Chemical Properties of Uridine (CAS 58-96-8)

InChI

InChI=1S/C9H12N2O6/c12-3-4-6(14)7(15)8(17-4)11-2-1-5(13)10-9(11)16/h1-2,4,6-8,12,14-15H,3H2,(H,10,13,16)/t4-,6-,7-,8-/m1/s1

InChI Key

DRTQHJPVMGBUCF-XVFCMESISA-N

Formula

C9H12N2O6

SMILES

O=c1ccn(C2OC(CO)C(O)C2O)c(=O)[nH]1

Molecular Weight¹

244.20

CAS

58-96-8

Other Names

• 1-((2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)pyrimidine-2,4(1H,3H)-dione
• 1-.beta.-D-ribofuranosyl-2,4(1H,3H)-pyrimidinedione
• 1-«beta»-D-Ribofuranosyl-2,4(1H,3H)-pyrimidinedione
• 1-«beta»-D-Ribofuranosyluracil
• NSC 20256
• Uracil riboside
• Uracil, 1-«beta»-D-ribofuranosyl-
• Uracil-1-«beta»-d-ribofuranoside
• Urd
• Uridin
• d-Ribosyl uracil
• «beta»-D-Ribofuranoside, 2,4(1H,3H)-pyrimidinedione-1
• «beta»-Uridine

• ω : Acentric Factor.
• PAff : Proton affinity (kJ/mol).
• BasG : Gas basicity (kJ/mol).
• C_p,solid : Solid phase heat capacity (J/mol×K).
• Δ_fG° : Standard Gibbs free energy of formation (kJ/mol).
• Δ_fH°_gas : Enthalpy of formation at standard conditions (kJ/mol).
• Δ_vapH° : Enthalpy of vaporization at standard conditions (kJ/mol).
• IE : Ionization energy (eV).
• log₁₀WS : Log10 of Water solubility in mol/l.
• logP_oct/wat : Octanol/Water partition coefficient.
• McVol : McGowan's characteristic volume (ml/mol).
• P_c : Critical Pressure (kPa).
• ρ_s : Solid Density (kg/m³).
• T_boil : Normal Boiling Point Temperature (K).
• T_c : Critical Temperature (K).
• T_fus : Normal melting (fusion) point (K).
• V_c : Critical Volume (m³/kmol).
• ¹: Molecular weight from the IUPAC atomic weights tables.

Physical Properties

Property	Value	Unit	Source
ω	0.9010		Relay (1.0) Calculated Property
PAff	[899.00; 947.60]	kJ/mol
PAff	947.60	kJ/mol	NIST
PAff	899.00	kJ/mol	NIST
BasG	916.60	kJ/mol	NIST
ΔfG°	-451.73	kJ/mol	Relay (1.0-beta) Calculated Property
ΔfH°gas	-857.63	kJ/mol	Relay (1.0) Calculated Property
ΔvapH°	163.53	kJ/mol	Relay (1.0) Calculated Property
IE	9.13	eV	Relay (1.0) Calculated Property
log10WS	-0.19		Relay (1.0) Calculated Property
logPoct/wat	-3.334		Crippen Calculated Property
McVol	158.230	ml/mol	McGowan Calculated Property
Pc	3307.82	kPa	Relay (1.0-beta) Calculated Property
Tboil	689.32	K	Relay (1.0) Calculated Property
Tc	986.44	K	Relay (1.0) Calculated Property
Tfus	448.15	K	Relay (1.0) Calculated Property
Vc	0.589	m3/kmol	Relay (1.0) Calculated Property

Temperature Dependent Properties

Property	Value	Unit	Temperature (K)	Source
Cp,solid	[292.34; 319.21]	J/mol×K	[298.15; 368.15]
Cp,solid	292.34	J/mol×K	298.15	Molar Heat Capacities of Some Derivatives of Uridine and 2'-Deoxyuridine
Cp,solid	294.26	J/mol×K	303.15	Molar Heat Capacities of Some Derivatives of Uridine and 2'-Deoxyuridine
Cp,solid	296.18	J/mol×K	308.15	Molar Heat Capacities of Some Derivatives of Uridine and 2'-Deoxyuridine
Cp,solid	298.10	J/mol×K	313.15	Molar Heat Capacities of Some Derivatives of Uridine and 2'-Deoxyuridine
Cp,solid	300.02	J/mol×K	318.15	Molar Heat Capacities of Some Derivatives of Uridine and 2'-Deoxyuridine
Cp,solid	301.93	J/mol×K	323.15	Molar Heat Capacities of Some Derivatives of Uridine and 2'-Deoxyuridine
Cp,solid	303.86	J/mol×K	328.15	Molar Heat Capacities of Some Derivatives of Uridine and 2'-Deoxyuridine
Cp,solid	305.77	J/mol×K	333.15	Molar Heat Capacities of Some Derivatives of Uridine and 2'-Deoxyuridine
Cp,solid	307.69	J/mol×K	338.15	Molar Heat Capacities of Some Derivatives of Uridine and 2'-Deoxyuridine
Cp,solid	309.61	J/mol×K	343.15	Molar Heat Capacities of Some Derivatives of Uridine and 2'-Deoxyuridine
Cp,solid	311.53	J/mol×K	348.15	Molar Heat Capacities of Some Derivatives of Uridine and 2'-Deoxyuridine
Cp,solid	313.45	J/mol×K	353.15	Molar Heat Capacities of Some Derivatives of Uridine and 2'-Deoxyuridine
Cp,solid	315.37	J/mol×K	358.15	Molar Heat Capacities of Some Derivatives of Uridine and 2'-Deoxyuridine
Cp,solid	317.29	J/mol×K	363.15	Molar Heat Capacities of Some Derivatives of Uridine and 2'-Deoxyuridine
Cp,solid	319.21	J/mol×K	368.15	Molar Heat Capacities of Some Derivatives of Uridine and 2'-Deoxyuridine
ρs	1600.00	kg/m3	298.15	Saturation molalities and standard molar enthalpies of solution of cytidine(cr), hypoxanthine(cr), thymidine(cr), thymine(cr), uridine(cr), and xanthine(cr) in H2O(l)

Similar Compounds

Find more compounds similar to Uridine.

Mixtures

• Uridine + Water

Sources

• Cheméo Relay (1.0)
• Cheméo Relay (1.0, beta) Beta: served but experimental, data-limited and below our cross-validation release bar; the Joback value is recommended where available.
• Crippen Method
• Crippen Method
• Saturation molalities and standard molar enthalpies of solution of cytidine(cr), hypoxanthine(cr), thymidine(cr), thymine(cr), uridine(cr), and xanthine(cr) in H2O(l)
• The partial molar volumes at T = (288.15 to 313.15) K, and the partial molar heat capacities and expansions at T = 298.15 K of cytidine, uridine, and adenosine in aqueous solution
• Volumetric interaction coefficients for some nucleosides in aqueous solution at T= 298.15 K
• Volumetric properties of the nucleosides adenosine, cytidine, and uridine in aqueous solution at T=298.15K and P=(10 to120)MPa
• Volumetric studies on nucleic acid bases and nucleosides in aqueous guanidine hydrochloride solutions at T = (288.15 to 318.15) K and at atmospheric pressure
• Solvation behavior of some nucleic acid bases and nucleosides in water and in aqueous guanidine hydrochloride solutions: Viscometric, calorimetric and spectroscopic approach
• Energetic characterization of a bioactive compound: Uridine
• Partial Molar Isentropic and Isothermal Compressions of the Nucleosides Adenosine, Cytidine, and Uridine in Aqueous Solution at 298.15 K
• Molar Heat Capacities of Some Derivatives of Uridine and 2'-Deoxyuridine
• McGowan Method
• NIST Webbook

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