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2'-Deoxycytidine hydrochloride

CAS# 3992-42-5

2'-Deoxycytidine hydrochloride

Catalog No. BCC5434----Order now to get a substantial discount!

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Chemical structure

2'-Deoxycytidine hydrochloride

3D structure

Chemical Properties of 2'-Deoxycytidine hydrochloride

Cas No. 3992-42-5 SDF Download SDF
PubChem ID 107488 Appearance Powder
Formula C9H14ClN3O4 M.Wt 263.68
Type of Compound N/A Storage Desiccate at -20°C
Synonyms 2'-Deoxycytidine monohydrochloride; Deoxycytidine hydrochloride; NSC 83251
Solubility H2O : ≥ 41 mg/mL (155.49 mM)
*"≥" means soluble, but saturation unknown.
Chemical Name 4-amino-1-[(2R,4S,5R)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]pyrimidin-2-one;hydrochloride
SMILES C1C(C(OC1N2C=CC(=NC2=O)N)CO)O.Cl
Standard InChIKey LTKCXZGFJFAPLY-OERIEOFYSA-N
Standard InChI InChI=1S/C9H13N3O4.ClH/c10-7-1-2-12(9(15)11-7)8-3-5(14)6(4-13)16-8;/h1-2,5-6,8,13-14H,3-4H2,(H2,10,11,15);1H/t5-,6+,8+;/m0./s1
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.

2'-Deoxycytidine hydrochloride Dilution Calculator

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2'-Deoxycytidine hydrochloride Molarity Calculator

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Preparing Stock Solutions of 2'-Deoxycytidine hydrochloride

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 3.7925 mL 18.9624 mL 37.9248 mL 75.8495 mL 94.8119 mL
5 mM 0.7585 mL 3.7925 mL 7.585 mL 15.1699 mL 18.9624 mL
10 mM 0.3792 mL 1.8962 mL 3.7925 mL 7.585 mL 9.4812 mL
50 mM 0.0758 mL 0.3792 mL 0.7585 mL 1.517 mL 1.8962 mL
100 mM 0.0379 mL 0.1896 mL 0.3792 mL 0.7585 mL 0.9481 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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Background on 2'-Deoxycytidine hydrochloride

Deoxyguanosine Hcl(2'-Deoxyguanosine Hcl) is composed of the purine nucleoside guanine linked by its N9 nitrogen to the C1 carbon of deoxyribose.

References:
[1]. Deoxyguanosine, From Wikipedia

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References on 2'-Deoxycytidine hydrochloride

Free radical formation in X-irradiated crystals of 2'-deoxycytidine hydrochloride. Electron magnetic resonance studies at 10 K.[Pubmed:10825758]

Radiat Res. 2000 Jun;153(6):823-34.

Single crystals of deoxycytidine hydrochloride (CdR.HCl) have been X-irradiated at 10 K with doses up to about 150 kGy and studied using 24 GHz (K-band) EPR, ENDOR and FSE spectroscopy. In this system, the cytosine base is protonated at the N3 position. Nine different radicals were characterized and identified. Three of these are ascribed to three versions of the one-electron reduced species, probably differing in their protonation state. Radicals formed by net hydrogen addition to the cytosine C5 and C6 positions were observed at 10 K. The hydrogen-abstraction radical at the deoxyribose C1' position most probably results from initial oxidation of the base. The remaining radical species are all localized to the sugar moiety, representing products formed by net hydrogen abstraction from three of the five available carbons of the deoxyribose sugar. The lack of base-centered oxidation products as well as the structures of the one-electron reduced species is rationalized by considering the specific proton donor-acceptor properties of this crystalline lattice in comparison with similar systems.

Description

2'-Deoxycytidine hydrochloride is composed of the purine nucleoside guanine linked by its N9 nitrogen to the C1 carbon of deoxyribose.

Keywords:

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