Description Chemical Properties Uses Production Methods References
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p-Cymene

Description Chemical Properties Uses Production Methods References
Product Name
p-Cymene
CAS No.
99-87-6
Chemical Name
p-Cymene
Synonyms
Cymene;Cymol;4-ISOPROPYLTOLUENE;PARA CYMENE;P-ISOPROPYLTOLUENE;1-METHYL-4-ISOPROPYLBENZENE;P-CYMOL;lsopropyltoluene;1-Methyl-4-(1-methylethyl)-benzene;4-CYMENE
CBNumber
CB9262508
Molecular Formula
C10H14
Formula Weight
134.22
MOL File
99-87-6.mol
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p-Cymene Property

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 
n20/D 1.490(lit.)
FEMA 
2356 | P-CYMENE
Flash point:
117 °F
storage temp. 
2-8°C
solubility 
Chloroform (Sparingly), Ethyl Acetate (Slightly)
form 
Liquid
color 
Clear
Odor
Mild, pleasant; aromatic, solvent-type.
Odor Type
terpenic
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.
InChIKey
HFPZCAJZSCWRBC-UHFFFAOYSA-N
LogP
4.1-4.8 at 20℃
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)
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Safety

Hazard Codes 
Xi
Risk Statements 
10-36/37/38
Safety Statements 
26-36
RIDADR 
UN 2046 3/PG 3
WGK Germany 
2
RTECS 
GZ5950000
Autoignition Temperature
817 °F
TSCA 
Yes
HazardClass 
3
PackingGroup 
III
HS Code 
29029090
Hazardous Substances Data
99-87-6(Hazardous Substances Data)
Toxicity
LD50 orally in rats: 4750 mg/kg (Jenner)
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Hazard statements

H226Flammable liquid and vapour

H304May be fatal if swallowed and enters airways

H411Toxic to aquatic life with long lasting effects

Precautionary statements

P201Obtain special instructions before use.

P202Do not handle until all safety precautions have been read and understood.

P210Keep away from heat/sparks/open flames/hot surfaces. — No smoking.

P273Avoid release to the environment.

P301+P310IF SWALLOWED: Immediately call a POISON CENTER or doctor/physician.

P331Do NOT induce vomiting.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
W235601
Product name
p-Cymene
Purity
≥97%, FG
Packaging
1kg
Price
$73.2
Updated
2024/03/01
Sigma-Aldrich
Product number
W235601
Product name
p-Cymene
Purity
≥97%, FG
Packaging
8kg
Price
$282
Updated
2024/03/01
Sigma-Aldrich
Product number
W235601
Product name
p-Cymene
Purity
≥97%, FG
Packaging
20kg
Price
$494
Updated
2024/03/01
Sigma-Aldrich
Product number
PHL80836
Product name
p-Cymene
Purity
phyproof? Reference Substance
Packaging
100MG
Price
$262
Updated
2024/03/01
Sigma-Aldrich
Product number
CRM40419
Product name
p-Cymene solution
Purity
certified reference material, 2000?μg/mL in methanol, ampule of 1?mL
Packaging
1mL
Price
$129
Updated
2024/03/01
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p-Cymene Chemical Properties,Usage,Production

Description

p-Cymene is a naturally occurring compound, although it has two further geometric isomers, m-cymene (with meta-substituted alkyl groups) and o-cymene (with ortho-substituted alkyl groups) which do not occur naturally. p-Cymene is related to the monoterpenes. Monoterpenes themselves belong to the “terpenes”, a larger class of organic compounds, which are the most representative components of essential oils. chemical structure of p-cymene, indicating the benzene ring with methyl and isopropyl substitutions.

chemical structure of p-cymene

Chemical Properties

p-Cymene has a citrusy aroma reminiscent of lemon. It is colorless liquid with a strong, characteristic odor reminiscent of carrot. It tends to darken with aging. It occurs naturally in orange peel oil, mandarin peel oil, satsuma mandarin peel oil, coldpressed lime peel oil, distilled lime peel oil, cinnamon leaf, etc. 4-isopropyltoluene has antimicrobial properties. It is used as a flavor ingredient permitted for direct addition to food for human consumption.

Uses

p-Cymene is an alkyl aromatic hydrocarbon mainly used to study oxidation reactions under various conditions to synthesize highly valuable intermediates and building-blocks such as cymene hydroperoxide, 4-methyl acetophenone, 4-isopropyl benzyl alcohol, 4-isopropyl benzaldehyde and 4-isopropyl benzoic acid etc.
Medicinally, p-cymene is used to prevent coughs and eliminate phlegm as well as being a flavouring agent, and being used in the production of fungicides and pesticides. It is considered to be “generally recognised as safe” (GRAS) by the U.S. Food and Drug Administration. Its potential in the prevention of protein glycation mediated diabetic complications has also been confirmed, and it has been suggested as an in vivo antioxidant compound due to its ability to reduce the formation of oxygen and nitrogen reactive species, acting as a potential neuroprotective agent in the brain. Therefore, it could be involved in the treatment of oxidative stress related diseases.

Production Methods

p-cymene is conventionally produced by the Friedel-Crafts alkylation of toluene with isopropanol, or of benzene with methyl or isopropyl halides.

References

[1] George A. Burdock, Encyclopedia of Food and Color Additives, Volume 1, 1996
[2] C.F. Bagamboula, M. Uyttendaele and J. Debevere, Inhibitory effect of thyme and basil essential oils, carvacrol, thymol, estragol, linalool and p-cymene towards Shigella sonnei and S. flexneri, Food Microbiology, 2004, vol. 21, 33-42

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.

Uses

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

Uses

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.

Preparation

Obtained chiefly from the wash water of sulfite paper.

Definition

ChEBI: A monoterpene that is toluene substituted by an isopropyl group at position 4.

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.]

p-Cymene Preparation Products And Raw materials

Raw materials

Preparation Products

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p-Cymene Suppliers

Jiangxi Linyuan Spicse Co., Ltd.
Tel
182-96617057 19318896872
Fax
0796-8287629
Email
893227524@qq.com
Country
China
ProdList
377
Advantage
58
Jiangxi Baolin Natural Spices Co.Ltd.
Tel
0796-8180428 13576833965
Fax
0796-8116585
Email
1510355607@qq.com
Country
China
ProdList
118
Advantage
58
QINGDAO CHENXI NEW ENERGYCO.LTD
Tel
19012836015
Email
cxxny88882022@163.com
Country
China
ProdList
59
Advantage
58
Meryer (Shanghai) Chemical Technology Co., Ltd.
Tel
021-61259108 18621169109
Fax
86-21-61259102
Email
market03@meryer.com
Country
China
ProdList
40228
Advantage
62
Alfa Aesar
Tel
400-6106006
Fax
021-67582001/03/05
Email
saleschina@alfa-asia.com
Country
China
ProdList
30123
Advantage
84
TAIYUAN RHF CO.,LTD.
Tel
+86 351 7031519
Fax
+86 351 7031519
Email
sales@RHFChem.com
Country
China
ProdList
2338
Advantage
56
TCI (Shanghai) Development Co., Ltd.
Tel
021-67121386
Fax
021-67121385
Email
Sales-CN@TCIchemicals.com
Country
China
ProdList
24529
Advantage
81
Energy Chemical
Tel
021-021-58432009 400-005-6266
Fax
021-58436166
Email
sales8178@energy-chemical.com
Country
China
ProdList
44689
Advantage
61
Pure Chemistry Scientific Inc.
Tel
001-857-928-2050 or 1-888-588-9418
Fax
001-617-206-9595
Email
sales@chemreagents.com
Country
United States
ProdList
10186
Advantage
62
Shanghai Hanhong Scientific Co.,Ltd.
Tel
021-54306202 13764082696
Email
info@hanhongsci.com
Country
China
ProdList
42958
Advantage
64
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View Lastest Price from p-Cymene manufacturers

Hebei Chuanghai Biotechnology Co,.LTD
Product
p-cymene 99-87-6
Price
US $4.60/KG
Min. Order
1KG
Purity
98%
Supply Ability
5000kg
Release date
2024-08-20
Hebei Weibang Biotechnology Co., Ltd
Product
p-Cymene 99-87-6
Price
US $10.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
100 mt
Release date
2021-11-03
Hebei Mojin Biotechnology Co., Ltd
Product
p-Cymene 99-87-6
Price
US $0.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
50000KG/month
Release date
2023-08-17

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