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506-50-3

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506-50-3 Usage

Chemical Properties

slightly yellow fluffy crystalline powder

Uses

Different sources of media describe the Uses of 506-50-3 differently. You can refer to the following data:
1. Biochemical research.
2. Triacontanoic Acid has agricultural applications and is a useful compound in the removal of residual pesticides from fruit via ozone-microbubble treatment.
3. Melissic acid was used in a study on identification and determination of very-long-chain polyunsaturated fatty acid in freshwater crustacean species Bathynella natans.

Definition

ChEBI: A C30, very long straight-chain, saturated fatty acid.

General Description

Melissic acid is isolated from the pericarp of Trichosanthes rosthornii.

Check Digit Verification of cas no

The CAS Registry Mumber 506-50-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,0 and 6 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 506-50:
(5*5)+(4*0)+(3*6)+(2*5)+(1*0)=53
53 % 10 = 3
So 506-50-3 is a valid CAS Registry Number.
InChI:InChI=1/C30H60O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-24-25-26-27-28-29-30(31)32/h2-29H2,1H3,(H,31,32)

506-50-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name melissic acid

1.2 Other means of identification

Product number -
Other names Melissic Acid

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:506-50-3 SDS

506-50-3Relevant articles and documents

NON-ALKALOIDAL CONSTITUENTS FROM SOLANIUM TORVUM LEAVES

Mahmood, Umar,Shukla, Yogendra N.,Thakur, Raghunath S.

, p. 167 - 170 (1983)

Three new compounds A, B and C, isolated from the leaves of Solanum torvum have been characterized as 2,3,4-trimethyltriacontane, octacosanyl tricontanoate and 5-hexatricontanone by spectral data and chemical studies.Tricontanol, 3-tricontanone, tetratricontanoic acid, sitosterol, stigmasterol and campesterol have olso been isolated and identified.Key Word Index:Solanum torvum; Solanaceae; leaves; 2,3,4-trimethyltriacontane; octacosanyl triacontanoate; 5-hexatriacontanone; triacontanol; 3-triacontanone; tetratriacontanoic acid; sitosterol; stigmasterol; campesterol

New steroidal glycoside ester and aliphatic acid from the fruits of Lycium Chinense

Jung, Woo-Suk,Chung, Ill-Min,Ali, Mohd,Ahmad, Ateeque

experimental part, p. 301 - 307 (2012/08/28)

Two new compounds stigmast-5-en-3β-ol-3-O-β-D-(2′-n- triacontanoyl) glucopyranoside (1) and 19,21-dimethyl triacont-17,22,24,26,28- pentaene-1-oic acid (2), along with the three known compounds n-tetracosanyl octadec-9-enoate (3), β-sitosterol, and β-sito

Lupeol ester from Clerodendrum phlomidis L.

Pandey,Kaur,Malasoni,Gupta

, p. 470 - 472 (2008/09/21)

A new triterpene ester, together with tetratriacontanol and 24β-ethylcholesta-5,22E,25-triene-3β-ol, has been isolated from the aerial parts of Clerodendrum phlomidis L. Occurrence of a triterpene fatty acid ester lup-20(29)-en-3-triacontanoate in this plant is of taxonomic importance. Structures of all the isolated compounds have been established by spectroscopic and chemical studies.

OZONOLYSIS OF ALKENES AND REACTIONS OF POLYFUNCTIONAL COMPOUNDS XLI. SYNTHESIS OF OXYGEN-CONTAINING DERIVATIVES OF TRIACONTANE

Odinokov, V. N.,Akhmetova, V. R.,Khasanov, Kh. D.,Abduvakhabov, A. A.,Tolstikov, G. A.

, p. 1209 - 1210 (2007/10/02)

Triacontanoic acid, its ester, triacontan-1-ol, and also their 12-Z-unsaturated analogs were synthetized on the basis of methyl 12-oxododecenoate, which is the product from ozonolysis of cyclododecene.

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