ChemicalBook
Chinese Japanese Germany Korea

p-Cymene

Description Chemical Properties Uses Production Methods References
p-Cymene
p-Cymene structure
CAS No.
99-87-6
Chemical Name:
p-Cymene
Synonyms
Cymol;Cymene;P-CYMOL;4-CYMENE;NSC 4162;p-Cimene;P-CYMENE;P - ISO -;DOLCYMENE;FEMA 2356
CBNumber:
CB9262508
Molecular Formula:
C10H14
Formula Weight:
134.22
MOL File:
99-87-6.mol

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)
refractive index 
n20/D 1.490(lit.)
FEMA 
2356 | P-CYMENE
Flash point:
117 °F
storage temp. 
2-8°C
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
Stability:
Stable. Flammable. Incompatible with strong oxidizing agents, strong acids, strong bases.
InChIKey
HFPZCAJZSCWRBC-UHFFFAOYSA-N
CAS DataBase Reference
99-87-6(CAS DataBase Reference)
Substances Added to Food (formerly EAFUS)
P-CYMENE
FDA 21 CFR
172.515
FDA UNII
1G1C8T1N7Q
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,GHS07
Signal word  Danger
Hazard statements  H315-H319-H336-H226-H304-H411-H302-H335
Precautionary statements  P233-P240-P241+P242+P243-P261-P264-P271-P273-P280-P301+P310+P331-P302+P352+P332+P313+P362+P364-P304+P340+P312-P305+P351+P338+P337+P313-P391-P403+P233-P405-P501-P303+P361+P353-P305+P351+P338-P501a-P210-P301+P310-P331-P370+P378
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(20)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich W235601 p-Cymene ≥97%, FG 99-87-6 1 kg $67 2021-03-22 Buy
Sigma-Aldrich 30039 p-Cymene analytical standard 99-87-6 5ml $74.3 2021-03-22 Buy
Sigma-Aldrich CRM40419 p-Cymene solution certified reference material, 2000?μg/mL in methanol, ampule of 1?mL 99-87-6 1 mL $100 2021-03-22 Buy
Sigma-Aldrich 49679 p-Cymene certified reference material, TraceCERT 99-87-6 100mg $201 2020-08-18 Buy
Sigma-Aldrich W235601 p-Cymene ≥97%, FG 99-87-6 8 kg $217 2021-03-22 Buy

p-Cymene Chemical Properties,Uses,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 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

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.

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


p-Cymene Suppliers

Global( 238)Suppliers
Supplier Tel Fax Email Country ProdList Advantage
career henan chemical co
+86-371-86658258
sales@coreychem.com CHINA 29955 58
NINGBO INNO PHARMCHEM CO., LTD.
13867897135
sales@nbinno.com CHINA 925 58
Hubei Jusheng Technology Co.,Ltd.
86-18871470254
027-59599243 linda@hubeijusheng.com CHINA 28229 58
Hebei Guanlang Biotechnology Co., Ltd.
+8619930503282
sales3@crovellbio.com China 5912 58
Chongqing Chemdad Co.,Ltd
+86-19923101450
sales@chemdad.com CHINA 4000 58
Xiamen AmoyChem Co., Ltd
+86 592-605 1114
sales@amoychem.com CHINA 6369 58
Hubei xin bonus chemical co. LTD
86-13657291602
027-59338440 linda@hubeijusheng.com CHINA 23035 58
Shandong chuangyingchemical Co., Ltd.
18853181302
sale@chuangyingchem.com CHINA 5917 58
Standardpharm Co. Ltd.
86-714-3992388
overseasales1@yongstandards.com United States 14344 58
Chongqing Chemdad Co., Ltd
+86-13650506873
sales@chemdad.com CHINA 37282 58

View Lastest Price from p-Cymene manufacturers

Image Release date Product Price Min. Order Purity Supply Ability Manufacturer
2021-12-01 p-cymene
99-87-6
US $4.60 / KG 1KG 98% 5000kg Hebei Crovell Biotech Co Ltd
2021-11-04 p-Cymene
99-87-6
US $10.00 / KG 1KG 99% 100 mt Hebei Guanlang Biotechnology Co., Ltd.
2021-07-02 p-Cymene
99-87-6
US $15.00-10.00 / KG 1KG 99%+ HPLC Monthly supply of 1 ton Zhuozhou Wenxi import and Export Co., Ltd

p-Cymene Spectrum


99-87-6(p-Cymene)Related Search:


Copyright 2017 © ChemicalBook. All rights reserved