p-Cymene
Synonym(s):p-Cymene;1-Isopropyl-4-methylbenzene;4-Isopropyltoluene;p-Isopropyltoluene
- CAS NO.:99-87-6
- Empirical Formula: C10H14
- Molecular Weight: 134.22
- MDL number: MFCD00008893
- EINECS: 202-796-7
- SAFETY DATA SHEET (SDS)
- Update Date: 2024-08-21 22:41:43
What is p-Cymene?
Description
November is flavor and aroma month!
It’s almost Thanksgiving! Among the holiday treats that most of us enjoy is cranberry sauce, whether it’s full of whole berries or simply a wiggly gelatin. What compounds are in cranberries that make the sauce taste so good?
According to the Science and Food program at the University of California, Los Angeles, the primary flavor compounds are ethyl benzoate, p-cymene, α-terpineol, and 1,8-cineole (aka eucalyptol). The latter two are former Molecules of the Week, so the first two take center stage this year.
Ethyl benzoate is a simple ester of benzoic acid with a sweet, fruity aroma. It has been known since the late 19th century; it is found in fruits such as apples, bananas, cherries, and of course, cranberries. Synthetic ethyl benzoate is made by esterifying benzoic acid and ethanol with an acid catalyst such as hydrochloric or sulfuric acid. It is used as an ingredient in perfumes and artificial fruit-flavoring agents.
p-Cymene is a dialkyl aromatic hydrocarbon. In addition to being a flavor component in cranberries, it is abundant in several essential oils, notably the oils of cumin and thyme. Its aroma and flavor have been described as having hints of citrus, earth, and wood. It can be synthesized from petrochemicals (e.g., the alkylation of toluene with propylene) or from natural terpenes (e.g., by microwave irradiation of limonene). Like ethyl benzoate, p-cymene is used as a flavoring agent; but it also has medicinal uses (in cough syrup) and as a starting material for manufacturing pesticides.
Needless to say, while you’re enjoying your Thanksgiving dinner, you won’t be focusing on any of this. Have a happy holiday!
Chemical properties
p-Cymene is a monoterpene that is found in a variety of plants, including C. sativa, and has diverse biological activities, including antimicrobial, anticancer, antioxidant, anti-inflammatory, antinociceptive, and anxiolytic properties.p-Cymene inhibits the growth of S. typhimurium, E. coli, L. monocytogenes, S. epidermidis, and S. aureus with MIC values ranging from 0.266 to 0.608% v/v.It decreases the invasive activity of HT-1080 human fibrosarcoma cells in vitro by 87% when used at a concentration of 600 μM.In mouse hippocampus, p-Cymene (50 mg/kg, i.p.) reduces lipid peroxidation and nitrite content by 65.5 and 71.2%, respectively, and increases superoxide dismutase (SOD) and catalase activities by 22.7 and 119.3%, respectively, compared to vehicle control animals.Formulations containing p-cymene have been used as flavoring agents.
Occurrence
Widespread in nature; reported in the oils of cypress, Artemisia cina Bg., Ceylon cinnamon, boldo leaf, cascarilla, Cuminum cyminum L. and lemon; in the oils for seeds of coriander and Cicuta virosa; in the ether-extracted oils of Monarda fisulosa and Monarda puncata; in the star anise and nutmeg essential oils. Note that p-cymene reported in essential oil may be formed from the conversion of a cyclic terpene; its presence is indicative of aging in lemon essential oil. Reported found in citrus juices and peel oils, guava, papaya, black currant, pineapple, blueberry, blackberry, carrot, tomato, celery seed, cumin seed, mace, ginger, coriander seed, anise, nutmeg, mace, parsley, cardamom, cinnamon root and bark, pepper, peppermint oil, spearmint oil, cassia leaf and Thymus vulgaris.
The Uses of p-Cymene
As a diluent for lacquers, varnishes, and dyes; in the production of resins; as a component of fragrances; also found as a byproduct in the manufacture of sulfite paper pulp
The Uses of p-Cymene
It is used in heat-exchange media, metal polishes, and thinners for lacquers/varnishes. Also used to make para-cresol, carvacrol, and synthetic resins. It is also used as a component of commercial terpene solvent mixtures.
Definition
ChEBI: A monoterpene that is toluene substituted by an isopropyl group at position 4.
Preparation
Obtained chiefly from the wash water of sulfite paper.
Aroma threshold values
Aroma characteristics at 1% EtoH: harsh chemical, woody and terpy-like with an oxidized citrus lemon note. It has spicy nuances reminiscent of cumin, oregano and cilantro
Taste threshold values
Taste characteristics at 1 to 10 ppm: terpy and rancid with slightly woody, oxidized citrus notes. It has spice nuances of green pepper and oregano.
Synthesis Reference(s)
Journal of the American Chemical Society, 95, p. 982, 1973 DOI: 10.1021/ja00784a090
General Description
Colorless liquid with a mild pleasant odor. Floats on water.
Air & Water Reactions
Insoluble in water.
Reactivity Profile
Vigorous reactions, sometimes amounting to explosions, can result from the contact between aromatic hydrocarbons, such as CYMENE, and strong oxidizing agents. They can react exothermically with bases and with diazo compounds. Substitution at the benzene nucleus occurs by halogenation (acid catalyst), nitration, sulfonation, and the Friedel-Crafts reaction.
Health Hazard
Inhalation causes impairment of coordination, headache. Contact with liquid causes mild irritation of eyes and skin. Ingestion causes irritation of mouth and stomach.
Fire Hazard
HIGHLY FLAMMABLE: Will be easily ignited by heat, sparks or flames. Vapors may form explosive mixtures with air. Vapors may travel to source of ignition and flash back. Most vapors are heavier than air. They will spread along ground and collect in low or confined areas (sewers, basements, tanks). Vapor explosion hazard indoors, outdoors or in sewers. Runoff to sewer may create fire or explosion hazard. Containers may explode when heated. Many liquids are lighter than water.
Flammability and Explosibility
Flammable
Chemical Reactivity
Reactivity with Water: No reaction; Reactivity with Common Materials: No reaction; Stability During Transport: Stable; Neutralizing Agents for Acids and Caustics: Not pertinent; Polymerization: Not pertinent; Inhibitor of Polymerization: Not pertinent.
Safety Profile
Mildly toxic by ingestion. Humans sustain central nervous system effects at low doses. A skin irritant. Flammable liquid. Explosion Hazard: Slight in the form of vapor. To fight fire, use foam, CO2, dry chemical. When heated to decomposition it emits acrid smoke and fumes.
Metabolism
In this compound both an isopropyl and a methyl group occur together and the available evidence shows that only the methyl group is oxidized, cumic acid (pisopropylbenzoic acid) and its conjugate (cuminuric acid) being the main metabolites in dogs and in sheep (Williams, 1959). Following inhalation, only a small part is excreted unchanged, the remainder being oxidized to water-soluble metabolites. As early as 1873, Ziegler suggested that the readily oxidized propyl side-chain formed a -COO H group (Browning, 1965): The ultimate product in the case of dogs and sheep is cumic acid, which is probably excreted as a conjugate with glycine (Gerarde, 1960).
Purification Methods
Wash p-cymene with cold, conc H2SO4 until there is no further colour change, then repeatedly with H2O, 10% aqueous Na2CO3 and H2O again. Dry it over Na2SO4, CaCl2 or MgSO4, and distil it. Further purification steps include steam distillation from 3% NaOH, percolation through silica gel or activated alumina, and a preliminary reflux for several days over powdered sulfur. Store it over CaH2. [Beilstein 5 IV 1060.]
Properties of p-Cymene
Melting point: | -68 °C |
Boiling point: | 176-178 °C(lit.) |
Density | 0.86 g/mL at 25 °C(lit.) |
vapor density | 4.62 (vs air) |
vapor pressure | 1.5 mm Hg ( 20 °C) |
refractive index | n |
FEMA | 2356 | P-CYMENE |
Flash point: | 117 °F |
storage temp. | 2-8°C |
solubility | 23 mg/l |
solubility | Chloroform (Sparingly), Ethyl Acetate (Slightly) |
appearance | colorless liquid |
form | Liquid |
color | Clear |
Odor | Mild, pleasant; aromatic, solvent-type. |
Odor Threshold | 0.057ppm |
explosive limit | 5.6% |
Water Solubility | PRACTICALLY INSOLUBLE |
Merck | 14,2763 |
JECFA Number | 1325 |
BRN | 1903377 |
Dielectric constant | 2.3(17℃) |
Stability: | Stable. Flammable. Incompatible with strong oxidizing agents, strong acids, strong bases. |
CAS DataBase Reference | 99-87-6(CAS DataBase Reference) |
NIST Chemistry Reference | Benzene, 1-methyl-4-(1-methylethyl)-(99-87-6) |
EPA Substance Registry System | p-Cymene (99-87-6) |
Safety information for p-Cymene
Signal word | Danger |
Pictogram(s) |
Flame Flammables GHS02 Health Hazard GHS08 Environment GHS09 |
GHS Hazard Statements |
H226:Flammable liquids H304:Aspiration hazard H411:Hazardous to the aquatic environment, long-term hazard |
Precautionary Statement Codes |
P201:Obtain special instructions before use. P202:Do not handle until all safety precautions have been read and understood. P210:Keep away from heat/sparks/open flames/hot surfaces. — No smoking. P273:Avoid release to the environment. P331:Do NOT induce vomiting. P301+P310:IF SWALLOWED: Immediately call a POISON CENTER or doctor/physician. |
Computed Descriptors for p-Cymene
InChIKey | HFPZCAJZSCWRBC-UHFFFAOYSA-N |
Abamectin manufacturer
Swati Menthol and Allied Chemicals Ltd
New Products
4-Aminotetrahydropyran-4-carbonitrile Hydrochloride (R)-3-Aminobutanenitrile Hydrochloride 4-AMINO-TETRAHYDRO-PYRAN-4-CARBOXYLIC ACID HCL 4-(Dimethylamino)tetrahydro-2H-pyran-4-carbonitrile 3-((Dimethylamino)methyl)-5-methylhexan-2-one oxalate 1,4-Dioxa-8-azaspiro[4.5]decane 5-Bromo-2-nitropyridine Nimesulide BP Aceclofenac IP/BP/EP Diclofenac Sodium IP/BP/EP/USP Mefenamic Acid IP/BP/EP/USP Ornidazole IP Diclofenac Potassium SODIUM AAS SOLUTION ZINC AAS SOLUTION BUFFER SOLUTION PH 10.0(BORATE) GOOCH CRUCIBLE SINTERED AQUANIL 5 BERYLLIUM AAS SOLUTION 2-Bromo-1-(bromomethyl)-3-chloro-5-nitrobenzene 2-Bromo-3-nitroaniline N-(3-Hydroxypropyl)-N-methylacetamide 3-Bromo-6-chloropyridazine 4-ethyl-3-nitrobenzoic acidRelated products of tetrahydrofuran
You may like
-
99-87-6 98%View Details
99-87-6 -
p-Cymene 98%View Details
99-87-6 -
p-Cymene CAS 99-87-6View Details
99-87-6 -
p-Cymene CAS 99-87-6View Details
99-87-6 -
p-Cymene solution CAS 99-87-6View Details
99-87-6 -
p-Cymene CAS 99-87-6View Details
99-87-6 -
p-Cymene CAS 99-87-6View Details
99-87-6 -
p-Cymene CAS 99-87-6View Details
99-87-6