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13360-52-6

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13360-52-6 Usage

General Description

Beta-cellobiose is a disaccharide composed of two glucose molecules linked together by a beta-1,4-glycosidic bond. It is a form of cellobiose, which is a common sugar found in cellulose, the main structural component of plant cell walls. Beta-cellobiose is produced through the enzymatic hydrolysis of cellulose, and it is often used in research and industrial applications as a substrate for cellulase enzymes. These enzymes break down beta-cellobiose into individual glucose molecules, which can then be utilized in various processes, such as biofuel production and the manufacturing of pharmaceuticals and food products. Additionally, beta-cellobiose has potential applications in the development of biodegradable materials and as a dietary supplement for its prebiotic effects in promoting the growth of beneficial gut bacteria.

Check Digit Verification of cas no

The CAS Registry Mumber 13360-52-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,3,6 and 0 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 13360-52:
(7*1)+(6*3)+(5*3)+(4*6)+(3*0)+(2*5)+(1*2)=76
76 % 10 = 6
So 13360-52-6 is a valid CAS Registry Number.

13360-52-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name .β.-Cellobiose

1.2 Other means of identification

Product number -
Other names β-D-Glucopyranose, 4-O-β-D-glucopyranosyl-

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:13360-52-6 SDS

13360-52-6Relevant articles and documents

CHARACTERIZATION OF MONO- AND OLIGOSACCHARIDES PRODUCED BY CO2 LASER IRRADIATION ON CELLULOSE

Suzuki, Jun,Azuma, Jun-ichi,Koshijima, Tetsuo,Okamura, Keizo,Okamoto, Hajime

, p. 481 - 484 (1983)

The chemical structures of three mono-, two di-, and two trisaccharides (1 - 7) isolated from the pyrolysis products formed by CO2 laser irradiation on cellulose were investigated.

Biochemical characterization and low-resolution SAXS structure of two-domain endoglucanase BlCel9 from Bacillus licheniformis

de Araújo, Evandro Ares,de Oliveira Neto, Mário,Polikarpov, Igor

, p. 1275 - 1287 (2019)

Lignocellulose feedstock constitutes the most abundant carbon source in the biosphere; however, its recalcitrance remains a challenge for microbial conversion into biofuel and bioproducts. Bacillus licheniformis is a microbial mesophilic bacterium capable of secreting a large number of glycoside hydrolase (GH) enzymes, including a glycoside hydrolase from GH family 9 (BlCel9). Here, we conducted biochemical and biophysical studies of recombinant BlCel9, and its low-resolution molecular shape was retrieved from small angle X-ray scattering (SAXS) data. BlCel9 is an endoglucanase exhibiting maximum catalytic efficiency at pH?7.0 and 60?°C. Furthermore, it retains 80% of catalytic activity within a broad range of pH values (5.5–8.5) and temperatures (up to 50?°C) for extended periods of time (over 48?h). It exhibits the highest hydrolytic activity against phosphoric acid swollen cellulose (PASC), followed by bacterial cellulose (BC), filter paper (FP), and to a lesser extent carboxymethylcellulose (CMC). The HPAEC-PAD analysis of the hydrolytic products demonstrated that the end product of the enzymatic hydrolysis is primarily cellobiose, and also small amounts of glucose, cellotriose, and cellotetraose are produced. SAXS data analysis revealed that the enzyme adopts a monomeric state in solution and has a molecular mass of 65.8?kDa as estimated from SAXS data. The BlCel9 has an elongated shape composed of an N-terminal family 3 carbohydrate-binding module (CBM3c) and a C-terminal GH9 catalytic domain joined together by 20 amino acid residue long linker peptides. The domains are closely juxtaposed in an extended conformation and form a relatively rigid structure in solution, indicating that the interactions between the CBM3c and GH9 catalytic domains might play a key role in cooperative cellulose biomass recognition and hydrolysis.

Ionic liquid tolerant hyperthermophilic cellulases for biomass pretreatment and hydrolysis

Datta, Supratim,Holmes, Bradley,Park, Joshua I.,Chen, Zhiwei,Dibble, Dean C.,Hadi, Masood,Blanch, Harvey W.,Simmons, Blake A.,Sapra, Rajat

, p. 338 - 345 (2010)

One of the main barriers to the enzymatic hydrolysis of cellulose results from its highly crystalline structure. Pretreating biomass with ionic liquids (IL) increases enzyme accessibility and cellulose recovery through precipitation with an anti-solvent. For an industrially feasible pretreatment and hydrolysis process, it is necessary to develop cellulases that are stable and active in the presence of small amounts of ILs co-precipitated with recovered cellulose. However, a significant decrease in cellulase activity in the presence of trace amounts of ILs has been reported in the literature, necessitating extensive processing to remove residual ILs from the regenerated cellulose. Towards that end, we have investigated the stability of hyperthermophilic enzymes in the presence of the IL 1-ethyl-3-methylimidazolium acetate ([C2mim][OAc]) and compared it to the industrial benchmark Trichoderma viride (T. viride) cellulase. The endoglucanase from a hyperthermophilic bacterium, Thermatoga maritima, and a hyperthermophilic archaeon, Pyrococcus horikoshii, were over expressed in E. coli and purified to homogeneity. Under their optimum conditions, both hyperthermophilic enzymes showed significantly higher [C2mim][OAc] tolerance than T. viride cellulase. Using differential scanning calorimetry we determined the effect of [C2mim][OAc] on protein stability and our data indicates that higher concentrations of IL correlated with lowered protein stability. Both hyperthermophilic enzymes were active on [C2mim][OAc] pretreated Avicel and corn stover. Furthermore, these enzymes can be recovered with little loss in activity after exposure to 15% [C2mim][OAc] for 15 h. These results demonstrate the potential of using IL-tolerant extremophilic cellulases for hydrolysis of IL-pretreated lignocellulosic biomass, for biofuel production.

Hydrolysis behaviors of sugarcane bagasse pith in subcritical carbon dioxide-water

Liang, Jiezhen,Chen, Xiaopeng,Wang, Linlin,Wei, Xiaojie,Qiu, Feifei,Lu, Chaochao

, p. 99322 - 99330 (2016/11/02)

The aim of this study was to describe the hydrolysis behavior of sugarcane bagasse pith (SCBP) in subcritical CO2-water. The hydrolysis was carried out in a batch reactor using different temperatures (160 to 260 °C), liquid to solid ratios (20:1 to 100:1), CO2 pressures (0 to 7.3 MPa), stirring speeds (0 to 500 rpm) and reaction times (0 to 40 min). The highest total reducing sugar yield (43.6%) was obtained at 200 °C, liquid to solid ratio 30:1, 2 MPa CO2, 500 rpm and 50 min. Two-dimensional heteronuclear single quantum coherence (2D HSQC) nuclear magnetic resonance (NMR), scanning electron microscopy (SEM) and Fourier transform infrared spectrometry (FT-IR) were used to help elucidate the physical and chemical characteristics of the raw material and residual solid particles, with results consistent with the removal of hemicellulose during hydrolysis. The changes in the concentration of products with time were analyzed to understand product distribution through high-performance liquid chromatography (HPLC) and to infer the reaction mechanism.

Optimization and hydrolysis of cellulose under subcritical water treatment for the production of total reducing sugars

Mohan, Mood,Timung, Robinson,Deshavath, Narendra Naik,Banerjee, Tamal,Goud, Vaibhav V.,Dasu, Venkata V.

, p. 103265 - 103275 (2015/12/23)

Subcritical water (SCW) treatment has gained enormous attention as an environmentally friendly technique for organic matter and an attractive reaction medium for a variety of applications. In this work, hydrolysis of cellulose was studied under SCW conditions in a batch reactor to attain total reducing sugars (TRS) within a reaction temperature and time range of 150 to 250 °C and 10-60 min, respectively. From the experimental results, the highest yield of TRS was 45.04% as obtained at 200 °C and 20 min of hydrolysis time. The characterisation techniques, namely X-ray diffraction (XRD) and Fourier transform infrared (FTIR) spectroscopy were used as to determine the structural and compositional changes in the hydrolysed material. Reaction parameters such as temperature, time, and solute loading have been optimised using response surface methodology based on a central composite design. From ANOVA analysis, it was described that the second-order response surface model is highly significant as per Fisher's F-test and P-value. A first-order reaction kinetic model was formulated to describe the hydrolysis of cellulose for TRS formation and decomposition. For TRS formation, the activation energy and pre-exponential factor of the Arrhenius equation was found to be 29.16 kJ mol-1 and 0.088 min-1 for 60 min, respectively.

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