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5487-50-3

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5487-50-3 Usage

Derivation

Derived from pentadecanoic acid, a saturated fatty acid

Common Uses

1. Fragrance or flavoring agent
2. Chemical intermediate in the production of other compounds

Applications

1. Cosmetic and personal care industries (perfumes, soaps, lotions)
2. Synthetic flavors for food and beverages

Potential Pharmaceutical Applications

1. Antibacterial properties
2. Anti-inflammatory properties

Versatility

Wide range of industries

Check Digit Verification of cas no

The CAS Registry Mumber 5487-50-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,8 and 7 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5487-50:
(6*5)+(5*4)+(4*8)+(3*7)+(2*5)+(1*0)=113
113 % 10 = 3
So 5487-50-3 is a valid CAS Registry Number.

5487-50-3SDS

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 methyl 13-methylpentadecanoate

1.2 Other means of identification

Product number -
Other names Pentadecanoic acid,13-methyl-,methyl ester

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:5487-50-3 SDS

5487-50-3Downstream Products

5487-50-3Relevant articles and documents

Mirabolides A and B; new cytotoxic glycerides from the Red Sea sponge Theonella mirabilis

Abou-Hussein, Dina R.,Youssef, Diaa T. A.

, (2016/09/09)

As a part of our continuing work to find out bioactive lead molecules from marine invertebrates, the CHCl3 fraction of the organic extract of the Red Sea sponge Theonella mirabilis showed cytotoxic activity in our primary screen. Bioassay-guided purification of the active fractions of the sponge's extract resulted in the isolation of two new glycerides, mirabolides A and B (1 and 2), together with the reported 4-methylene sterols, conicasterol (3) and swinhosterol B (4). The structures of the compounds were assigned by interpretation of their 1D (1H, 13C), 2D (COSY, HSQC, HMBC, ROESY) NMR spectral data and high-resolution mass determinations. Compounds 1-4 displayed marked cytotoxic activity against human breast adenocarcinoma cell line (MCF-7) with IC50 values of 16.4, 5.18, 6.23 and 3.0 μg/mL, respectively, compared to 5.4 μg/mL observed by doxorubicin as reference drug.

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