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p-Cymene

p-Cymene Structure
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
Molecular Weight:
134.22
MOL File:
99-87-6.mol
MSDS File:
SDS
Modify Date:
2024/8/21 22:41:43

p-Cymene Properties

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)
FEMA 2356 | P-CYMENE
refractive index n20/D 1.490(lit.)
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 Threshold 0.057ppm
explosive limit 5.6%
Odor Type terpenic
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)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS02,GHS08,GHS09
Signal word  Danger
Hazard statements  H226-H304-H361f-H411
Precautionary statements  P201-P202-P210-P273-P301+P310-P331
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
Toxicity LD50 orally in rats: 4750 mg/kg (Jenner)
NFPA 704
2
1 0

p-Cymene price More Price(13)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) W235601 p-Cymene ≥97%, FG 99-87-6 1SAMPLE-K ₹4880.63 2022-06-14 Buy
Sigma-Aldrich(India) W235601 p-Cymene ≥97%, FG 99-87-6 1KG ₹7315.8 2022-06-14 Buy
Sigma-Aldrich(India) W235601 p-Cymene ≥97%, FG 99-87-6 20KG ₹46247.78 2022-06-14 Buy
Sigma-Aldrich(India) C121452 p-Cymene 99% 99-87-6 25ML ₹2620.13 2022-06-14 Buy
Sigma-Aldrich(India) C121452 p-Cymene 99% 99-87-6 1L ₹3760.65 2022-06-14 Buy
Product number Packaging Price Buy
W235601 1SAMPLE-K ₹4880.63 Buy
W235601 1KG ₹7315.8 Buy
W235601 20KG ₹46247.78 Buy
C121452 25ML ₹2620.13 Buy
C121452 1L ₹3760.65 Buy

p-Cymene Chemical Properties,Uses,Production

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

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.

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.

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.]

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1-(1-methylethyl)-4-methylbenzene 1-isopropyl-4-methyl-benzen 1-methyl-4-(1-methylethyl)-benzen 1-methyl-4-(1-methylethyl)benzene 1-methyl-4-(1-methyl-ethyl)-benzene 1-methyl-4-1-methylethylbenzene p-Isopropyltoluol p-Mentha-1,3,5-triene p-methyl-cumen p-Methylisopropylbenzene 4-lsopropyltoluene PARA CYMENE P&F FCC P-ISOPROPYLTOLUENE, 1000MG, NEAT P-CYMENE 97+% FCC P-CYMENE, STANDARD FOR GC P-CYMENE, FREE OF TERPENES 4-Isopropyltoluene 4-Methylisopropylbenzene p-Cymene p-CyMene 99% p-CyMene, >=99.5% (GC) p-Cymene Dolcymene p-Isopropyltoluene 1-Isopropyl-4-methylbenzene DOLCYMENE CYMENE, 4- Methyl isopropyl benzene 4-(2-propyl)toluene 4-Isopropyl-1-methylbenzene Benzene, 1-isopropyl-4-methyl- benzene, 1-methyl-4-methylethyl- benzene,1-(1-methylethyl)-4-methyl- Benzene,1-methyl-4-(1-methylethyl)- Camphogen Cumene, p-methyl- iso-Propyl-p-toluene isopropyltoluol methylpropylbenzene Paracymol p-Isopropylmethylbenzene METHYL(1-METHYLETHYL)BENZENE P-METHYLPROPYLBENZENE P-CYMENE PARA-CYMENE 97 p-Cymene, 99+% p-cymene,4-isopropyltoluene;p-methylcumene 1-methyl-4-propan-2-yl-benzene CYMENE, 4-(SG) 4-Isopropyltoluene (p-Cymene) (95-98%) PARA-METHYL-ISOPROPYL-BENZENE 4-ISOPROPYL-METHYLBENZENE PARA-ISOPROPYLTOLUENE CYMOL-PARA REIN Benzene,1-methyl-4-(1-meth 4-lsopropyltoluene Standard 4-ISOPROPYLTOLUENE / P-CYMENE 4-Isopropyltoluene (=p-Cymene) (1mg/ml in Methanol) [for Water Analysis] Cymen (meylisopropylbenzine) 1-Isopropyl-4-methylbenzene, 4-Isopropyltoluene 1-Isopropyl-4-methylbenzene, 4-Isopropyltoluene, p-Cymene 4-CYMENE WITH GC