(S)-(+)-Carvone - 10mM in DMSO , CAS No.2244-16-8

CAS: 2244-16-8 Cat. No.: S422701 Peso molecular: 150.22 Beilstein Registry Number: 2042970 Número EC: 218-827-2
Disponible para pedir
GRADE & PURITY 10mM in DMSO
Synonyms
NCGC00091882-04 | Talent | AM84798 | Carvol | (4S)-p-mentha-1(6),8-dien-2-one | (S)-(+)-Carvone | (5S)-2-methyl-5-(prop-1-en-2-yl)cyclohex-2-en-1-one | DTXSID8020256 | (5S)-2-methyl-5-(1-methylethenyl)-2-cyclohexen-1-one | FEMA NO. 2249, (+)- | Tox21_2014
Storage
Store at -80°C
Shipped In
Dry ice packs + Cold packs
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
1ml
S422701-1ml
1

47,90US$

69,90US$
Guardar 22,00 US$ (31.47%)
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Why this grade

10mM in DMSO for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Store at -80°C Ships Dry ice packs + Cold packs Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 10 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

A terpene standard for gas chromatography.

Specifications

Sinónimos
NCGC00091882-04 | Talent | AM84798 | Carvol | (4S)-p-mentha-1(6), 8-dien-2-one | (S)-(+)-Carvone | (5S)-2-methyl-5-(prop-1-en-2-yl)cyclohex-2-en-1-one | DTXSID8020256 | (5S)-2-methyl-5-(1-methylethenyl)-2-cyclohexen-1-one | FEMA NO. 2249, (+)- | Tox21_2014
Especificaciones y pureza
10mM in DMSO
Mecanismos bioquímicos y fisiológicos
Terpene standard for gas chromatography. TRP channel activator.
Condiciones de almacenamiento de almacenamiento
Store at -80°C
Enviado en
Dry ice packs + Cold packs
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Nombres e identificadores
Sonrisas canónicasCC1=CCC(CC1=O)C(=C)C
IUPAC Name(5S)-2-methyl-5-prop-1-en-2-ylcyclohex-2-en-1-one
InChIKeyULDHMXUKGWMISQ-VIFPVBQESA-N
INCHI1S/C10H14O/c1-7(2)9-5-4-8(3)10(11)6-9/h4,9H,1,5-6H2,2-3H3/t9-/m0/s1
Isómeros SMILES CC1=CC[C@@H](CC1=O)C(=C)C
WGK Alemania 1
RTECS OS8670000
Número ONU 2810
Grupo de embalaje I
Peso molecular 150.22
Beilstein 2042970
Reaxy-Rn 1364206
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1364206&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassLipids and lipid-like molecules
ClasePrenol lipids
SubclassMonoterpenoids
Intermediate Tree Nodes Not available
Direct ParentMenthane monoterpenoids
Alternative Parents Monocyclic monoterpenoids  Cyclohexenones  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAliphatic homomonocyclic compounds
Substituents P-menthane monoterpenoid - Monocyclic monoterpenoid - Cyclohexenone - Cyclic ketone - Ketone - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic homomonocyclic compound
DescripciónThis compound belongs to the class of organic compounds known as menthane monoterpenoids. These are monoterpenoids with a structure based on the o-, m-, or p-menthane backbone. P-menthane consists of the cyclohexane ring with a methyl group and a (2-methyl)-propyl group at the 1 and 4 ring position, respectively. The o- and m- menthanes are much rarer, and presumably arise by alkyl migration of p-menthanes.
External Descriptors Menthane monoterpenoids - Cyclic monoterpenes
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
ACHE Tclin Acetylcholinesterase (18204 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
THRB Tclin Thyroid hormone receptor beta-1 (7926 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ALDH1A1 Tchem Aldehyde dehydrogenase 1A1 (77053 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
RGS4 Tchem Regulator of G-protein signaling 4 (13867 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MEN1 Tchem Menin/Histone-lysine N-methyltransferase MLL (48157 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Objetivos asociados (no humanos)
Plasmodium falciparum (966862 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Candida albicans (78123 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Tribolium castaneum (596 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Nfe2l2 Nuclear factor erythroid 2-related factor 2 (214 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Rorc Nuclear receptor ROR-gamma (89407 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Propiedades químicas y físicas
SensibilidadHygroscopic,Light & Air sensitive.
Índice de refracción1.497
Rotación específica [α]61.5 ° (neat)
Punto de inflamación (°F)192.2 °F
Punto de inflamación (°C)98 °C
Punto de ebullición (°C)230 °C
Peso molecular150.220 g/mol
XLogP32.400
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count1
Rotatable Bond Count1
Exact Mass150.104 Da
Monoisotopic Mass150.104 Da
Topological Polar Surface Area17.100 Ų
Heavy Atom Count11
Formal Charge0
Complexity223.000
Isotope Atom Count0
Defined Atom Stereocenter Count1
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Citations of This Product
Referencias
1. Shijin Wu, Qiang Wang, Xiaojing Ma, Lequan Qiu, Hongde Yan.  (2023)  Modulation of the catalytic performance of OYE3 by engineering key residues at the entrance of the catalytic pocket.  BIOTECHNOLOGY AND APPLIED BIOCHEMISTRY,      [PMID:37073879] [10.1002/bab.2468]
2. Yujiao Cheng, Leng Han, Linhua Huang, Xiang Tan, Houjiu Wu, Guijie Li.  (2023)  Association between flavor composition and sensory profile in thermally processed mandarin juices by multidimensional gas chromatography and multivariate statistical analysis.  FOOD CHEMISTRY,      [PMID:37030207] [10.1016/j.foodchem.2023.136026]
3. Zhuo Liu, Fei Guo, Lei Cheng, Xiangjie Bo, Tingting Liu, Mian Li.  (2022)  Fabrication of manganese borate/iron carbide encapsulated in nitrogen and boron co-doped carbon nanowires as the accelerated alkaline full water splitting bi-functional electrocatalysts.  JOURNAL OF COLLOID AND INTERFACE SCIENCE,      [PMID:36152575] [10.1016/j.jcis.2022.09.068]
4. Zhenyuan Hu, Yunfeng Zhang, Xinyang Long, Wei Bao, Yi Zhang, Weizhen Fan, Hansong Cheng.  (2022)  Hydroxyl-rich single-ion conductors enable solid hybrid polymer electrolytes with excellent compatibility for dendrite-free lithium metal batteries.  JOURNAL OF MEMBRANE SCIENCE,      [PMID:] [10.1016/j.memsci.2022.120666]
5. Zhuo Liu, Fei Guo, Lina Han, Jie Xiao, Xiaoyuan Zeng, Chengxu Zhang, Peng Dong, Mian Li, Yingjie Zhang.  (2022)  Manganese Oxide/Iron Carbide Encapsulated in Nitrogen and Boron Codoped Carbon Nanowire Networks as Accelerated Alkaline Hydrogen Evolution and Oxygen Reduction Bifunctional Electrocatalysts.  ACS Applied Materials & Interfaces,      [PMID:35263074] [10.1021/acsami.1c23731]
6. Yixiang Li, Yajun Bai, Tai-Ping Fan, Xiaohui Zheng, Yujie Cai.  (2021)  Characterization of a putative tropinone reductase from Tarenaya hassleriana with a broad substrate specificity.  BIOTECHNOLOGY AND APPLIED BIOCHEMISTRY,  69  (6): (2530-2539).  [PMID:34902878] [10.1002/bab.2302]
7. Feixu Mo, Xianfeng Hu, Yi Ding, Rongyu Li, Youhua Long, Xiaomao Wu, Ming Li.  (2021)  Naturally produced magnolol can significantly damage the plasma membrane of Rhizoctonia solani.  PESTICIDE BIOCHEMISTRY AND PHYSIOLOGY,      [PMID:34446208] [10.1016/j.pestbp.2021.104942]
8. Guo-Feng Mao, Xiao-Chang Mo, Hatem Fouad, Ghulam Abbas, Jian-Chu Mo.  (2018)  Attraction behaviour of Anagrus nilaparvatae to remote lemongrass (Cymbopogon distans) oil and its volatile compounds.  NATURAL PRODUCT RESEARCH,      [PMID:28503948] [10.1080/14786419.2017.1326486]
9. Shen Song, Yufei Tang, Rui Feng, Xiaohan Zhang, Yue An, Weibao Kong, Junlong Wang, Ji Zhang, Junyu Liang.  (2024)  Bioactivities and Synergistic Effect of Elsholtzia ciliata Essential Oil and Its Main Components against Lasioderma serricorne.  MOLECULES,  29  (9): (1924).  [PMID:38731415] [10.3390/molecules29091924]
10. Yujiao Cheng, Min Zhang, Leng Han, Guijie Li, Min Hong, Hua Wang, Houjiu Wu, Linhua Huang.  (2025)  Investigating the influence of insoluble pulp particles on flavor retention and characterization of freshly squeezed and pasteurized mandarin juice.  FOOD RESEARCH INTERNATIONAL,      [PMID:40263853] [10.1016/j.foodres.2025.116237]
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