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2418-52-2

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2418-52-2 Usage

Description

D-THREITOL, also known as Threitol, is a naturally occurring polyol (sugar alcohol) that can be found in various fruits, plants, and microorganisms. It is a white to light yellow crystalline powder and is one of the major components of the extract of fruiting bodies of Hericium erinaceus, a type of edible mushroom. D-THREITOL possesses unique chemical properties that make it a valuable compound for various applications.

Uses

Used in Pharmaceutical Industry:
D-THREITOL is used as a pharmaceutical compound for its potential therapeutic effects. It has been found to have beneficial properties for human health, including antioxidant and anti-inflammatory activities. Its presence in the extract of Hericium erinaceus, a mushroom known for its medicinal properties, suggests that D-THREITOL may contribute to the overall health benefits of this mushroom.
Used in Food Industry:
D-THREITOL is used as a natural sweetener and humectant in the food industry. Its sugar alcohol properties make it a suitable ingredient for low-calorie and sugar-free products, as it provides sweetness without the negative effects associated with high sugar consumption. Additionally, its ability to retain moisture can help improve the texture and shelf life of various food products.
Used in Cosmetics Industry:
D-THREITOL is used as a moisturizing agent in the cosmetics industry. Its hygroscopic nature allows it to help maintain the skin's moisture balance, making it a valuable ingredient in skincare products. It can be found in various formulations, such as creams, lotions, and serums, to provide hydration and improve the overall appearance of the skin.
Used in Chemical Synthesis:
D-THREITOL is used as a starting material or intermediate in the synthesis of various chemicals and pharmaceuticals. Its unique chemical structure makes it a versatile building block for the development of new compounds with potential applications in different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 2418-52-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,1 and 8 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2418-52:
(6*2)+(5*4)+(4*1)+(3*8)+(2*5)+(1*2)=72
72 % 10 = 2
So 2418-52-2 is a valid CAS Registry Number.

2418-52-2 Well-known Company Product Price

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  • Aldrich

  • (377619)  D-Threitol  99%

  • 2418-52-2

  • 377619-250MG

  • 696.15CNY

  • Detail

2418-52-2SDS

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 D-threitol

1.2 Other means of identification

Product number -
Other names D-THREITOL

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:2418-52-2 SDS

2418-52-2Relevant articles and documents

Product Control and Insight into Conversion of C6 Aldose Toward C2, C4 and C6 Alditols in One-Pot Retro-Aldol Condensation and Hydrogenation Processes

Gao, Lou,Hou, Wenrong,Hui, Yingshuang,Tang, Yi,Zhan, Yulu,Zhang, Yahong

, p. 560 - 566 (2021/06/25)

Alcohols have a wide range of applicability, and their functions vary with the carbon numbers. C6 and C4 alditols are alternative of sweetener, as well as significant pharmaceutical and chemical intermediates, which are mainly obtained through the fermentation of microorganism currently. Similarly, as a bulk chemical, C2 alditol plays a decisive role in chemical synthesis. However, among them, few works have been focused on the chemical production of C4 alditol yet due to its difficult accumulation. In this paper, under a static and semi-flowing procedure, we have achieved the product control during the conversion of C6 aldose toward C6 alditol, C4 alditol and C2 alditol, respectively. About C4 alditol yield of 20 % and C4 plus C6 alditols yield of 60 % are acquired in the one-pot conversion via a cascade retro-aldol condensation and hydrogenation process. Furthermore, in the semi-flowing condition, the yield of ethylene glycol is up to 73 % thanks to its low instantaneous concentration.

Hydrogenolysis of sorbitol into valuable C3-C2 alcohols at low H2 pressure promoted by the heterogeneous Pd/Fe3O4 catalyst

Gumina, Bianca,Mauriello, Francesco,Pietropaolo, Rosario,Galvagno, Signorino,Espro, Claudia

, p. 152 - 160 (2018/02/17)

The hydrogenolysis of sorbitol and various C5-C3 polyols (xylitol; erythritol; 1,2- 1,4- and 2,3-butandiol; 1,2-propandiol; glycerol) have been investigated at low molecular hydrogen pressure (5 bar) by using Pd/Fe3O4, as heterogeneous catalyst and water as the reaction medium. Catalytic experiments show that the carbon chain of polyols is initially shortened through dehydrogenation/decarbonylation and dehydrogenation/retro-aldol mechanisms followed by a series of cascade reactions that include dehydrogenation/decarbonylation and dehydration/hydrogenation processes. At 240 °C, sorbitol is fully converted into lower alcohols with ethanol being the main reaction product in liquid phase.

Effect of tungsten surface density of WO3-ZrO2 on its catalytic performance in hydrogenolysis of cellulose to ethylene glycol

Chai, Jiachun,Zhu, Shanhui,Cen, Youliang,Guo, Jing,Wang, Jianguo,Fan, Weibin

, p. 8567 - 8574 (2017/02/10)

One-pot hydrogenolysis of cellulose to ethylene glycol (EG) was carried out on WO3-based catalysts combined with Ru/C. To probe the active catalytic site for breaking the C-C bond of cellulose, a series of WO3-ZrO2 (WZr) catalysts were synthesized and systematically characterized with XRD, Raman, UV-Vis, H2-TPR, DRIFS and XPS techniques and N2 physisorption experiment. It was found that the WO3 crystallites became more easily reduced to W5+-OH species with increasing crystallite size or tungsten surface density of the WZr catalyst owing to the decrease of their absorption edge energy (AEE) originating from weakening their interaction with ZrO2 support. This, as a result, gave higher EG yield at higher tungsten surface density. The structure-activity relationship of the WZr catalyst reveals that the active catalytic site for cleaving the C2-C3 bond of the glucose molecule is the W5+-OH species.

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