γ-Terpinene
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γ-Terpinene
structure -
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CAS No:
99-85-4
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Formula:
C10H16
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Chemical Name:
γ-Terpinene
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Synonyms:
1,4-Cyclohexadiene,1-methyl-4-(1-methylethyl)-;p-Mentha-1,4-diene;1-Methyl-4-(1-methylethyl)-1,4-cyclohexadiene;Crithmene;gamma-Terpinene;Moslene;γ-Terpinene;γ-Terpinen;4-Isopropyl-1-methyl-1,4-cyclohexadiene;1-Methyl-4-isopropyl-1,4-cyclohexadiene;1-Isopropyl-4-methyl-1,4-cyclohexadiene;NSC 21448;1-Methyl-4-(propan-2-yl)cyclohexa-1,4-diene;1-Methyl-4-propan-2-ylcyclohexa-1,4-diene
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CAS No:
Description
clear liquid γ-Terpinene is a colorless liquid with an herbaceous citrus odor and can be prepared by isomerization of limonene. p-Mentha-1,4-diene has a characteristic lemon odor (not as lemony as the alpha-isomer, but warmer). It has a slightly bitter, herbaceous, citrus-like flavor; woody, terpene, tropical lemon odor.
Liquid|Colourless oily liquid; refreshing, herbaceous-citrusy aroma
Gamma-terpinene is one of three isomeric monoterpenes differing in the positions of their two double bonds (alpha- and beta-terpinene being the others). In gamma-terpinene the double bonds are at the 1- and 4-positions of the p-menthane skeleton. It has a role as an antioxidant, a plant metabolite, a volatile oil component and a human xenobiotic metabolite. It is a monoterpene and a cyclohexadiene.
Characteristics
0
2.8
White Powder or Cyrstals
0.849 g/cm3 @ Temp: 20 °C
-10 °C
183 °C
125 °F
1.474
water: soluble 5%, clear, colorless to faintly yellow
2-8°C
~0.7 mm Hg ( 20 °C)
4.7 (vs air)
1.77e-10 cm3/molecule*sec
0.03 atm-m3/mole
Safety Information
III
3.2
UN 2319 3/PG 3
2
10-36/37/38
26-36
OS8070000
Xi
P210, P233, P240, P241, P242, P243, P280, P301+P310, P303+P361+P353, P331, P370+P378, P403+P235, P405, P501
H226
|Danger|H226 (99.54%): Flammable liquid and vapor [Warning Flammable liquids]|P210, P233, P240, P241, P242, P243, P280, P301+P310, P303+P361+P353, P331, P370+P378, P403+P235, P405, and P501|Aggregated GHS information provided by 1966 companies from 24 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
γ-Terpinene Use and Manufacturing
Derived from Lantana camara essential oil. From p-cymene in liquid ammonia with ethanol and sodium reaction (Birch reaction) derived.
spices. Mainly used to formulate essential oils of artificial lemon and mint.
Odor agents
Air care products
100,000 - 500,000 lb
Soap, cleaning compound, and toilet preparation manufacturing|1,4-Cyclohexadiene, 1-methyl-4-(1-methylethyl)-: ACTIVE
EPA Safer Chemical Functional Use Classes -> Fragrances|Safer Chemical Classes -> Yellow triangle - The chemical has met Safer Choice Criteria for its functional ingredient-class, but has some hazard profile issues|Food additives -> Flavoring Agents|Flavoring Agents -> JECFA Flavorings Index|Lipids -> Prenol Lipids [PR] -> Isoprenoids [PR01] -> C10 isoprenoids (monoterpenes) [PR0102]
Flavoring Agents
Computed Properties
Molecular Weight:136.23
XLogP3:2.8
Rotatable Bond Count:1
Exact Mass:136.125200510
Monoisotopic Mass:136.125200510
Heavy Atom Count:10
Complexity:171
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
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