We have found 46587 results matching your criteria.
Please wait while we search...

General Material Information

Preferred name meta-cresol
Trivial Name m-Cresol
Short Description m-cresol
Formula C7 H8 O
CAS Number 108-39-4
FEMA Number 3530
Flavis Number 4.026
ECHA Number 203-577-9
FDA UNII GGO4Y809LO
Nikkaji Number J1.186J
Beilstein Number 0506719
MDL MFCD00002302
COE Number 617
Bio Activity Summary External link
NMR Predictor External link
JECFA Food Flavoring 692 m-cresol
FDA Patent No longer provide for the use of these seven synthetic flavoring substances
FDA Mainterm 108-39-4 ; M-CRESOL
Synonyms
  • 3-cresol
  • m- cresol
  • m- cresol food grade
  • cresol meta pure
  • meta- cresol N- grade
  • m- cresylic acid
  • meta- cresylic acid
  • 1-hydroxy-3-methyl benzene
  • 1-hydroxy-3-methylbenzene
  • 3-hydroxytoluene
  • 3-methyl phenol
  • meta- methyl phenol
  • 3-methyl-1-hydroxybenzene
  • 1-methyl-3-hydroxybenzene
  • 3-methylphenol
  • m- methylphenol
  • 3-methylphenol
  • Phenol, 3-methyl-
  • m-Cresol
  • m-Cresylic acid
  • m-Kresol
  • m-Oxytoluene
  • 1-Hydroxy-3-methylbenzene
  • 3-Cresol
  • 3-Hydroxytoluene
  • m-Toluol
  • m-Methylphenol
  • m-Hydroxytoluene
  • NSC 8768

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

Google Scholar Start search
Google Books Start search
Google Patents Start search
Perfumer & Flavorists Start search
EU Patents Start search
PubMeb Start search
NCBI Start search

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
FDA Indirect Additives used in Food Contact Substances:View
CHEBI:View
CHEMBL:View
Metabolomics Database:Search
UM BBD:Search
KEGG (GenomeNet):C01467
HMDB (The Human Metabolome Database):HMDB02048
FooDB:FDB008788
YMDB (Yeast Metabolome Database):YMDB01730
Export Tariff Code:2907.12.0000
Typical G.C.
VCF-Online:VCF Volatile Compounds in Food
Wikipedia:View
Wikipedia2:View2
Formulations/Preparations:
•grade: technical (95-98%) •pure cresol is a mixture of ortho-, meta- & para-isomers. crude cresol (commercial cresol) is a mixture of aromatic cmpd containing about 20% of o-cresol, 40% of m-cresol, & 30% of p-cresol with small amt of phenol & xylenols. •franklin cresolis, 50% m-cresol, 31% soap cancelled •saponated cresol solution n.f., 50% m-cresol, 35% soap cancelled •bacticin, 0.4660% m-cresol, 0.4630% 2,4-xylenol cancelled •celcure dry mix (chemicals for wood preserving), 5% m-cresol, 50% copper sulfate pentahydrate, 45% potassium dichromate cancelled •rover's dog shampoo, 0.4% m-cresol, 1.0% paradichlorobenzene, 0.1% pine oil, 19.3% soap cancelled •gallex, 0.4660% m-cresol, 0.4630% 2,4-xylenol active •generally m- and p- isomers are used industrially as a mixture containing 40% to 65% m-cresol.

PhysChem Properties

Material listed in food chemical codex No
Molecular weight 108.13996124268
Specific gravity @ 20 °C
Pounds per Gallon 8.614 to 8.639
Refractive Index 1.538 to 1.542 @ 20 °C
Melting Point 11 to 12°C @ 760 mm Hg
Boiling Point 202 to 203°C @ 760 mm Hg
Boiling Point 120 to 121°C @ 50 mm Hg
Vapor Pressure 0.11 mmHg @ 25 °C
Vapor Density 7.07
Flash Point TCC Value 86.11 °C TCC
logP (o/w) 1.96
Solubility
alcohol Yes
water, 8890 mg/L @ 25 °C (est) Yes
water, 2.27E+04 mg/L @ 25 °C (exp) Yes
water No

Organoleptic Properties

Odor Type: Phenolic
medicinal, woody, leathery, phenolic
Odor strength high , recommend smelling in a 0.01 % solution or less
Substantivity 43 hour(s) at 100.00 %
Luebke, William tgsc, (1995) At 0.01 % in dipropylene glycol. medicinal woody leather phenolic
General comment Medicinal; woody; ethereal
Arctander has this to say about it: “Dry-tarry, medicinal-leathery odor, conventionally described as “phenolic. Useful as a floralizing companion to Indole in sharp-exotic flower fragrances, Lily (Bermuda-lily, etc.), Narcisse, etc. Concentration in the perfume composition will usually be about 0.1%, sometimes slightly higher, mostly lower than 0.1%.” Medicinal, woody, leather, phenolic

Occurrences

Potential Uses

Applications
Odor purposes Castoreum, Myrrh
Other purposes Antimicrobial agents
Cosmetic purposes Antimicrobial agents, Perfuming agents

Safety Information

Safety information

Preferred SDS: View
European information :
Most important hazard(s):
T - Toxic.
R 24/25 - Toxic in contact with skin and if swallowed.
R 34 - Causes burns.
S 02 - Keep out of the reach of children.
S 36/37/39 - Wear suitable clothing, gloves and eye/face protection.
S 45 - In case of accident or if you feel unwell seek medical advice immediately.
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:
oral-rat LD50 [sex: M] 242 mg/kg
(E.I. du Pont de Nemours & Company, 1969a)

oral-mouse LD50 828 mg/kg
(E.I. du Pont de Nemours & Company, 1969a)

intraperitoneal-mouse LD50 168 mg/kg
(E.I. du Pont de Nemours & Company, 1969a)

gavage-rat LD50 [sex: M] 520 mg/kg
(Carpenter, 1949b)

oral-rat LD50 242 mg/kg
GASTROINTESTINAL: PERITONITIS BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY)
BIOFAX Industrial Bio-Test Laboratories, Inc., Data Sheets. Vol. 3-5/1969

oral-rabbit LDLo 1400 mg/kg
Journal of Pharmacology and Experimental Therapeutics. Vol. 80, Pg. 233, 1944.

intravenous-rabbit LDLo 280 mg/kg
Journal of Pharmacology and Experimental Therapeutics. Vol. 80, Pg. 233, 1944.

oral-mouse LD50 828 mg/kg
Gigiena Truda i Professional'nye Zabolevaniya. Labor Hygiene and Occupational Diseases. Vol. 18(2), Pg. 58, 1974.

intraperitoneal-mouse LD50 168 mg/kg
"Handbook of Toxicology," 4 vols., Philadelphia, W.B. Saunders Co., 1956-59Vol. 5, Pg. 56, 1959.

intraperitoneal-guinea pig LDLo 100 mg/kg
"Abdernalden's Handbuch der Biologischen Arbeitsmethoden." Vol. 4, Pg. 1361, 1935.

Dermal Toxicity:
subcutaneous-rat LDLo 900 mg/kg
"Handbook of Toxicology," 4 vols., Philadelphia, W.B. Saunders Co., 1956-59Vol. 5, Pg. 56, 1959.

skin-rat LD50 1100 mg/kg
Gigiena Truda i Professional'nye Zabolevaniya. Labor Hygiene and Occupational Diseases. Vol. 18(2), Pg. 58, 1974.

subcutaneous-rabbit LDLo 500 mg/kg
"Abdernalden's Handbuch der Biologischen Arbeitsmethoden." Vol. 4, Pg. 1361, 1935.

subcutaneous-mouse LDLo 450 mg/kg
"Abdernalden's Handbuch der Biologischen Arbeitsmethoden." Vol. 4, Pg. 1361, 1935.

subcutaneous-guinea pig LDLo 300 mg/kg
"Handbook of Toxicology," 4 vols., Philadelphia, W.B. Saunders Co., 1956-59Vol. 5, Pg. 56, 1959.

subcutaneous-cat LDLo 180 mg/kg
Journal of Pharmacology and Experimental Therapeutics. Vol. 80, Pg. 233, 1944.

Inhalation Toxicity:
inhalation-rat LC50 > 710 mg/m3/1H
Journal of Pharmacology and Experimental Therapeutics. Vol. 80, Pg. 233, 1944.

Safety in use information

Category:
food contact resinous and polymeric coatings
RIFM Fragrance Material Safety Assessment: Search
IFRA Code of Practice Notification of the 49th Amendment to the IFRA Code of Practice
Recommendation for meta-cresol usage levels up to:
0.0100 % in the fragrance concentrate.
Maximised Survey-derived Daily Intakes (MSDI-EU): 0.12 (μg/capita/day)
Maximised Survey-derived Daily Intakes (MSDI-USA): 0.10 (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: 11. Update in publication number(s): 29
Click here to view publication 11
average usual ppmaverage maximum ppm
baked goods: 0.500001.00000
beverages(nonalcoholic): --
beverages(alcoholic): 0.300001.00000
breakfast cereal: 0.500005.00000
cheese: 0.100000.50000
chewing gum: 0.100000.50000
condiments / relishes: 0.100000.50000
confectionery froastings: 0.100000.50000
egg products: 0.100000.50000
fats / oils: 0.100000.50000
fish products: 0.500005.00000
frozen dairy: 0.100000.50000
fruit ices: 0.100000.50000
gelatins / puddings: 0.100000.50000
granulated sugar: 0.100000.50000
gravies: 0.300000.50000
hard candy: 0.100000.50000
imitation dairy: 0.100000.50000
instant coffee / tea: 0.300000.50000
jams / jellies: 0.100000.50000
meat products: 0.300001.00000
milk products: 0.100000.50000
nut products: 0.300000.50000
other grains: 0.500005.00000
poultry: 0.500005.00000
processed fruits: --
processed vegetables: --
reconstituted vegetables: --
seasonings / flavors: 1.0000010.00000
snack foods: 0.300000.50000
soft candy: --
soups: 0.300000.50000
sugar substitutes: 0.100000.50000
sweet sauces: 0.100000.50000

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

Flavouring Group Evaluation 60 (FGE.60): Consideration of eugenol and related hydroxyallylbenzene derivatives evaluated by JECFA (65th meeting) structurally related to ring- substituted phenolic substances evaluated by EFSA in FGE.22 (2006)
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

Scientific Opinion on the safety and efficacy of phenol derivatives containing ring-alkyl, ring-alkoxy and side-chains with an oxygenated functional group (chemical group 25) when used as flavourings for all species
View page or View pdf

EPI System: View
EPA-Iris:IRIS
NIOSH International Chemical Safety Cards:search
NIOSH Pocket Guide:search
Chemical Carcinogenesis Research Information System:Search
AIDS Citations:Search
Cancer Citations:Search
Toxicology Citations:Search
EPA GENetic TOXicology:Search
EPA Substance Registry Services (TSCA):108-39-4
EPA ACToR:Toxicology Data
EPA Substance Registry Services (SRS):Registry
Laboratory Chemical Safety Summary :342
National Institute of Allergy and Infectious Diseases:Data
WISER:UN 2076
WGK Germany:1
3-methylphenol
Chemidplus:0000108394
EPA/NOAA CAMEO:hazardous materials
RTECS:108-39-4