PERUVOSIDE
Peruvoside
CAS: 1182-87-2
Molecular Formula: C30H44O9
PERUVOSIDE - Names and Identifiers
PERUVOSIDE - Physico-chemical Properties
| Molecular Formula | C30H44O9 |
| Molar Mass | 548.66 |
| Density | 1.1277 (rough estimate) |
| Melting Point | 161-164°C |
| Boling Point | 540.83°C (rough estimate) |
| Specific Rotation(α) | D22 -71.7° (c = 1.54 in methanol) |
| Solubility | chloroform, methanol, dimethyl sulfoxide |
| Appearance | light yellow(powder) |
| Color | light yellow |
| Storage Condition | 2-8°C |
| Refractive Index | 1.5500 (estimate) |
| MDL | MFCD00133752 |
PERUVOSIDE - Risk and Safety
| Hazard Symbols | T - Toxic |
| Risk Codes | 23/24/25 - Toxic by inhalation, in contact with skin and if swallowed. |
| Safety Description | S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection. S45 - In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.) |
| WGK Germany | 3 |
| RTECS | FH4915000 |
PERUVOSIDE - Introduction
Peruvoside(Peruvoside) is a naturally occurring hypoxanthine compound commonly found in a resin known as Bruce Yahuang balsam (Peruvian balsam). It has the following properties:
1. Appearance: Peruvoside is a yellow solid substance.
2. Solubility: Peruvoside is insoluble in water, but soluble in polar organic solvents such as methanol and ethanol.
3. Stability: Peruvoside is relatively stable at room temperature, but may degrade under high temperature, sun exposure or strong oxidation conditions.
Peruvoside has certain applications in the pharmaceutical industry, mainly used in the following areas:
1. Anti-inflammatory effect: Peruvoside can play an anti-inflammatory effect by inhibiting the activation of inflammatory cells and the release of cytokines.
2. Antibacterial effect: Peruvoside has a certain inhibitory effect on the growth of bacteria and can be used for the treatment of some bacterial infections.
3. Anti-tumor effect: Peruvoside has an inhibitory effect on some tumor cells and may have some potential for tumor treatment.
There are two main methods for the preparation of Peruvoside:
1. Extraction from Bruce sub-yellow clip: Bruce sub-yellow clip contains Peruvoside, which can be obtained by solvent extraction and purification.
2. Synthesis: Peruvoside can also be obtained by chemical synthesis, including various reaction steps and synthetic routes.
When using Peruvoside, you need to pay attention to some safety information:
1. Toxicity: Peruvoside may be toxic at a certain concentration and needs to be used and handled correctly to avoid contact with skin and inhalation.
2. Environmental impact: The discharge and treatment of Peruvoside in the environment should comply with local environmental regulations to avoid environmental pollution.
3. Storage and transportation: Peruvoside should be stored in a cool, dry place, away from fire and oxidant, and avoid violent vibration and collision.
In summary, Peruvoside is a hypoxanthine compound with anti-inflammatory, antibacterial and anti-tumor effects, and has certain application potential in the field of medicine. When using and handling, it is necessary to follow the safety operation specifications to ensure personal safety and environmental protection.
1. Appearance: Peruvoside is a yellow solid substance.
2. Solubility: Peruvoside is insoluble in water, but soluble in polar organic solvents such as methanol and ethanol.
3. Stability: Peruvoside is relatively stable at room temperature, but may degrade under high temperature, sun exposure or strong oxidation conditions.
Peruvoside has certain applications in the pharmaceutical industry, mainly used in the following areas:
1. Anti-inflammatory effect: Peruvoside can play an anti-inflammatory effect by inhibiting the activation of inflammatory cells and the release of cytokines.
2. Antibacterial effect: Peruvoside has a certain inhibitory effect on the growth of bacteria and can be used for the treatment of some bacterial infections.
3. Anti-tumor effect: Peruvoside has an inhibitory effect on some tumor cells and may have some potential for tumor treatment.
There are two main methods for the preparation of Peruvoside:
1. Extraction from Bruce sub-yellow clip: Bruce sub-yellow clip contains Peruvoside, which can be obtained by solvent extraction and purification.
2. Synthesis: Peruvoside can also be obtained by chemical synthesis, including various reaction steps and synthetic routes.
When using Peruvoside, you need to pay attention to some safety information:
1. Toxicity: Peruvoside may be toxic at a certain concentration and needs to be used and handled correctly to avoid contact with skin and inhalation.
2. Environmental impact: The discharge and treatment of Peruvoside in the environment should comply with local environmental regulations to avoid environmental pollution.
3. Storage and transportation: Peruvoside should be stored in a cool, dry place, away from fire and oxidant, and avoid violent vibration and collision.
In summary, Peruvoside is a hypoxanthine compound with anti-inflammatory, antibacterial and anti-tumor effects, and has certain application potential in the field of medicine. When using and handling, it is necessary to follow the safety operation specifications to ensure personal safety and environmental protection.
Last Update：2024-04-09 21:21:28
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Product Name: Peruvoside Visit Supplier Webpage Request for quotationCAS: 1182-87-2
Tel: 609-228-6898
Email: sales@medchemexpress.com
tech@medchemexpress.com
Mobile: 609-228-6898
Spot supply
Product Name: Peruvoside Visit Supplier Webpage Request for quotationCAS: 1182-87-2
Tel: +86-400-900-4166
Email: product@acmec-e.com
Mobile: +86-18621343501
QQ: 2881950922
Wechat: 18621343501
WhatsApp: +86-18621343501
Product Name: Peruvoside Visit Supplier Webpage Request for quotation
CAS: 1182-87-2
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409
CAS: 1182-87-2
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409
View History
PERUVOSIDE
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5-[(2,4-二氟苯氧基)甲基]-糠酸
ANTI-MOUSE GLUCOCORTICOID-INDUCED TNF RECEPTOR EXTRACELLULAR DOMAIN, BIOTIN
6Α-甲基氢化- 二羟基-3,11,20-三酮-21-丁二酸单酯
2,2,3-三氟-3-(三氟甲基)环氧乙烷
乙酰基三氟甲基苯基缬氨酰甘氨酸