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Glutinol acetate, a natural chemical compound belonging to the triterpenoid family, is derived from various plant sources, including the resins of black gum and other Nyssa species. It has been studied for its potential biological activities, such as anti-inflammatory, anti-tumor, and anti-cancer properties, making it a promising candidate for the development of new drugs for the treatment of various diseases, particularly those related to inflammation and cancer.

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  • 6426-44-4 Structure
  • Basic information

    1. Product Name: Glutinol acetate
    2. Synonyms: Glutinol acetate;Glutin-5-en-3beta-O-acetate;Glutinyl acetate
    3. CAS NO:6426-44-4
    4. Molecular Formula: C32H52O2
    5. Molecular Weight: 468.75408
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 6426-44-4.mol
  • Chemical Properties

    1. Melting Point: 192℃ (methanol )
    2. Boiling Point: 505.1±29.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.02±0.1 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Glutinol acetate(CAS DataBase Reference)
    10. NIST Chemistry Reference: Glutinol acetate(6426-44-4)
    11. EPA Substance Registry System: Glutinol acetate(6426-44-4)
  • 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: 6426-44-4(Hazardous Substances Data)

6426-44-4 Usage

Uses

Used in Pharmaceutical Industry:
Glutinol acetate is used as a potential therapeutic agent for its anti-inflammatory properties, which can help in the treatment of various inflammatory conditions.
Used in Oncology:
Glutinol acetate is used as an anti-tumor and anti-cancer agent, showing promise in the development of new drugs for the treatment of various types of cancer.
Used in Drug Development:
Glutinol acetate is used as a lead compound in the development of new drugs, particularly for diseases related to inflammation and cancer, due to its potential biological activities and therapeutic potential.
Further research is needed to fully understand the potential benefits and applications of Glutinol acetate, as well as to explore its efficacy and safety in various therapeutic areas.

Check Digit Verification of cas no

The CAS Registry Mumber 6426-44-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,2 and 6 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6426-44:
(6*6)+(5*4)+(4*2)+(3*6)+(2*4)+(1*4)=94
94 % 10 = 4
So 6426-44-4 is a valid CAS Registry Number.

6426-44-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (3S,6aS,6bR,8aR,12aR,12bS,14aR,14bS)-4,4,6b,8a,11,11,12b,14a-octamethyl-1,2,3,4,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14,14a,14b-icosahydropicen-3-yl acetate

1.2 Other means of identification

Product number -
Other names -

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:6426-44-4 SDS

6426-44-4Downstream Products

6426-44-4Relevant articles and documents

13C NMR Spectroscopic Data for Glutinol and Derivatives

Olea, Roberto Sigfrido Gallegos,Torres, Luce Maria Brandao,Roque, Luiz Carlos,Roque, Nidia Franca

, p. 378 - 379 (1994)

The 13C NMR chemical shifts of the triterpenes glutinol, glutinone and acetylglutinol were measured and analysed. - Keywords: 13C NMR Glutinol Glutinone Acetylglutinol

SCHEFFLERIN AND ISOSCHEFFLERIN: PRENYLATED CHALCONES AND OTHER CONSTITUENTS OF UVARIA SCHEFFLERI

Nkunya, Mayunga H. H.,Achenbach, Hans,Renner, Christian,Waibel, Reiner,Weenen, Hugo

, p. 1261 - 1264 (1990)

Two new prenylated chalcones, schefflerin and isoschefflerin, were isolated from the petrol fraction of the ethanol extract of the stem bark of Uvaria scheffleri, in addition to D: B-friedoolean-5-en-3β-ol (= glutin-5-en-3β-ol), 3-farnesylindole, 2'-hydroxy-3',4',6'-trimethoxychalcone, 2',6'-dihydroxy-3',4'-dimethoxychalcone, β-sitosterol and benzyl benzoate.

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