This is a demo store. No orders will be fulfilled.

 
Call +1 (833) 552-7181 or Contact us
Toggle Nav
My Cart
Search
Advanced Search
Menu
Account
Settings
྾
main product photo

γ-Terpinene - >95.0%(GC), high purity , CAS No.99-85-4

16 Citations COA COA
    Grade & Purity:
  • ≥95%(GC)
In stock
Item Number
G156812
Grouped product items
SKU Size
Availability
 Price Qty
G156812-5ml
5ml
2
$9.90
G156812-25ml
25ml
2
$22.90
G156812-100ml
100ml
3
$82.90
G156812-500ml
500ml
2
$125.90
Wish List
Bulk Order  SDS  DATASHEET  Specification Sheet
View related series
Bacterial (3013) Fungal (844) Non heterocyclic block (8163) terpenes (123)

Basic Description

Synonyms .gamma.-Terpinen | EINECS 202-794-6 | BS-23574 | gamma-Terpinene, analytical standard | HY-W020183 | 1-methyl-4-propan-2-ylcyclohexa-1,4-diene | InChI=1/C10H16/c1-8(2)10-6-4-9(3)5-7-10/h4,7-8H,5-6H2,1-3H | 1-Methyl-4-isopropyl-1,4-cyclohexadiene | gamma-T
Specifications & Purity ≥95%(GC)
Storage Temp Store at 2-8°C,Argon charged
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Product Description

γ-Terpinene is a monoterpene hydrocarbon present in essential oils extracted from Thymus vulgaris L., and exhibits antimicrobial, carminative and expectorant activities.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Hydrocarbons
Class Unsaturated hydrocarbons
Subclass Branched unsaturated hydrocarbons
Intermediate Tree Nodes Not available
Direct Parent Branched unsaturated hydrocarbons
Alternative Parents Cyclic olefins  Unsaturated aliphatic hydrocarbons  
Molecular Framework Aliphatic homomonocyclic compounds
Substituents Branched unsaturated hydrocarbon - Cyclic olefin - Unsaturated aliphatic hydrocarbon - Olefin - Aliphatic homomonocyclic compound
Description This compound belongs to the class of organic compounds known as branched unsaturated hydrocarbons. These are hydrocarbons that contains one or more unsaturated carbon atoms, and an aliphatic branch.
External Descriptors a monoterpenoid

Associated Targets(Human)

ACHE Tclin Acetylcholinesterase (18204 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Associated Targets(non-human)

Pseudomonas aeruginosa (123386 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Staphylococcus aureus (210822 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Klebsiella aerogenes (4963 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Escherichia coli (133304 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Streptococcus mutans (2687 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Aspergillus flavus (8875 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Bacillus subtilis (32866 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Cyberlindnera jadinii (900 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Saccharomyces cerevisiae (19171 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Corynebacterium ammoniagenes (75 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Cutibacterium acnes (887 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Penicillium chrysogenum (1593 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Leptinotarsa decemlineata (1161 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Malassezia furfur (70 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Mechanisms of Action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References

Names and Identifiers

Pubchem Sid 504751351
Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/504751351
IUPAC Name 1-methyl-4-propan-2-ylcyclohexa-1,4-diene
INCHI InChI=1S/C10H16/c1-8(2)10-6-4-9(3)5-7-10/h4,7-8H,5-6H2,1-3H3
InChIKey YKFLAYDHMOASIY-UHFFFAOYSA-N
Smiles CC1=CCC(=CC1)C(C)C
Isomeric SMILES CC1=CCC(=CC1)C(C)C
WGK Germany 2
RTECS OS8070000
Molecular Weight 136.24
Beilstein 5128
Reaxy-Rn 2038347
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2038347&ln=

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

13 results found

Lot Number Certificate Type Date Item
A2108081 Certificate of Analysis Nov 18, 2024 G156812
B2327157 Certificate of Analysis Jun 23, 2022 G156812
F23061490 Certificate of Analysis Jun 23, 2022 G156812
I2202559 Certificate of Analysis Jun 23, 2022 G156812
D2415408 Certificate of Analysis Jun 23, 2022 G156812
I2202560 Certificate of Analysis Jun 23, 2022 G156812
F2526086 Certificate of Analysis Jun 23, 2022 G156812
G2501068 Certificate of Analysis Jun 23, 2022 G156812
H2428046 Certificate of Analysis Jun 23, 2022 G156812
I2202561 Certificate of Analysis Jun 23, 2022 G156812
I2202562 Certificate of Analysis Jun 23, 2022 G156812
I2202558 Certificate of Analysis Jun 23, 2022 G156812
G1825227 Certificate of Analysis May 09, 2022 G156812

Show more⌵

Chemical and Physical Properties

Sensitivity Moisture sensitive;Air sensitive
Refractive Index n20/D1.4720 to 1.475
Flash Point(°F) 122 °F
Flash Point(°C) 56°C(lit.)
Boil Point(°C) 183°C(lit.)
Molecular Weight 136.230 g/mol
XLogP3 2.800
Hydrogen Bond Donor Count 0
Hydrogen Bond Acceptor Count 0
Rotatable Bond Count 1
Exact Mass 136.125 Da
Monoisotopic Mass 136.125 Da
Topological Polar Surface Area 0.000 Ų
Heavy Atom Count 10
Formal Charge 0
Complexity 170.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 0
Covalently-Bonded Unit Count 1

Citations of This Product

How to Cite Aladdin Scientific Products?
1. Yaling Huang, Junwen Wan, Min Sun, Tao Feng, Qian Liu, Shiqing Song, Xiaoming Zhang, Chi-Tang Ho.  (2023)  Flavor profile disclosure of Chinese steamed breads (CSBs) by sensomics approach.  Food Bioscience,  51  (102198). 
2. Xiangying Yu, Xiaochun Chen, Yuting Li, Lin Li.  (2022)  Effect of Drying Methods on Volatile Compounds of Citrus reticulata Ponkan and Chachi Peels as Characterized by GC-MS and GC-IMS.  Foods,  11  (17): (2662). 
3. Fulin Li, Lihong Deng, Qiwei Xu, Ke Yuan, Hang Song.  (2022)  Extractive separation of 1,8-cineole and γ-terpinene with lactic acid-based deep eutectic solvents.  JOURNAL OF MOLECULAR LIQUIDS,  363  (119828). 
4. Chengyu Zheng, Qin'an Zhou, Wenqing Shao, Jing Zhang, Jun Wang.  (2022)  Early identification of fungal leaf blight disease (Alternaria alternate) on Platycladus orientalis plants by using gas chromatography-ion mobility spectrometry.  MICROCHEMICAL JOURNAL,  179  (107505). 
5. Ke Yuan, Fulin Li, Lincai Peng, Xiaomeng Zhao, Hang Song.  (2022)  Separation of 1,8-Cineole and terpenes by Liquid-liquid extraction with green alkanediols.  JOURNAL OF MOLECULAR LIQUIDS,  350  (118516). 
6. Zhenhe Wang, Wei Chen, Shuang Gu, Jun Wang, Yongwei Wang.  (2020)  Discrimination of wood borers infested Platycladus orientalis trunks using quartz crystal microbalance gas sensor array.  SENSORS AND ACTUATORS B-CHEMICAL,  309  (127767). 
7. Huijuan Zhang,Jiefen Cui,Guifang Tian,Christina DiMarco-Crook,Wei Gao,Chengying Zhao,Genyuan Li,Yunhe Lian,Hang Xiao,Jinkai Zheng.  (2019-04-09)  Efficiency of four different dietary preparation methods in extracting functional compounds from dried tangerine peel..  Food chemistry,  289  (340-350). 
8. Yuchen Bai, Ningke You, Hongyu Tian, Xuebing Zhao.  (2025)  Characterization of Key Odorants in Hemp Seed Oil Extracted from the Hemp Seeds Roasted Under Various Conditions.  Processes,  13  (2): (530). 
9. Wenyi Duan, Zhenyu Yao, Chengkui Qiao, Junren Meng, Shihang Sun, Lei Pan, Liang Niu, Guochao Cui, Zhiqiang Wang, Wenfang Zeng.  (2025)  Combined volatile metabolome and transcriptome analysis of 60 peach cultivars provide new insights into the formation of aroma and the identification of associated genes.  Horticultural Plant Journal,     
10. Xinming Chen, Dandan Yang, Lin Huang, Mengqi Li, Jihai Gao, Can Liu, Xiaoming Bao, Zhizhi Huang, Jinhui Yang, Haozhou Huang, Dingkun Zhang, Runchun Xu.  (2024)  Comparison and identification of aroma components in 21 kinds of frankincense with variety and region based on the odor intensity characteristic spectrum constructed by HS–SPME–GC–MS combined with E-nose.  FOOD RESEARCH INTERNATIONAL,  195  (114942). 
11. Xiaoming Zeng, Hao He, Liejiang Yuan, Haizhi Wu, Cong Zhou.  (2024)  Determination of 24 Trace Aromatic Substances in Rosemary Hydrosol by Dispersed Liquid–Liquid Microextraction–Gas Chromatography.  Processes,  12  (3): (498). 
12. Yimeng Ren, Longzhu Zhou, Yujie Shi, Yanan Yu, Weihai Xing, Qingyu Zhao, Junmin Zhang, Yueyu Bai, Jing Li, Chaohua Tang.  (2024)  Effect of alterations in phospholipids and free fatty acids on aroma-active compounds in instant-boiled chuck tender, sirloin and silverside beef.  Heliyon,  10   
13. Yuyan Wei, Ling Xie, Bertrand Muhoza, Qian Liu, Shiqing Song.  (2024)  Generation of Olfactory Compounds in Cat Food Attractants: Chicken Liver-Derived Protein Hydrolysates and Their Contribution to Enhancing Palatability.  JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY,  72  (28): (15906-15919). 
14. Suqi Liu, Linjiang Pang, Xiaowei Wu, Shihao Chen, Mingyi Yang, Jiyu Cheng, Guoquan Lu, Zhenhe Wang, Wei Chen, Yuge Guan, Xinghua Lu.  (2024)  Non-destructive detection of trans-caryophyllene in early sweetpotato black spot disease using a QCM gas sensor based on modified CAU-1@ZIF-8 composite.  MICROCHEMICAL JOURNAL,  202  (110782). 
15. Suqi Liu, Xiaowei Wu, Shihao Chen, Cong Liu, Wanqi Zhang, Mingyi Yang, Jiyu Cheng, Guoquan Lu, Zhenhe Wang, Wei Chen, Yuge Guan, Linjiang Pang, Xinghua Lu.  (2025)  Rapid detection of linalool by QCM gas sensor based on HKUST-1/MWCNT-gel@MIP in early sweetpotato black spot disease.  MICROCHEMICAL JOURNAL,  212  (113232). 
16. Zhang Hanchen, Montesdeoca Nicolás, Tang Dongsheng, Liang Ganghao, Cui Minhui, Xu Chun, Servos Lisa-Marie, Bing Tiejun, Papadopoulos Zisis, Shen Meifang, Xiao Haihua, Yu Yingjie, Karges Johannes.  (2024)  Tumor-targeted glutathione oxidation catalysis with ruthenium nanoreactors against hypoxic osteosarcoma.  Nature Communications,  15  (1): (1-23). 

Solution Calculators

Reviews

Customer Reviews

Shall we send you a message when we have discounts available?

Remind me later

Thank you! Please check your email inbox to confirm.

Oops! Notifications are disabled.

Privacy Policy Website Terms of Use Return policy Terms and Conditions of Sale Cookie Policy Sales Policy
Products are chemical reagents for research use only and are not intended for human use. We do not sell to patients.
Copyright © 2023-present Aladdin Scientific Corp . All rights reserved.