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Paeonimetabolin I is a natural chemical compound derived from the roots of Paeonia lactiflora, also known as peony. It is a bioactive metabolite that has demonstrated various pharmacological properties, such as anti-inflammatory, antioxidant, and neuroprotective activities. Its potential therapeutic applications in treating inflammatory and neurological disorders make it a promising candidate for further research and development.

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  • 99624-67-6 Structure
  • Basic information

    1. Product Name: paeonimetabolin I
    2. Synonyms: paeonimetabolin I
    3. CAS NO:99624-67-6
    4. Molecular Formula: C10H14O4
    5. Molecular Weight: 198.2158
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 99624-67-6.mol
    9. Article Data: 3
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 323.6°Cat760mmHg
    3. Flash Point: 129.2°C
    4. Appearance: /
    5. Density: 1.371g/cm3
    6. Vapor Pressure: 2.03E-05mmHg at 25°C
    7. Refractive Index: 1.566
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: paeonimetabolin I(CAS DataBase Reference)
    11. NIST Chemistry Reference: paeonimetabolin I(99624-67-6)
    12. EPA Substance Registry System: paeonimetabolin I(99624-67-6)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 99624-67-6(Hazardous Substances Data)

99624-67-6 Usage

Uses

Used in Pharmaceutical Industry:
Paeonimetabolin I is used as a therapeutic agent for its anti-inflammatory properties, targeting the treatment of inflammatory disorders. Its ability to modulate the immune response and reduce oxidative stress contributes to its potential as a treatment option for various inflammatory conditions.
Used in Neurological Applications:
Paeonimetabolin I is used as a neuroprotective agent for its potential to treat neurological disorders. Its neuroprotective activities may help in mitigating the effects of neurodegenerative diseases and promoting the health of the nervous system.
Further research is necessary to fully understand the mechanisms of action and explore the potential clinical uses of Paeonimetabolin I in these applications.

Check Digit Verification of cas no

The CAS Registry Mumber 99624-67-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,6,2 and 4 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 99624-67:
(7*9)+(6*9)+(5*6)+(4*2)+(3*4)+(2*6)+(1*7)=186
186 % 10 = 6
So 99624-67-6 is a valid CAS Registry Number.
InChI:InChI=1/C10H14O4/c1-5-6-3-10(12)9(2,4-7(6)11)13-8(5)14-10/h5-6,8,12H,3-4H2,1-2H3

99624-67-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 7S-paeonimetaboline I

1.2 Other means of identification

Product number -
Other names 7S-paeonimetabolin I

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:99624-67-6 SDS

99624-67-6Relevant articles and documents

Enantiospecific syntheses of paeonilactone A, paeonilactone B, 7S-paeonimetabolin-I, and 7R-paeonimetabolin-I from R-(-)-carvone

Hatakeyama,Kawamura,Shimanuki,Takano

, p. 333 - 336 (2007/10/02)

The first enantiospecific syntheses of the title monoterpenes have been accomplished starting with R-(-)-carvone, which made their absolute structures unequivocal.

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