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ROOIBOS EXTRACT ASPALATHUS LINEARIS, also known as "Red Bush" extract, is derived from the Aspalathus Linearis plant, a shrub native to South Africa. It is widely used due to its rich antioxidant content, which includes two unique flavonoids, Aspalathin and Nothofagin, not found in any other plant. This extract is known for its anti-inflammatory, antimutagenic, and antiviral properties. It is caffeine-free, low in tannins, and high in minerals such as calcium, potassium, and zinc. Additionally, it contains alpha hydroxy acid, which is known for promoting healthy skin.

6027-43-6

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6027-43-6 Usage

Uses

Used in Skincare Products:
ROOIBOS EXTRACT ASPALATHUS LINEARIS is used as an active ingredient for its antioxidant, anti-inflammatory, and skin health-promoting properties. It helps to protect the skin from environmental stressors, reduce inflammation, and promote a healthy, youthful appearance.
Used in Health Supplements:
ROOIBOS EXTRACT ASPALATHUS LINEARIS is used as a dietary supplement for its antioxidant, anti-inflammatory, and antimutagenic qualities. It supports overall health by neutralizing free radicals, reducing inflammation, and potentially preventing cellular damage.
Used in Tea:
ROOIBOS EXTRACT ASPALATHUS LINEARIS is used as a tea ingredient for its caffeine-free, low-tannin, and mineral-rich properties. It provides a refreshing and healthful beverage option, with potential health benefits due to its antioxidant and anti-inflammatory properties.

Check Digit Verification of cas no

The CAS Registry Mumber 6027-43-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,2 and 7 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6027-43:
(6*6)+(5*0)+(4*2)+(3*7)+(2*4)+(1*3)=76
76 % 10 = 6
So 6027-43-6 is a valid CAS Registry Number.

6027-43-6 Well-known Company Product Price

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  • Sigma-Aldrich

  • (03520585)  Aspalathin  primary pharmaceutical reference standard

  • 6027-43-6

  • 03520585-10MG

  • 6,803.55CNY

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6027-43-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(3,4-dihydroxyphenyl)-1-[2,4-dihydroxy-5-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]phenyl]propan-1-one

1.2 Other means of identification

Product number -
Other names 2',3,4,4',6'-pentahydroxydihydrochalcone-3'-C-glucoside

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:6027-43-6 SDS

6027-43-6Downstream Products

6027-43-6Relevant academic research and scientific papers

Method for the Synthesis of Aspalathin and Analogues Thereof

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Paragraph 0076; 0077; 0078; 0079; 0080; 0081; 0082, (2013/03/26)

A method of synthesising Aspalathin and its analogues or derivatives is disclosed. The method comprises synthesising a compound of formula 1 or its analogues or derivatives: wherein each of R1, R2, R3, R4, Rsub

METHOD FOR THE SYNTHESIS OF ASPALATHIN AND ANALOGUES THEREOF

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Page/Page column 27, (2011/06/23)

A method of synthesising Aspalathin and its analogues or derivatives is disclosed. The method comprises synthesising a compound of formula 1 or its analogues or derivatives (I) wherein each of R1, R2, R3, R4, R

Concise total syntheses of aspalathin and nothofagin

Yepremyan, Akop,Salehani, Baback,Minehan, Thomas G.

supporting information; experimental part, p. 1580 - 1583 (2010/06/17)

Chemical Fig. Reprentation Syntheses of the C-glycosyl flavone natural products aspalathin and nothofagin have been accomplished in eight steps from tribenzyl glucal, tribenzylphloroglucinol, and either 4-(benzyloxy) phenylacetylene or 3,4-bis(benzyloxy)phenylacetylene. The key step of the syntheses involves a highly stereoselective Lewis acid promoted coupling of 1,2-di-o-acyl-3,4,6-tribenzylglucose with tribenzylphloroglucinol, which gives rise to the corresponding β-C-aryl glycoside in 30-65% yields.

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