Welcome to LookChem.com Sign In|Join Free

CAS

  • or

3615-56-3

Post Buying Request

3615-56-3 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

3615-56-3 Usage

Description

D-(+)-Sorbose, also known as the D-stereoisomer of sorbopyranose, is a white fine crystalline powder with unique chemical properties. It is a naturally occurring sugar alcohol that plays a significant role in various industrial applications due to its distinctive characteristics.

Uses

Used in Pharmaceutical Industry:
D-(+)-Sorbose is used as an intermediate in the synthesis of various pharmaceutical compounds for its ability to serve as a building block in the production of drugs. Its unique stereochemistry allows it to be a key component in the development of new medications.
Used in Food and Beverage Industry:
D-(+)-Sorbose is used as a sweetener and flavor enhancer for its natural sugar-like taste and ability to improve the taste profile of food and beverages. Its low caloric content and reduced impact on blood sugar levels make it a preferred choice for health-conscious consumers.
Used in Cosmetics Industry:
D-(+)-Sorbose is used as a humectant and moisturizing agent in cosmetic products for its ability to retain moisture and improve skin hydration. Its gentle and non-irritating properties make it suitable for use in skincare formulations.
Used in Biotechnology:
D-(+)-Sorbose is used in biotechnological applications for its role in the production of biofuels and other bio-based materials. Its potential as a renewable resource and its ability to be fermented make it a valuable component in the development of sustainable technologies.
Used in Research and Development:
D-(+)-Sorbose is used as a research compound for studying the properties and applications of sugar alcohols and their derivatives. Its unique stereochemistry provides valuable insights into the behavior of chiral molecules and their interactions with biological systems.

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 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.

PROCESSES FOR PREPARING SORBOSE FROM GLUCOSE

-

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.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 3615-56-3