 balsam specialtyFR
(E)-cinnamyl propionateFL/FR
 peach nitrileFR
3-phenyl propyl isobutyrateFL/FR
(R)-styralyl acetateFL/FR
green
 benzyl hexanoateFL/FR
 chrysanthemum oxideFL/FR
 hexyl (Z)-tiglateFL/FR
 picea glauca leaf absoluteFR
tobacco
 honey absoluteFL/FR
waxy
 phytyl acetateFL/FR
woody
 callitris columellaris wood oil australiaFR
 callitris intratropica wood oil australiaFR
 santalyl butyrateFL/FR
 
For Flavor
 
No flavor group found for these
 allyl (E)-cinnamateFL/FR
 allyl cinnamateFL/FR
alpha-amyl cinnamaldehyde dimethyl acetalFL/FR
 benzyl hexanoateFL/FR
(E)-cinnamyl butyrateFL/FR
(E)-cinnamyl propionateFL/FR
 hexyl (Z)-tiglateFL/FR
 jasmin lactone (IFF)FL/FR
 phytyl acetateFL/FR
 pine needle absoluteFL/FR
 prenyl benzoateFL/FR
 santalyl butyrateFL/FR
(R)-styralyl acetateFL/FR
balsamic
isobutyl cinnamateFL/FR
isopropyl cinnamateFL/FR
earthy
alpha-amyl cinnamyl acetateFL/FR
fatty
2-pentadecanoneFL/FR
floral
 dihydrojasmoneFL/FR
 geranyl phenyl acetateFL/FR
 methyl jasmonateFL/FR
 terpinyl butyrateFL/FR
fruity
isoamyl benzoateFL/FR
 benzyl acetoneFL/FR
 benzyl alcoholFL/FR
 benzyl formateFL/FR
 benzyl isobutyrateFL/FR
3-phenyl propyl isobutyrateFL/FR
green
 chrysanthemum oxideFL/FR
 gelsone (IFF)FL/FR
honey
 benzyl phenyl acetateFL/FR
 honey absoluteFL/FR
spicy
 benzyl cinnamateFL/FR
 cinnamyl cinnamateFL/FR
 cinnamyl formateFL/FR
waxy
4-phenyl-3-buten-2-olFL/FR
 
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Potential Uses:
None Found
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Occurrence (nature, food, other): note
 not found in nature
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Synonyms:
4-(2-acetoxyethoxy)toluene
p-(2-acetoxyethoxy)toluene
2-p-cresyl oxyethyl acetate
 ethanol, 2-(4-methylphenoxy)-, acetate
 grandiflor (Tadimety)
2-(4-methylphenoxy)ethyl acetate
2-(p-tolyl oxy)ethanol acetate
2-(para-tolyl oxy)ethanol acetate
2-(p-tolyloxy)ethanol acetate
2-(p-tolyloxy)ethyl acetate
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