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Arbutin pentaacetate, a derivative of arbutin, is a natural compound found in various plant species, including bearberry plants. It is a more stable form of arbutin, known for its skin-lightening and brightening properties, as well as its ability to inhibit melanin production, reduce the appearance of dark spots and hyperpigmentation, and exhibit antioxidant properties. Arbutin pentaacetate is considered safe for use in skincare products when used at the recommended concentrations.

14698-56-7

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14698-56-7 Usage

Uses

Used in Skincare Industry:
Arbutin pentaacetate is used as a skin-lightening and brightening agent for its ability to inhibit melanin production, which helps reduce the appearance of dark spots and hyperpigmentation.
Used in Anti-Aging Products:
Arbutin pentaacetate is used as an antioxidant ingredient in anti-aging products, contributing to its popularity in skincare formulations for its potential to combat signs of aging and promote a youthful appearance.

Check Digit Verification of cas no

The CAS Registry Mumber 14698-56-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,6,9 and 8 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 14698-56:
(7*1)+(6*4)+(5*6)+(4*9)+(3*8)+(2*5)+(1*6)=137
137 % 10 = 7
So 14698-56-7 is a valid CAS Registry Number.

14698-56-7Downstream Products

14698-56-7Relevant academic research and scientific papers

ARBUTIN AND SUCROSE IN THE LEAVES OF THE RESURRECTION PLANT MYROTHAMNUS FLABELLIFOLIA

Suau, Rafael,Cuevas, Ana,Valpuesta, Victoriano,Reid, Michael S.

, p. 2555 - 2556 (1991)

Forty-two per cent of the desiccated leaves of Myrothamnus flabellifolia was extracted in methanol, and contained two major components, sucrose (30percent) and arbutin (65percent).Its arbutin content can probably explain the purported medicinal properties of this plant.By analogy with other desiccation-tolerant organisms, sucrose and arbutin may be partially responsible for the extreme resistance of Myrothamnus to environmental stress.Key Word Index - Myrothamnus flabellifolia; Myrothamnaceae; resurrection plant; arbutin; sucrose.

Preparation method of glucoside and derivatives thereof

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Paragraph 0040; 0042, (2020/04/02)

The invention discloses a preparation method of glucoside and derivatives thereof. According to the method, all hydroxyl groups on a sugar molecule structure are acetylated, a ligand containing phenolic hydroxyl groups is prepared at the same time, then boron trifluoride-diethyl ether is used as a catalyst, the two substances are condensed to obtain tetraacetylated glucoside, and finally acetyl protecting groups are removed to obtain the required glucoside. The method can selectively catalyze hemiacetal hydroxyl of monosaccharide to react with hydroxyl to obtain glucoside, and the product is single. The method is simple in production operation and low in equipment requirement, can be used for synthesizing glucoside and derivatives thereof with similar structures, is green and environment-friendly, and can be used for large-scale production.

Synthesis method for beta-arbutin

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Paragraph 0024; 0025, (2017/10/13)

The invention discloses a synthesis method for beta-arbutin and belongs to the field of synthesis of daily chemical additives. The invention aims to provide a synthesis method of which the yield can reach 81 to 90 percent. According to the method, tetra-acetyl arbutin is acetylated, and then a product is de-acetylated, wherein the tetra-acetyl arbutin is obtained by reaction among penta-acetyl glucopyranose, hydroquinone and derivatives thereof under ionic liquid. The synthesis method for the beta-arbutin can be used for synthesizing the beta-arbutin in daily chemical products.

Effective friedel-crafts acylations of O- and C-arylglycosides with triflic acid

Hashimoto, Makoto,Takahashi, Miho

body text, p. 227 - 231 (2009/09/06)

Triflic acid is well known not only as a Friedel-Crafts promoter, but also as a deglycosidation reagent. In this study, we promote effective Friedel-Crafts acylations for O- or C-arylglucosides without deglycosidation and check their inhibitory activities for β-glucosidase.

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