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D-Talose, also known as D-threose, is a monosaccharide sugar that can convert between aldose and ketose forms in pyridine in the presence of aluminum oxide. It is characterized by its white fine crystalline powder appearance.

2595-98-4

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2595-98-4 Usage

Uses

Used in Pharmaceutical Industry:
D-Talose is used as an intermediate in the synthesis of various pharmaceutical compounds for its ability to convert between different sugar forms, which can be beneficial in the development of new drugs.
Used in Chemical Industry:
D-Talose is used as a starting material for the production of various organic compounds due to its unique chemical properties, including its ability to convert between aldose and ketose forms.
Used in Research and Development:
D-Talose is used as a research compound for studying the properties and behavior of monosaccharides, as well as their role in various biological processes.
Used in Food Industry:
D-Talose can be used as a sweetener in the food industry, taking advantage of its sugar properties and potential applications in creating new or improved food products.
Used in Cosmetics Industry:
D-Talose may be used in the development of cosmetics and personal care products, leveraging its unique properties to enhance the formulation and performance of these products.

Check Digit Verification of cas no

The CAS Registry Mumber 2595-98-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,9 and 5 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2595-98:
(6*2)+(5*5)+(4*9)+(3*5)+(2*9)+(1*8)=114
114 % 10 = 4
So 2595-98-4 is a valid CAS Registry Number.
InChI:InChI=1/C6H12O6/c7-1-2-3(8)4(9)5(10)6(11)12-2/h2-11H,1H2/t2-,3+,4+,5+,6?/m1/s1

2595-98-4 Well-known Company Product Price

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  • (Code)Product description
  • CAS number
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  • Alfa Aesar

  • (B21226)  alpha-D-(+)-Talose, 97%   

  • 2595-98-4

  • 0.1g

  • 725.0CNY

  • Detail
  • Alfa Aesar

  • (B21226)  alpha-D-(+)-Talose, 97%   

  • 2595-98-4

  • 0.5g

  • 2871.0CNY

  • Detail

2595-98-4SDS

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 aldehydo-D-talose

1.2 Other means of identification

Product number -
Other names D-Talose

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:2595-98-4 SDS

2595-98-4Relevant academic research and scientific papers

Anti-inflammatory active components of the roots of Datura metel

Qin, Ze,Zhang, Jin,Chen, Liang,Liu, Shu-Xiang,Zhao, Hai-Feng,Mao, Hui-Min,Zhang, Hong-Yang,Li, De-Fang

, p. 392 - 398 (2020/03/30)

One new phenolic glycoside, methyl 3,4-dihydroxyphenylacetate-4-O-[2-O-β-D-apisoyl-6-O-(2-hydroxybenzoyl)]-β-D-glucopyranoside (1), together with 10 known compounds (2–11), were isolated from the roots of Datura metel. The structures of these compounds we

Orthogonal Active-Site Labels for Mixed-Linkage endo-β-Glucanases

Jain, Namrata,Tamura, Kazune,Déjean, Guillaume,Van Petegem, Filip,Brumer, Harry

, p. 1968 - 1984 (2021/05/26)

Small molecule irreversible inhibitors are valuable tools for determining catalytically important active-site residues and revealing key details of the specificity, structure, and function of glycoside hydrolases (GHs). β-glucans that contain backbone β(1,3) linkages are widespread in nature, e.g., mixed-linkage β(1,3)/β(1,4)-glucans in the cell walls of higher plants and β(1,3)glucans in yeasts and algae. Commensurate with this ubiquity, a large diversity of mixed-linkage endoglucanases (MLGases, EC 3.2.1.73) and endo-β(1,3)-glucanases (laminarinases, EC 3.2.1.39 and EC 3.2.1.6) have evolved to specifically hydrolyze these polysaccharides, respectively, in environmental niches including the human gut. To facilitate biochemical and structural analysis of these GHs, with a focus on MLGases, we present here the facile chemo-enzymatic synthesis of a library of active-site-directed enzyme inhibitors based on mixed-linkage oligosaccharide scaffolds and N-bromoacetylglycosylamine or 2-fluoro-2-deoxyglycoside warheads. The effectiveness and irreversibility of these inhibitors were tested with exemplar MLGases and an endo-β(1,3)-glucanase. Notably, determination of inhibitor-bound crystal structures of a human-gut microbial MLGase from Glycoside Hydrolase Family 16 revealed.

Method for preparing lactic acid through catalytically converting carbohydrate

-

Paragraph 0029-0040, (2020/11/01)

The invention relates to a method for preparing lactic acid through catalytically converting carbohydrate, and in particular, relates to a process for preparing lactic acid by catalytically convertingcarbohydrate under hydrothermal conditions. The method disclosed by the invention is characterized by specifically comprising the following steps: 1) adding carbohydrate and a catalyst into a closedhigh-pressure reaction kettle, and then adding pure water for mixing; 2) introducing nitrogen into the high-pressure reaction kettle to discharge air, introducing nitrogen of 2 MPa, stirring and heating to 160-300 DEG C, and carrying out reaction for 10-120 minutes; 3) putting the high-pressure reaction kettle in an ice-water bath, and cooling to room temperature; and 4) filtering the solution through a microporous filtering membrane to obtain the target product. The method can realize high conversion rate of carbohydrate and high yield of lactic acid, and has the advantages of less catalyst consumption, good circularity, small corrosion to reaction equipment and the like.

Converting galactose into the rare sugar talose with cellobiose 2-epimerase as biocatalyst

Van Overtveldt, Stevie,Gevaert, Ophelia,Cherlet, Martijn,Beerens, Koen,Desmet, Tom

, (2018/10/20)

Cellobiose 2-epimerase from Rhodothermus marinus (RmCE) reversibly converts a glucose residue to a mannose residue at the reducing end of β-1,4-linked oligosaccharides. In this study, the monosaccharide specificity of RmCE has been mapped and the synthesis of D-talose from D-galactose was discovered, a reaction not yet known to occur in nature. Moreover, the conversion is industrially relevant, as talose and its derivatives have been reported to possess important antimicrobial and anti-inflammatory properties. As the enzyme also catalyzes the keto-aldo isomerization of galactose to tagatose as a minor side reaction, the purity of talose was found to decrease over time. After process optimization, 23 g/L of talose could be obtained with a product purity of 86% and a yield of 8.5% (starting from 4 g (24 mmol) of galactose). However, higher purities and concentrations can be reached by decreasing and increasing the reaction time, respectively. In addition, two engineering attempts have also been performed. First, a mutant library of RmCE was created to try and increase the activity on monosaccharide substrates. Next, two residues from RmCE were introduced in the cellobiose 2-epimerase from Caldicellulosiruptor saccharolyticus (CsCE) (S99M/Q371F), increasing the kcat twofold.

An Effective Heterogeneous Catalyst of [BMIM]3PMo12O40 for Selective Sugar Epimerization

Bayu, Asep,Yoshida, Akihiro,Karnjanakom, Surachai,Zuo, Zhijun,Hao, Xiaogang,Abudula, Abuliti,Guan, Guoqing

, p. 383 - 389 (2018/05/04)

The development of heterogeneous catalysts for the epimerization of sugars has received much less attention than that for the isomerization of sugars. To date, molybdates are the most effective catalysts for the epimerization of sugars, although they lack stability toward hydrolysis of their active sites in water. To solve the issue of the formation of a highly water-soluble heteropolyblue (PMored) for phosphomolybdates (PMos) in aqueous reaction systems, herein, a 1-butyl-3-methylimidazolium phosphomolybdate ([BMIM]3PMo12O40) was synthesized through an ion-exchange method. This catalyst was effective and selective for the C2-epimerization of sugars under mild reaction conditions (red was detected by means of UV/Vis spectroscopy. Moreover, the catalyst can be simply separated by filtration and reused for at least eight cycles without a drop in catalytic activity. XRD, FTIR, and X-ray photoelectron spectroscopy measurements indicate that the catalyst is stable under the reaction conditions. In a comparison of the catalytic activity and surface wettability with those of other PMo salts, that is, 1-ethyl-3-methylimidazolium phosphomolybdate ([EMIM]3PMo12O40), 1-hexyl-3-methylimidazolium ([HexMIM]3PMo12O40), [choline]3PMo12O40, and cetyltrimethylammonium phosphomolybdate ([CTA]3PMo12O40), it is found that [BMIM]3PMo12O40 has more appropriate hydrophobic–hydrophilic balance, which should be responsible for better catalytic activity and stability.

Formation of Chiral Structures in Photoinitiated Formose Reaction

Stovbun,Skoblin,Zanin,Tverdislov,Taran,Parmon

, p. 108 - 116 (2018/04/05)

The possibility to synthesize biologically important sugars and other chiral compounds without any initiators in the UV-initiated reaction of formaldehyde in aqueous solution has been shown for the first time. An optically active condensed phase due to an

Shape-selective Valorization of Biomass-derived Glycolaldehyde using Tin-containing Zeolites

Tolborg, S?ren,Meier, Sebastian,Saravanamurugan, Shunmugavel,Fristrup, Peter,Taarning, Esben,Sádaba, Irantzu

, p. 3054 - 3061 (2016/11/17)

A highly selective self-condensation of glycolaldehyde to different C4 molecules has been achieved using Lewis acidic stannosilicate catalysts in water at moderate temperatures (40–100 °C). The medium-sized zeolite pores (10-membered ring framework) in Sn-MFI facilitate the formation of tetrose sugars while hindering consecutive aldol reactions leading to hexose sugars. High yields of tetrose sugars (74 %) with minor amounts of vinyl glycolic acid (VGA), an α-hydroxyacid, are obtained using Sn-MFI with selectivities towards C4 products reaching 97 %. Tin catalysts having large pores or no pore structure (Sn-Beta, Sn-MCM-41, Sn-SBA-15, tin chloride) led to lower selectivities for C4 sugars due to formation of hexose sugars. In the case of Sn-Beta, VGA is the main product (30 %), illustrating differences in selectivity of the Sn sites in the different frameworks. Under optimized conditions, GA can undergo further conversion, leading to yields of up to 44 % of VGA using Sn-MFI in water. The use of Sn-MFI offers multiple possibilities for valorization of biomass-derived GA in water under mild conditions selectively producing C4 molecules.

Production of keto-disaccharides from aldo-disaccharides in subcritical aqueous ethanol

Gao, Da-Ming,Kobayashi, Takashi,Adachi, Shuji

, p. 998 - 1005 (2016/05/09)

Isomerization of disaccharides (maltose, isomaltose, cellobiose, lactose, melibiose, palatinose, sucrose, and trehalose) was investigated in subcritical aqueous ethanol. A marked increase in the isomerization of aldo-disaccharides to keto-disaccharides was noted and their hydrolytic reactions were suppressed with increasing ethanol concentration. Under any study condition, the maximum yield of keto-disaccharides produced from aldo-disaccharides linked by β-glycosidic bond was higher than that produced from aldo-disaccharides linked by α-glycosidic bond. Palatinose, a keto-disaccharide, mainly underwent decomposition rather than isomerization in subcritical water and subcritical aqueous ethanol. No isomerization was noted for the non-reducing disaccharides trehalose and sucrose. The rate constant of maltose to maltulose isomerization almost doubled by changing solvent from sub-critical water to 80 wt% aqueous ethanol at 220°C. Increased maltose monohydrate concentration in feed decreased the conversion of maltose and the maximum yield of maltulose, but increased the productivity of maltulose. The maximum productivity of maltulose was ca. 41 g/(h kg-solution).

Acid-Assisted Ball Milling of Cellulose as an Efficient Pretreatment Process for the Production of Butyl Glycosides

Boissou, Florent,Sayoud, Nassim,De Oliveira Vigier, Karine,Barakat, Abdellatif,Marinkovic, Sinisa,Estrine, Boris,Jér?me, Fran?ois

, p. 3263 - 3269 (2015/10/19)

Ball milling of cellulose in the presence of a catalytic amount of H2SO4 was found to be a promising pre-treatment process to produce butyl glycosides in high yields. Conversely to the case of water, n-butanol has only a slight effect on the recrystallization of ball-milled cellulose. As a result, thorough depolymerization of cellulose prior the glycosylation step is no longer required, which is a pivotal aspect with respect to energy consumption. This process was successfully transposed to wheat straw from which butyl glycosides and xylosides were produced in good yields. Butyl glycosides and xylosides are important chemicals as they can be used as hydrotropes but also as intermediates in the production of valuable amphiphilic alkyl glycosides.

Catalytic effect of aluminium chloride on the example of the conversion of sugar model compounds

Schwiderski, Martin,Kruse, Andrea

, p. 64 - 70 (2015/04/14)

Abstract In this work, the catalytic effect of the Bronsted acid hydrochloric acid, the Bronsted base sodium hydroxide and the Lewis acid AlCl3 on the conversion of biomass derived carbohydrates is investigated. On the example of the glycolaldehyde conversion, it is shown that the Lewis acid catalyses the ketol-endiol-tautomerism, the dehydration, the retro-aldol-reaction and the benzilic-acid-rearrangement. The main products are C4- and C6-carbohydrates as well as their secondary products 2-hydroxybut-3-enoic acid 1 and several furans. Under the same reaction conditions hydrochloric acid catalyzes mainly the dehydration and sodium hydroxide the tautomerism and subsequent aldolization.

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