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Chitotriose Trihydrochloride

CAS# 117436-78-9

Chitotriose Trihydrochloride

2D Structure

Catalog No. BCX1421----Order now to get a substantial discount!

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Chitotriose Trihydrochloride: 5mg Please Inquire In Stock
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Quality Control of Chitotriose Trihydrochloride

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Chitotriose Trihydrochloride

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Chemical Properties of Chitotriose Trihydrochloride

Cas No. 117436-78-9 SDF Download SDF
PubChem ID N/A Appearance Powder
Formula C18H38Cl3N3O13 M.Wt 610.86
Type of Compound N/A Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
General tips For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.Stock solution can be stored below -20℃ for several months.
We recommend that you prepare and use the solution on the same day. However, if the test schedule requires, the stock solutions can be prepared in advance, and the stock solution must be sealed and stored below -20℃. In general, the stock solution can be kept for several months.
Before use, we recommend that you leave the vial at room temperature for at least an hour before opening it.
About Packaging 1. The packaging of the product may be reversed during transportation, cause the high purity compounds to adhere to the neck or cap of the vial.Take the vail out of its packaging and shake gently until the compounds fall to the bottom of the vial.
2. For liquid products, please centrifuge at 500xg to gather the liquid to the bottom of the vial.
3. Try to avoid loss or contamination during the experiment.
Shipping Condition Packaging according to customer requirements(5mg, 10mg, 20mg and more). Ship via FedEx, DHL, UPS, EMS or other couriers with RT, or blue ice upon request.

Source of Chitotriose Trihydrochloride

Shrimp and crab shell

Chitotriose Trihydrochloride Dilution Calculator

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Chitotriose Trihydrochloride Molarity Calculator

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Preparing Stock Solutions of Chitotriose Trihydrochloride

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 1.637 mL 8.1852 mL 16.3704 mL 32.7407 mL 40.9259 mL
5 mM 0.3274 mL 1.637 mL 3.2741 mL 6.5481 mL 8.1852 mL
10 mM 0.1637 mL 0.8185 mL 1.637 mL 3.2741 mL 4.0926 mL
50 mM 0.0327 mL 0.1637 mL 0.3274 mL 0.6548 mL 0.8185 mL
100 mM 0.0164 mL 0.0819 mL 0.1637 mL 0.3274 mL 0.4093 mL
* Note: If you are in the process of experiment, it's necessary to make the dilution ratios of the samples. The dilution data above is only for reference. Normally, it's can get a better solubility within lower of Concentrations.

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References on Chitotriose Trihydrochloride

A novel method for chemo-enzymatic synthesis of elicitor-active chitosan oligomers and partially N-deacetylated chitin oligomers using N-acylated chitotrioses as substrates in a lysozyme-catalyzed transglycosylation reaction system.[Pubmed:8593620]

Carbohydr Res. 1995 Dec 27;279:151-60.

N,N',N"-Tri(monochloro)acetylchitotriose prepared by N-monochloroacetylation of Chitotriose Trihydrochloride was successfully polymerized into higher-molecular-weight oligomers by a lysozyme-catalyzed transglycosylation reaction, and a following base-catalyzed N-demonochloroacetylation gave a chitosan oligomer mixture mainly composed of oligomers with dp > 6. Partially N-deacetylated chitin oligomers (DAC oligomers) with dp 4-12 were synthesized by the enzyme reaction using N,N',N"-tri(monochloro)acetylchitotriose and N,N',N"-triacetylchitotriose (chitin trimer) as initial substrates followed by N-demonochloroacetylation. The structures of synthetic oligomers were analyzed by 1H NMR spectroscopy, enzymatic hydrolysis and nitrous acid deamination-NaBH4 reduction treatment. The dp of synthetic oligomers was measured by MALDI TOF MS (matrix-assisted laser desorption ionization time-of-flight mass spectrometry) using per-N-acetylated derivatives. The synthetic chitosan and DAC oligomers were strong elicitors for phytoalexin induction in Pisum sativum and Phaseolus vulgaris. This chemo-enzymatic method utilizing N-acylated chitotrioses as substrates is a novel approach to the synthesis of high-molecular-weight chitosan oligomers and DAC oligomers of biological importance.

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