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3615-56-3

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3615-56-3 Usage

Chemical Properties

white fine crystalline powder

Definition

ChEBI: The D-stereoisomer of sorbopyranose.

Check Digit Verification of cas no

The CAS Registry Mumber 3615-56-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,1 and 5 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3615-56:
(6*3)+(5*6)+(4*1)+(3*5)+(2*5)+(1*6)=83
83 % 10 = 3
So 3615-56-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H12O6/c7-2-6(11)5(10)4(9)3(8)1-12-6/h3-5,7-11H,1-2H2/t3-,4+,5-,6+/m1/s1

3615-56-3 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (B21208)  D-Sorbose, 98%   

  • 3615-56-3

  • 0.1g

  • 910.0CNY

  • Detail
  • Alfa Aesar

  • (B21208)  D-Sorbose, 98%   

  • 3615-56-3

  • 0.5g

  • 3905.0CNY

  • Detail
  • Sigma

  • (S4887)  D-(+)-Sorbose  ≥99%

  • 3615-56-3

  • S4887-100MG

  • 1,344.33CNY

  • Detail

3615-56-3SDS

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 D-sorbopyranose

1.2 Other means of identification

Product number -
Other names D-Sorbose

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:3615-56-3 SDS

3615-56-3Relevant articles and documents

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 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)

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.

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