ortho-tolualdehyde
o-tolualdehyde
 
Notes:
Component of FEMA 3068. Flavouring ingredient (see further under 4-Methylbenzaldehyde BHW21-S)
  • BOC Sciences
    • BOC Sciences
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      529-20-4 o-Tolualdehyde Practical
       
  • Jiangyin Healthway
    • Jiangyin Healthway International Trade Co., Ltd
      Independent Ingredients Supplier
      We provide custom synthesis and contract manufacturing from milligrams to metric tonnes.
      Jiangyin Healthway International Trade Co., Ltd is a professional company, main engaged in manufacturing and exporting aroma chemicals ,food additives , cosmetic ingredient ,pharmaceutical intermediates & other fine chemicals; especially on aroma chemicals , as the major manufacturer of heterocyclic and sulphur aroma compounds , we are the leading independent ingredients supplier to the flavour and fragrance industries in China, can offer hundreds of different high quality aroma chemicals.
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      Product(s):
      HLO266 o-Tolualdehyde
       
  • Penta International
    • Penta International Corporation
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      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):
      20-54200 O-TOLUALDEHYDE
       
  • Sigma-Aldrich
  • TCI AMERICA
    • 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):
      T0566 o-Tolualdehyde >98.0%(GC)
       
Synonyms   Articles   Notes   Search
CAS Number: 529-20-4Picture of molecule3D/inchi
ECHA EINECS - REACH Pre-Reg: 208-452-2
FDA UNII: Q7E5H6W6BG
Nikkaji Web: J6.680J
Beilstein Number: 0605841
MDL: MFCD00003338
CoE Number: 115
XlogP3: 2.10 (est)
Molecular Weight: 120.15096000
Formula: C8 H8 O
BioActivity Summary: listing
NMR Predictor: Predict (works with chrome or firefox)
Category: flavor and fragrance agents
 
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Google Scholar: Search
Google Books: Search
Google Scholar: with word "volatile"Search
Google Scholar: with word "flavor"Search
Google Scholar: with word "odor"Search
Perfumer and Flavorist: Search
Google Patents: Search
US Patents: Search
EU Patents: Search
Pubchem Patents: Search
PubMed: Search
NCBI: Search
DG SANTE Food Flavourings: 05.026  o-tolualdehyde
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Physical Properties:
Appearance: colorless to pale yellow clear liquid (est)
Assay: 97.00 to 100.00 % 
Food Chemicals Codex Listed: No
Specific Gravity: 1.01300 to 1.02900 @  25.00 °C.
Pounds per Gallon - (est).: 8.429 to  8.562
Refractive Index: 1.54000 to 1.54700 @  20.00 °C.
Boiling Point: 200.00 to  201.00 °C. @ 760.00 mm Hg
Vapor Pressure: 0.397000 mmHg @ 25.00 °C. (est)
Flash Point: 171.00 °F. TCC ( 77.22 °C. )
logP (o/w): 2.260
Soluble in:
 alcohol
 water, 1178 mg/L @ 25 °C (est)
Insoluble in:
 water
Similar Items: note
meta-tolualdehyde
para-tolualdehyde
tolualdehydes (mixed o/m/p)
Synonyms   Articles   Notes   Search   Top
Organoleptic Properties:
Odor Description:
at 1.00 % in dipropylene glycol. 
cherry
 
Odor and/or flavor descriptions from others (if found).
 
 
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Cosmetic Information:
CosIng: cosmetic data
Cosmetic Uses: perfuming agents
Synonyms   Articles   Notes   Search   Top
Suppliers:
BOC Sciences
For experimental / research use only.
o-Tolualdehyde Practical
EMD Millipore
For experimental / research use only.
2-Methylbenzaldehyde
Jiangyin Healthway
o-Tolualdehyde
New functional food ingredients
Penta International
O-TOLUALDEHYDE
Santa Cruz Biotechnology
For experimental / research use only.
o-Tolualdehyde
Sigma-Aldrich
o-Tolualdehyde, ≥96.5%, FG
Certified Food Grade Products
TCI AMERICA
For experimental / research use only.
o-Tolualdehyde >98.0%(GC)
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Safety Information:
Preferred SDS: View
European information :
Most important hazard(s):
Xn - Harmful.
R 22 - Harmful if swallowed.
R 37/38 - Irritating to respiratory system and skin.
R 41 - Risk of serious damage to eyes.
S 02 - Keep out of the reach of children.
S 20/21 - When using do not eat, drink or smoke.
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 37/39 - Wear suitable gloves and eye/face protection.
 
Hazards identification
 
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
None found.
GHS Label elements, including precautionary statements
 
Pictogram
 
Hazard statement(s)
None found.
Precautionary statement(s)
None found.
Oral/Parenteral Toxicity:
Not determined
Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined
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Safety in Use Information:
Category: flavor and fragrance agents
RIFM Fragrance Material Safety Assessment: Search
IFRA Code of Practice Notification of the 49th Amendment to the IFRA Code of Practice
IFRA Critical Effect: Dermal 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
0.085 %
Category 2: Products applied to the axillae
0.025 %
Category 3: Products applied to the face/body using fingertips
0.51 %
Category 4: Products related to fine fragrance
0.47 %
 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
0.12 %
Category 5B: Face moisturizer products applied to the face using the hands (palms), primarily leave-on
0.12 %
Category 5C: Hand cream products applied to the hands using the hands (palms), primarily leave-on
0.12 %
Category 5D: Baby Creams, baby Oils and baby talc
0.12 %
Category 6: Products with oral and lip exposure
0.28 %
 Category 7: Products applied to the hair with some hand contact
Category 7A: Rinse-off products applied to the hair with some hand contact
0.96 %
Category 7B: Leave-on products applied to the hair with some hand contact
0.96 %
Category 8: Products with significant anogenital exposure
0.050 %
Category 9: Products with body and hand exposure, primarily rinse off
0.92 %
 Category 10: Household care products with mostly hand contact
Category 10A: Household care excluding aerosol products (excluding aerosol/spray products)
3.30 %
Category 10B: Household aerosol/spray products
3.30 %
 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
1.80 %
Category 11B: Products with intended skin contact but minimal transfer of fragrance to skin from inert substrate with potential UV exposure
1.80 %
Category 12: Products not intended for direct skin contact, minimal or insignificant transfer to skin
No Restriction
 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): 1.00 (μg/capita/day)
Modified Theoretical Added Maximum Daily Intake (mTAMDI): 9100 (μg/person/day)
Threshold of Concern:1800 (μg/person/day)
Structure Class: I
 
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): 15.0300017.74000
Fats and oils, and fat emulsions (type water-in-oil) (02.0): --
Edible ices, including sherbet and sorbet (03.0): --
Processed fruit (04.1): --
Processed vegetables (incl. mushrooms & fungi, roots & tubers, pulses and legumes), and nuts & seeds (04.2): --
Confectionery (05.0): 56.26000111.20000
Chewing gum (05.0): --
Cereals and cereal products, incl. flours & starches from roots & tubers, pulses & legumes, excluding bakery (06.0): --
Bakery wares (07.0): 25.8200033.56000
Meat and meat products, including poultry and game (08.0): --
Fish and fish products, including molluscs, crustaceans and echinoderms (MCE) (09.0): --
Eggs and egg products (10.0): --
Sweeteners, including honey (11.0): --
Salts, spices, soups, sauces, salads, protein products, etc. (12.0): --
Foodstuffs intended for particular nutritional uses (13.0): --
Non-alcoholic ("soft") beverages, excl. dairy products (14.1): 9.9100013.29000
Alcoholic beverages, incl. alcohol-free and low-alcoholic counterparts (14.2): 6.2300012.70000
Ready-to-eat savouries (15.0): --
Composite foods (e.g. casseroles, meat pies, mincemeat) - foods that could not be placed in categories 01.0 - 15.0 (16.0): --
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Safety References:
Flavor & Extract Manufacturers Association (FEMA) reference(s):
The FEMA GRAS assessment of benzyl derivatives used as flavor ingredients. View pdf
European Food Safety Athority(EFSA): Flavor usage levels; Subacute, Subchronic, Chronic and Carcinogenicity Studies; Developmental / Reproductive Toxicity Studies; Genotoxicity Studies...
European Food Safety Authority (EFSA) reference(s):
Scientific Opinion on Flavouring Group Evaluation 20, Revision 4 (FGE.20Rev4): Benzyl alcohols, benzaldehydes, a related acetal, benzoic acids, and related esters from chemical groups 23 and 30
View page or View pdf
EPI System: View
Chemical Carcinogenesis Research Information System: Search
Toxicology Citations: Search
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 10722
National Institute of Allergy and Infectious Diseases: Data
WGK Germany: 3
 2-methylbenzaldehyde
Chemidplus: 0000529204
EPA/NOAA CAMEO: hazardous materials
Synonyms   Articles   Notes   Search   Top
References:
 2-methylbenzaldehyde
NIST Chemistry WebBook: Search Inchi
Pubchem (cid): 10722
Pubchem (sid): 134975922
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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
CHEBI: View
CHEMBL: View
Metabolomics Database: Search
UM BBD: Search
KEGG (GenomeNet): C07214
HMDB (The Human Metabolome Database): HMDB29636
FooDB: FDB000806
Export Tariff Code: 2912.29.6000
Typical G.C.
VCF-Online: VCF Volatile Compounds in Food
ChemSpider: View
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Potential Blenders and core components note
 
For Odor
anisic
para-acetanisoleFL/FR
balsamic
 benzyl cinnamateFL/FR
 methyl (E)-cinnamateFL/FR
 methyl cinnamateFL/FR
berry
 raspberry ketone methyl etherFL/FR
camphoreous
 butyrophenoneFL/FR
coumarinic
 phthalideFL/FR
 tonka furanoneFL/FR
creamy
para-vanillic acidFL/FR
ethereal
 cyclohexyl formateFL/FR
floral
para-anisyl nitrileFR
fruity
 allyl 2-ethyl butyrateFL/FR
 allyl benzoateFR
 allyl isovalerateFL/FR
bitter almond oilFL/FR
isoamyl 2-methyl butyrateFL/FR
 amyl butyrateFL/FR
para-anisyl propionateFL/FR
 benzaldehydeFL/FR
 benzaldehyde / methyl anthranilate schiff's baseFR
 benzaldehyde glycrol acetalFL/FR
 bread thiopheneFL/FR
 cherry oxyacetateFL/FR
 cherry pentenoateFL/FR
 cherry propanolFL/FR
 cyclohexyl cinnamateFL/FR
 ethyl benzoyl acetateFL/FR
 ethyl methyl-para-tolyl glycidateFL/FR
 heptyl isobutyrateFL/FR
3-methyl-2-butenalFL/FR
meta-tolualdehydeFL/FR
para-tolualdehydeFL/FR
herbal
laevo-perillaldehydeFL/FR
naphthyl
2,4-dimethyl benzaldehydeFL/FR
nutty
2-acetyl-5-methyl furanFL/FR
 nutty cyclohexenoneFL/FR
phenolic
2'-hydroxyacetophenoneFL/FR
powdery
para-anisyl acetateFL/FR
spicy
 cinnamyl isovalerateFL/FR
para-methoxycinnamaldehydeFL/FR
(E)-para-methoxycinnamaldehydeFL/FR
vanilla
 heliotropyl alcoholFL/FR
 vanillyl acetateFL/FR
 vanillylidene acetoneFL/FR
 
For Flavor
 
No flavor group found for these
para-anisyl propionateFL/FR
 butyrophenoneFL/FR
 ethyl 2-phenyl-3-furoateFL
 heliotropyl alcoholFL/FR
(E)-para-methoxycinnamaldehydeFL/FR
 methyl (E)-cinnamateFL/FR
 methyl furfuracrylateFL
 tonka furanoneFL/FR
anisic
para-acetanisoleFL/FR
aromatic
laevo-perillaldehydeFL/FR
balsamic
 vanillylidene acetoneFL/FR
berry
 heptyl isobutyrateFL/FR
 raspberry ketone methyl etherFL/FR
cherry
para-methoxycinnamaldehydeFL/FR
coumarinic
 phthalideFL/FR
creamy
para-vanillic acidFL/FR
ethereal
 allyl 2-ethyl butyrateFL/FR
 allyl isovalerateFL/FR
bitter almond oilFL/FR
isoamyl 2-methyl butyrateFL/FR
 amyl butyrateFL/FR
para-anisyl acetateFL/FR
 benzaldehydeFL/FR
 benzaldehyde glycrol acetalFL/FR
 bread thiopheneFL/FR
 cherry oxyacetateFL/FR
 cherry pentenoateFL/FR
 cherry propanolFL/FR
 cinnamyl isovalerateFL/FR
 cyclohexyl cinnamateFL/FR
 ethyl benzoyl acetateFL/FR
 ethyl methyl-para-tolyl glycidateFL/FR
3-methyl-2-butenalFL/FR
meta-tolualdehydeFL/FR
green
 cyclohexyl formateFL/FR
naphthyl
2,4-dimethyl benzaldehydeFL/FR
2'-hydroxyacetophenoneFL/FR
nutty
2-acetyl-5-methyl furanFL/FR
 nutty cyclohexenoneFL/FR
powdery
 powdery ketoneFL
spicy
 benzyl cinnamateFL/FR
 methyl cinnamateFL/FR
para-tolualdehydeFL/FR
vanilla
 vanillyl acetateFL/FR
 
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Potential Uses:
None Found
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Occurrence (nature, food, other): note
 allium species - 0.6 mg/kg
Search Trop  Picture
 caraway seed
Search Trop  Picture
 cassia plant
Search Trop  Picture
 coffee
Search  PMC Picture
 garlic bulb
Search Trop  Picture
 tea leaf
Search Trop  Picture
 thevetia peruviana (pers.) k. schum. flower oil brazil @ 1.20%
Data  GC  Search Trop  Picture
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Synonyms:
 benzaldehyde, 2-methyl-
2-formyl toluene
2-formyltoluene
2-methyl benzaldehyde
o-methyl benzaldehyde
ortho-methyl benzaldehyde
2-methyl-benzaldehyde
o-methylbenazldehyde
2-methylbenzaldehyde
o-methylbenzaldehyde
2-tolualdehyde
o-tolualdehyde
o-toluic aldehyde
ortho-toluic aldehyde
ortho-toluyl aldehyde
o-toluylaldehyde
o-tolyl aldehyde
ortho-tolyl aldehyde
o-tolylaldehyde
ortho-tolylaldehyde
Synonyms   Articles   Notes   Search   Top
Articles:
PubMed: [Analysis of volatile components in Qingshanlvshui tea using solid-phase microextraction/accelerated solvent extraction-gas chromatography-mass spectrometry].
PubMed: Evaluation of benzaldehyde derivatives from Morinda officinalis as anti-mite agents with dual function as acaricide and mite indicator.
PubMed: Reaction of selected carbohydrate aldehydes with benzylmagnesium halides: benzyl versus o-tolyl rearrangement.
PubMed: [Study on constituents of essential oil from Lonicera fulvotomentosa in different collected periods].
PubMed: The atmospheric photolysis of o-tolualdehyde.
PubMed: Long-term performance of passive materials for removal of ozone from indoor air.
PubMed: Further investigation into maple syrup yields 3 new lignans, a new phenylpropanoid, and 26 other phytochemicals.
PubMed: 2-Bromo-4-chloro-6-[(E)-o-tolyl-imino-meth-yl]phenol.
PubMed: [Analysis of volatile components in Qingshanlvshui tea using solid-phase microextraction/accelerated solvent extraction-gas chromatography-mass spectrometry].
PubMed: Volatile carbonylic compounds in downtown Santiago, Chile.
PubMed: Inhibitory effects on mushroom tyrosinase by some alkylbenzaldehydes.
PubMed: Biodegradation of dimethylphenols by bacteria with different ring-cleavage pathways of phenolic compounds.
PubMed: Direct observation of aldehyde insertion into rhodium-aryl and -alkoxide complexes.
PubMed: Neurovascular interactions between aldose reductase and angiotensin-converting enzyme inhibition in diabetic rats.
PubMed: Kinetic characteristics of ZENECA ZD5522, a potent inhibitor of human and bovine lens aldose reductase.
PubMed: Oxidation of tolualdehydes to toluic acids catalyzed by cytochrome P450-dependent aldehyde oxygenase in the mouse liver.
PubMed: Embryotoxic effects of acrolein, methacrylates, guanidines and resorcinol on three day chicken embryos.
PubMed: A search for new anticonvulsant compounds among 3-aryl-5-benzylidene derivatives of 2-thiohydantoin.
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