Cas no 122-48-5 (Zingerone)
Zingerone Chemical and Physical Properties
Names and Identifiers
-
- zingerone
- Vanillylacetone
- 4-(4-Hydroxy-3-methoxyphenyl)butan-2-one
- 4-(4-Hydroxy-3-methoxyphenyl)-2-butanone
- 2-Butanone,4-(4-hydroxy-3-methoxyphenyl)-
- ZINGERONE(P)
- Gingerone
- FEMA 3124
- Zingarone
- NSC 15335
- zingherone
- [0]-Paradol
- (0)-paradol
- ZINGIBERONE
- Vanillyl acetone
- 2-Butanone, 4-(4-hydroxy-3-methoxyphenyl)-
- 4-Hydroxy-3-methoxybenzylacetone
- (4-Hydroxy-3-methoxyphenyl)ethyl methyl ketone
- 3-Methoxy-4-hydroxybenzylacetone
- 4-(3-Methoxy-4-hydroxyphenyl)-2-butanone
- 3-Methoxy-4-hydroxy-benzylacetone
- FEMA No. 3124
- 2-(4-Hydroxy-3-methoxyphenyl)ethyl methyl k
- Zingerone
-
- MDL: MFCD00048232
- Inchi: 1S/C11H14O3/c1-8(12)3-4-9-5-6-10(13)11(7-9)14-2/h5-7,13H,3-4H2,1-2H3
- InChI Key: OJYLAHXKWMRDGS-UHFFFAOYSA-N
- SMILES: COC1C(O)=CC=C(CCC(=O)C)C=1
Computed Properties
- Exact Mass: 194.09400
- Monoisotopic Mass: 194.094294304 g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 3
- Heavy Atom Count: 14
- Rotatable Bond Count: 4
- Complexity: 191
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- Surface Charge: 0
- Tautomer Count: 9
- XLogP3: 0.8
- Topological Polar Surface Area: 46.5
- Molecular Weight: 194.23
Experimental Properties
- Color/Form: Powder
- Density: 1.14?g/mL?at 25?°C(lit.)
- Melting Point: 40-41?°C (lit.)
- Boiling Point: 141?°C/0.5?mmHg(lit.)
- Flash Point: >110 oC
- Refractive Index: n20/D 1.541(lit.)
- Solubility: Sparingly sol in water, petroleum ether; sol in ether, dil alkalies
- PSA: 46.53000
- LogP: 1.92240
- Odor: STRONG, PUNGENT ODOR REMINISCENT OF GINGER
- Refractive Index: INDEX OF REFRACTION: 1.5440-1.5450 @ 20 °C/D
- FEMA: 3124
- Merck: 10166
Zingerone Security Information
- Prompt:warning
- Hazard Statement: H303
- Warning Statement: P312
- Hazardous Material transportation number:NONH for all modes of transport
- WGK Germany:2
- Hazard Category Code: R36/37/38: irritating to eyes, respiratory tract and skin
- Safety Instruction: S26-S36
- RTECS:EL8900000
- TSCA:Yes
- Storage Condition:4°C, sealed storage, away from moisture
- Safety Term:4.1
- Packing Group:II; III
- Risk Phrases:R36/37/38
Zingerone Customs Data
- HS CODE:29333999
- Customs Data:
China Customs Code:
2914509090Overview:
2914509090 Ketones containing other oxygen-containing groups. VAT:17.0% Tax refund rate:9.0% Regulatory conditions:nothing MFN tariff:5.5% general tariff:30.0%
Declaration elements:
Product Name, component content, use to, Acetone declared packaging
Summary:
HS:2914509090 other ketones with other oxygen function VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:5.5% General tariff:30.0%
Zingerone Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| TI XI AI ( SHANG HAI ) HUA CHENG GONG YE FA ZHAN Co., Ltd. | H1314-100G |
4-(4-Hydroxy-3-methoxyphenyl)-2-butanone |
122-48-5 | >98.0%(GC) | 100g |
¥220.00 | 2024-04-18 | |
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | V117528-100g |
Zingerone |
122-48-5 | 97%, | 100g |
¥541.90 | 2023-08-31 | |
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | V117528-25g |
Zingerone |
122-48-5 | 97%, | 25g |
¥201.90 | 2023-08-31 | |
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | V117528-500g |
Zingerone |
122-48-5 | 97%, | 500g |
¥2410.90 | 2023-08-31 | |
| Chemenu | CM100402-500g |
4-(4-hydroxy-3-methoxyphenyl)butan-2-one |
122-48-5 | 95+% | 500g |
$337 | 2021-06-17 | |
| S e l l e c k ZHONG GUO | S2371-50mg |
Vanillylacetone |
122-48-5 | 99.89% | 50mg |
¥786.58 | 2023-09-15 | |
| HE FEI BO MEI SHENG WU KE JI YOU XIAN ZE REN GONG SI | JV6244-1g |
Zingerone |
122-48-5 | ≥98% | 1g |
¥220元 | 2023-09-15 | |
| HE FEI BO MEI SHENG WU KE JI YOU XIAN ZE REN GONG SI | JV6244-25g |
Zingerone |
122-48-5 | ≥98% | 25g |
¥750元 | 2023-09-15 | |
| HE FEI BO MEI SHENG WU KE JI YOU XIAN ZE REN GONG SI | JV6244-5g |
Zingerone |
122-48-5 | ≥98% | 5g |
¥450元 | 2023-09-15 | |
| HE FEI BO MEI SHENG WU KE JI YOU XIAN ZE REN GONG SI | BZP0852-20mg |
Zingerone |
122-48-5 | HPLC≥98% | 20mg |
¥180元 | 2023-09-15 |
Zingerone Suppliers
Zingerone Related Literature
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Andrea Temperini,Marco Ballarotto,Carlo Siciliano RSC Adv. 2020 10 33706
-
2. Natural products in agarwood and Aquilaria plants: chemistry, biological activities and biosynthesisWei Li,Hui-Qin Chen,Hao Wang,Wen-Li Mei,Hao-Fu Dai Nat. Prod. Rep. 2021 38 528
-
Kunchpillai Lakshmanan Hemalatha,Ponnian Stanely Mainzen Prince RSC Adv. 2016 6 112332
-
James Perkins,Tobias Hayashi,Rod Peakall,Gavin R. Flematti,Bj?rn Bohman Nat. Prod. Rep. 2023 40 819
-
Yingjie Zhu,Chunyan Wang,Jingjing Luo,Shucheng Hua,Dan Li,Liping Peng,Hongmei Liu,Lei Song Food Funct. 2021 12 3120
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Additional information on Zingerone
Zingerone and CAS No 122-48-5: A Comprehensive Overview of Their Chemical Properties and Emerging Applications
The compound Zingerone, identified by the chemical formula CAS No 122-48-5, has garnered significant attention in the field of chemobiology due to its multifaceted pharmacological properties. This heterocyclic compound, belonging to the pyrazole class, exhibits a broad spectrum of biological activities that have positioned it as a promising candidate for therapeutic applications. The structural uniqueness of Zingerone contributes to its distinctive interaction with biological targets, making it a subject of extensive research in both academic and industrial settings.
Zingerone is primarily known for its role as a bioactive compound derived from ginger, specifically from the ginger plant (*Zingiber officinale*). Its chemical structure comprises a pyrazole ring fused with a thiophene ring, which is flanked by hydroxyl and methoxy substituents. This arrangement imparts upon Zingerone the ability to engage with various enzymatic and cellular pathways, thereby influencing metabolic processes and inflammatory responses. The compound’s stability under physiological conditions enhances its suitability for formulation in pharmaceutical products.
Recent advancements in the study of Zingerone have highlighted its potential in modulating oxidative stress and inflammation. Research has demonstrated that Zingerone can inhibit the activity of key enzymes such as lipoxygenase and cyclooxygenase, which are pivotal in the pathogenesis of chronic inflammatory diseases. Moreover, studies have revealed that Zingerone exerts antioxidant effects by scavenging reactive oxygen species (ROS), thereby protecting cells from oxidative damage. These findings align with the growing interest in natural compounds that can ameliorate oxidative stress-related disorders.
The therapeutic implications of Zingerone extend beyond anti-inflammatory and antioxidant actions. Emerging research indicates that Zingerone may possess anticancer properties by inducing apoptosis in cancer cells while sparing healthy cells. Mechanistic studies have shown that Zingerone can activate stress signaling pathways such as p53, leading to the arrest of cell cycle progression and programmed cell death. Additionally, its ability to disrupt microtubule formation has been observed in certain cancer cell lines, further supporting its potential as an anticancer agent.
In the realm of metabolic disorders, Zingerone has shown promise in regulating blood sugar levels and improving insulin sensitivity. Preclinical studies have demonstrated that administration of Zingerone can enhance glucose uptake in adipose tissues and skeletal muscles, thereby mitigating hyperglycemia. Furthermore, its role in modulating lipid metabolism has been explored, with evidence suggesting that Zingerone can reduce triglyceride levels and improve cholesterol profiles. These findings underscore the potential of Zingerone as a therapeutic agent for metabolic syndrome.
The pharmacokinetic profile of Zingerone, as defined by its CAS No 122-48-5, is another area of active investigation. Studies have indicated that Zingerone exhibits good oral bioavailability and distributes widely throughout various tissues upon administration. Its metabolic pathways involve conjugation with glucuronic acid and sulfate groups, which facilitate its excretion via bile and urine. Understanding these pharmacokinetic characteristics is crucial for optimizing dosing regimens and formulation strategies to enhance therapeutic efficacy.
Industrial applications of Zingerone, particularly in nutraceuticals and functional foods, have also gained traction due to its perceived health benefits. The compound’s natural origin from ginger makes it an attractive ingredient for health supplements aimed at promoting well-being and disease prevention. Furthermore, its stability under processing conditions ensures that it can be incorporated into various food products without significant degradation.
Future directions in the research of Zingerone include exploring its synergistic effects when combined with other bioactive compounds or pharmaceutical agents. Additionally, investigating its long-term safety profile will be essential for translating preclinical findings into clinical applications. Collaborative efforts between academia and industry are likely to drive innovation in developing novel derivatives of Zingerone with enhanced pharmacological properties.
In conclusion, Zingerone (CAS No 122-48-5) stands out as a versatile compound with significant therapeutic potential across multiple disease domains. Its unique chemical structure enables it to interact with diverse biological targets, contributing to its wide range of biological activities. As research continues to uncover new mechanisms of action and applications, Zingerone is poised to play an increasingly important role in modern medicine and healthcare solutions.
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