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Tagatose is a naturally occurring monosaccharide, similar in chemical structure to fructose. It is a low-calorie sweetener with a taste and sweetness comparable to common table sugar. However, it is absorbed more slowly in the body, making it a potentially viable alternative for those managing calorie consumption or blood sugar levels. Tagatose is found naturally in small amounts in some dairy products and can be commercially produced through the enzymatic hydrolysis of lactose. It is generally recognized as safe (GRAS) by the U.S. Food and Drug Administration.

17598-81-1

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17598-81-1 Usage

Uses

Used in Food Industry:
Tagatose is used as a low-calorie sweetener for its reduced caloric value compared to other sugars, making it suitable for consumers looking to manage their calorie intake or blood sugar levels.
Used in Pharmaceutical Industry:
Tagatose is used as a potential alternative for managing blood sugar levels, particularly for individuals with diabetes or those at risk of developing the condition, due to its slower absorption rate in the body.
Used in Dairy Products:
Tagatose is used as a natural sweetener in dairy products, where it is found in small amounts, to enhance the taste without significantly increasing the caloric content.

Check Digit Verification of cas no

The CAS Registry Mumber 17598-81-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,5,9 and 8 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 17598-81:
(7*1)+(6*7)+(5*5)+(4*9)+(3*8)+(2*8)+(1*1)=151
151 % 10 = 1
So 17598-81-1 is a valid CAS Registry Number.
InChI:InChI=1/C6H12O6/c7-1-3(9)5(11)6(12)4(10)2-8/h3,5-9,11-12H,1-2H2/t3-,5+,6-/m1/s1

17598-81-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name Fructose

1.2 Other means of identification

Product number -
Other names DL-Fructose

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:17598-81-1 SDS

17598-81-1Relevant articles and documents

Hydroxyapatite-Supported Polyoxometalates for the Highly Selective Aerobic Oxidation of 5-Hydroxymethylfurfural or Glucose to 2,5-Diformylfuran under Atmospheric Pressure

Guan, Hongyu,Li, Ying,Wang, Qiwen,Wang, Xiaohong,Yu, Hang

, p. 997 - 1005 (2021/08/06)

(NH4)5H6PV8Mo4O40 supported on hydroxyapatite (HAP) (PMo4V8/HAP (n)) was prepared through the ion exchange of hydroxy groups. This ion exchange favored the oxidative conversion of 5-hydroxymethylfurfural (5-HMF) to 2,5-diformylfuran (DFF) in a one-pot cascade reaction with 96.0 % conversion and 83.8 % yield under 10 mL/min of O2 flow. PMo4V8/HAP (31) was used to explore the production of DFF directly from glucose with the highest yield of 47.9 % so far under atmospheric oxygen, whereas the yield of DFF increased to 54.7 % in a one-pot and two-step reaction. These results indicated that the active sites in PMo4V8/HAP (31) retained their activities without any interference toward one another, which enabled the production of DFF in a more cost-saving way by only using oxygen and one catalyst in a one-step reaction. Meanwhile, the rigid structure of HAP and strong interaction in PMo4V8/HAP (31) allowed this catalyst to be reused for at least six times with high stability and duration.

Few-Unit-Cell MFI Zeolite Synthesized using a Simple Di-quaternary Ammonium Structure-Directing Agent

Abeykoon, Milinda,Al-Thabaiti, Shaeel,Bell, Alexis T.,Boscoboinik, J. Anibal,Dai, Heng,Dauenhauer, Paul,Dorneles de Mello, Matheus,Duan, Xuekui,Ghosh, Supriya,Kamaluddin, Huda Sharbini,Khan, Zaheer,Kumar, Gaurav,Li, Xinyu,Lu, Peng,Luo, Tianyi,Mkhoyan, K. Andre,Narasimharao, Katabathini,Qi, Liang,Rimer, Jeffrey D.,Tsapatsis, Michael

supporting information, p. 19214 - 19221 (2021/08/09)

Synthesis of a pentasil-type zeolite with ultra-small few-unit-cell crystalline domains, which we call FDP (few-unit-cell crystalline domain pentasil), is reported. FDP is made using bis-1,5(tributyl ammonium) pentamethylene cations as structure directing agent (SDA). This di-quaternary ammonium SDA combines butyl ammonium, in place of the one commonly used for MFI synthesis, propyl ammonium, and a five-carbon nitrogen-connecting chain, in place of the six-carbon connecting chain SDAs that are known to fit well within the MFI pores. X-ray diffraction analysis and electron microscopy imaging of FDP indicate ca. 10 nm crystalline domains organized in hierarchical micro-/meso-porous aggregates exhibiting mesoscopic order with an aggregate particle size up to ca. 5 μm. Al and Sn can be incorporated into the FDP zeolite framework to produce active and selective methanol-to-hydrocarbon and glucose isomerization catalysts, respectively.

Method for preparing lactic acid through catalytically converting carbohydrate

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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.

Method for preparing fructose (by machine translation)

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Paragraph 0070-0101, (2020/07/02)

The method comprises the following steps: (1) reacting glucose with a catalyst in the presence of alcohol and carrying out reaction to obtain fructose-containing product; wherein the weight ratio of the glucose to the mixture of the titanium silicalite molecular sieve and the tin-silicon molecular sieve 50 - 600 is below 30 °C: (100 °C 0.1 - 6 1 1 - 10h) The method disclosed by the invention has high glucose conversion rate and fructose yield. (by machine translation)

Bi-Functional Magnesium Silicate Catalyzed Glucose and Furfural Transformations to Renewable Chemicals

Kumar, Abhinav,Srivastava, Rajendra

, p. 4807 - 4816 (2020/08/24)

Bio-refinery is attracting significant interest to produce a wide range of renewable chemicals and fuels from biomass that are alternative to fossil fuel derived petrochemicals. Similar to petrochemical industries, bio-refinery also depends on solid zeolite catalysts. Acid-base catalysis plays pivotal role in producing a wide range of chemicals from biomass. Herein, the Mg framework substituted MTW zeolite is synthesized and explored in the valorisation of glucose and furfural. Bi-functional (acidic and basic) characteristics are confirmed using pyridine adsorbed FT?IR analysis and NH3 and CO2 temperature-programmed desorption techniques. Textural properties and morphological information are retrieved from N2-sorption, X-ray photoelectron spectroscopy, and electron microscopy. The activity of the catalyst is demonstrated in the selective isomerisation of glucose to fructose in ethanol. Glucose is converted to methyl lactate in high yield using the same catalyst. Further, the bi-functional activity of this catalyst is demonstrated in the production of fuel precursor by the reaction of furfural and isopropanol. Mg?MTW zeolite exhibits excellent activity in the production of all these chemicals and fuel derivative. The catalyst exhibits no significant loss in the activity even after five recycles. One simple catalyst affording three renewable synthetic intermediates from glucose and furfural will attract significant attention to catalysis researchers and industrialists.

PROCESSES FOR PREPARING SORBOSE FROM GLUCOSE

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Paragraph 0012-0013; 0016-0018; 0035-0037; 0038, (2020/08/25)

Processes for converting glucose to sorbose with tailored selectivity. The processes include contacting glucose with a silica-containing structure that includes a zeolite having a topology of a 10-membered ring or smaller and Lewis acidic M4+ framework centers, wherein M is Ti, Sn, Zr, or Hf. Contacting the glucose is conducted under reaction conditions sufficient to isomerize the glucose to sorbose.

Role of the Strong Lewis Base Sites on Glucose Hydrogenolysis

Yazdani, Parviz,Wang, Bo,Gao, Feng,Kawi, Sibudjing,Borgna, Armando

, p. 3845 - 3853 (2018/07/31)

This work reports the individual role of strong Lewis base sites on catalytic conversion of glucose hydrogenolysis to acetol/lactic acid, including glucose isomerisation to fructose and pyruvaldehyde rearrangement/hydrogenation to acetol/lactic acid. Las

A catalyzed by a chemical method, a method of glucose isomerization to fructose

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Paragraph 0043; 0044, (2017/02/28)

The invention discloses a chemical method for catalyzing glucose into fructose through isomerization, and relates to fructose. The method comprises the following steps: mixing a water solution containing Mg(NO3)2.6H2O, Al(NO3)3.6H2O, and Zr(NO3)4.5H2O/Sn(NO3).6H2O/Cu(NO3)2.3H2O with a NaOH water solution and a Na2CO3 water solution, wherein the metal molar mass ratio of Mg:Al:M is equal to 3:1:1, M represents Zr, Sn, or Cu, pH is 8 to 8, and the temperature is 60 DEG C; carrying out aging on the precipitate in the mother liquid, then carrying out static crystallization, drying so as to obtain the trinary metal hydrotalcite, adding the trinary metal hydrotalcite into a glucose solution to carry out reactions, filtering so as to obtain isomerized glucose solution and a solid hydrotalcite catalyst, recycling the catalyst, and finally subjecting the filtrate to vacuum rotation evaporation so as to obtain a condensed fructose liquid, wherein the weight ratio of the trinary metal hydrotalcite to the glucose to solvent (water) is (1-4):(1-10):40.

Characterization of glycerol phosphate oxidase from Streptococcus pneumoniae and its application for ketose synthesis

Li, Zijie,Qiao, Yingxin,Cai, Li,Nakanishi, Hideki,Gao, Xiao-Dong

supporting information, p. 504 - 507 (2015/03/05)

Glycerol phosphate oxidase from Streptococcus pneumoniae (GPOS.pne) was purified and characterized. By the actions of GPOS.pne and dihydroxyacetone phosphate (DHAP)-dependent aldolases, various ketoses including rare sugars were synthesized with glyceraldehydes as acceptors in a one-pot four-enzyme system.

Facile enzymatic synthesis of ketoses

Wen, Liuqing,Huang, Kenneth,Wei, Mohui,Meisner, Jeffrey,Liu, Yunpeng,Garner, Kristina,Zang, Lanlan,Wang, Xuan,Li, Xu,Fang, Junqiang,Zhang, Houcheng,Wang, Peng George

supporting information, p. 12654 - 12658 (2015/10/28)

Studies of rare ketoses have been hampered by a lack of efficient preparation methods. A convenient, efficient, and cost-effective platform for the facile synthesis of ketoses is described. This method enables the preparation of difficult-to-access ketopentoses and ketohexoses from common and inexpensive starting materials with high yield and purity and without the need for a tedious isomer separation step. A spoonful of sugar: A convenient, efficient, and cost-effective platform for the facile synthesis of ketoses is described. This method, which involves a one-pot mulitenzyme (OPME) reaction, enables the preparation of rare ketopentoses and ketohexoses from common and inexpensive starting materials with high yield and purity and without the need for a tedious isomer separation step.

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