Chemical Properties of Benzamide, 2-hydroxy-

InChI

InChI=1S/C7H7NO2/c8-7(10)5-3-1-2-4-6(5)9/h1-4,9H,(H2,8,10)

InChI Key

SKZKKFZAGNVIMN-UHFFFAOYSA-N

Formula

C7H7NO2

SMILES

NC(=O)c1ccccc1O

Molecular Weight¹

137.14

Other Names

• 2-Carbamoylphenol
• 2-Carboxamidophenol
• 2-hydroxybenzamide
• Acket
• Afko-Sal
• Algamon
• Algiamida
• Allevin
• Amid kyseliny salicylove
• Amid-Sal
• Amidosal
• Anamid
• Andasol
• Benesal
• Benzamide, o-hydroxy-
• Cetamide
• Cidal
• Cymidon
• Dolomide
• Dropsprin
• Eggosalil
• Flarpirina
• H.P. 34
• Liquiprin
• Morsarinas
• NSC 3115
• Novecyl
• OHB
• Oramid
• Panithal
• Raspberin
• SR 4326
• Salamid
• Salamide
• Saliamid
• Saliamin
• Salicilamide
• Salicim
• Salicylamid
• Salicylic Acid amide
• Salipur
• Salizell
• Salrin
• Salymid
• Samid
• Serramida
• Urtosal
• o-hydroxybenzamide
• salicylamide

• ω : Acentric Factor.
• Δ_cH°_solid : Standard solid enthalpy of combustion (kJ/mol).
• C_p,gas : Ideal gas heat capacity (J/mol×K).
• 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_fH°_solid : Solid phase enthalpy of formation at standard conditions (kJ/mol).
• Δ_fusH° : Enthalpy of fusion at standard conditions (kJ/mol).
• Δ_fusH : Enthalpy of fusion at a given temperature (kJ/mol).
• Δ_subH° : Enthalpy of sublimation at standard conditions (kJ/mol).
• Δ_vapH° : Enthalpy of vaporization at standard conditions (kJ/mol).
• Δ_vapH : Enthalpy of vaporization at a given temperature (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).
• I_np : Non-polar retention indices.
• 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	0.6758		Relay (1.0) Calculated Property
ΔcH°solid	-3352.40 ± 2.20	kJ/mol	NIST
ΔfG°	-96.62	kJ/mol	Joback Calculated Property
ΔfH°gas	-330.45	kJ/mol	Relay (1.0) Calculated Property
ΔfH°solid	-402.70 ± 2.20	kJ/mol	NIST
ΔfusH°	[27.40; 29.00]	kJ/mol
ΔfusH°	27.40	kJ/mol	Thermodynamic and structural aspects of hydroxybenzamide molecular crystals study
ΔfusH°	29.00	kJ/mol	Solubility and Melting Properties of Salicylamide
ΔsubH°	[99.30; 101.90]	kJ/mol
ΔsubH°	101.90 ± 0.40	kJ/mol	NIST
ΔsubH°	99.30 ± 1.30	kJ/mol	NIST
ΔvapH°	66.36	kJ/mol	Relay (1.0) Calculated Property
IE	8.58	eV	Relay (1.0) Calculated Property
log10WS	[-1.84; -1.78]
log10WS	-1.78		Aq. Solubility Prediction
log10WS	-1.84		Estimated Solubility
log10WS	-1.82		Estimated Solubility
logPoct/wat	0.491		Crippen Calculated Property
McVol	103.150	ml/mol	McGowan Calculated Property
Pc	6009.25	kPa	Joback Calculated Property
Inp	[1397.00; 1470.00]
Inp	1402.00		NIST
Inp	1397.00		NIST
Inp	1422.00		NIST
Inp	1450.00		NIST
Inp	1445.00		NIST
Inp	1450.00		NIST
Inp	1450.00		NIST
Inp	1460.00		NIST
Inp	1470.00		NIST
Inp	1450.00		NIST
Inp	1450.00		NIST
Inp	1405.00		NIST
Inp	1405.00		NIST
Inp	1435.00		NIST
Inp	1399.00		NIST
Inp	1409.00		NIST
Inp	1435.00		NIST
Inp	1435.00		NIST
Inp	1455.00		NIST
Inp	1405.00		NIST
Inp	1399.00		NIST
Tboil	543.50	K	Relay (1.0) Calculated Property
Tc	824.78	K	Relay (1.0) Calculated Property
Tfus	[413.95; 415.15]	K
Tfus	415.15	K	Jean-Claude Bradley Open Melting Point Dataset (2014, CC0) Compiled value
Tfus	413.95	K	Aq. Solubility Prediction
Tfus	414.00 ± 1.00	K	NIST
Vc	0.350	m3/kmol	Relay (1.0) Calculated Property

Temperature Dependent Properties

Property	Value	Unit	Temperature (K)	Source
Cp,solid	[124.10; 180.60]	J/mol×K	[280.40; 395.40]
Cp,solid	124.10	J/mol×K	280.40	Determination of the activity of a molecular solute in saturated solution
Cp,solid	126.30	J/mol×K	285.40	Determination of the activity of a molecular solute in saturated solution
Cp,solid	128.70	J/mol×K	290.40	Determination of the activity of a molecular solute in saturated solution
Cp,solid	130.90	J/mol×K	295.40	Determination of the activity of a molecular solute in saturated solution
Cp,solid	133.10	J/mol×K	300.40	Determination of the activity of a molecular solute in saturated solution
Cp,solid	135.60	J/mol×K	305.40	Determination of the activity of a molecular solute in saturated solution
Cp,solid	138.00	J/mol×K	310.40	Determination of the activity of a molecular solute in saturated solution
Cp,solid	140.50	J/mol×K	315.40	Determination of the activity of a molecular solute in saturated solution
Cp,solid	142.90	J/mol×K	320.40	Determination of the activity of a molecular solute in saturated solution
Cp,solid	145.50	J/mol×K	325.40	Determination of the activity of a molecular solute in saturated solution
Cp,solid	148.10	J/mol×K	330.40	Determination of the activity of a molecular solute in saturated solution
Cp,solid	150.50	J/mol×K	335.40	Determination of the activity of a molecular solute in saturated solution
Cp,solid	153.10	J/mol×K	340.40	Determination of the activity of a molecular solute in saturated solution
Cp,solid	155.60	J/mol×K	345.40	Determination of the activity of a molecular solute in saturated solution
Cp,solid	158.20	J/mol×K	350.40	Determination of the activity of a molecular solute in saturated solution
Cp,solid	160.60	J/mol×K	355.40	Determination of the activity of a molecular solute in saturated solution
Cp,solid	163.30	J/mol×K	360.40	Determination of the activity of a molecular solute in saturated solution
Cp,solid	165.60	J/mol×K	365.40	Determination of the activity of a molecular solute in saturated solution
Cp,solid	168.10	J/mol×K	370.40	Determination of the activity of a molecular solute in saturated solution
Cp,solid	170.30	J/mol×K	375.40	Determination of the activity of a molecular solute in saturated solution
Cp,solid	172.90	J/mol×K	380.40	Determination of the activity of a molecular solute in saturated solution
Cp,solid	175.40	J/mol×K	385.40	Determination of the activity of a molecular solute in saturated solution
Cp,solid	177.90	J/mol×K	390.40	Determination of the activity of a molecular solute in saturated solution
Cp,solid	180.60	J/mol×K	395.40	Determination of the activity of a molecular solute in saturated solution
ΔfusH	[27.10; 29.00]	kJ/mol	[411.90; 414.90]
ΔfusH	29.00	kJ/mol	411.90	NIST
ΔfusH	27.10	kJ/mol	414.90	NIST
ΔvapH	113.70	kJ/mol	298.15	Thermochemical studies on salicylaldehyde and salicylamide

Correlations

Property	Value	Unit	Temperature (K)	Source
Cp,gas	[134.91; 309.35]	J/mol×K	[273.00; 1000.00]	Joback Predicted correlation
Equation			Y = A + B·T + C·T² + D·T³ + E·T⁴ Y is Cp,gas in J/mol×K, T in K
Coefficient A			-3.24500e+01
Coefficient B			7.78400e-01
Coefficient C			-6.69260e-04
Coefficient D			2.32660e-07
Coefficient E			0.00000e+00
Temperature range, min.			273.00
Temperature range, max.			1000.00
Cp,gas	134.91	J/mol×K	273.00	Calculated Property
Cp,gas	169.47	J/mol×K	353.78	Calculated Property
Cp,gas	198.52	J/mol×K	434.56	Calculated Property
Cp,gas	222.79	J/mol×K	515.33	Calculated Property
Cp,gas	243.03	J/mol×K	596.11	Calculated Property
Cp,gas	259.96	J/mol×K	676.89	Calculated Property
Cp,gas	274.32	J/mol×K	757.67	Calculated Property
Cp,gas	286.85	J/mol×K	838.44	Calculated Property
Cp,gas	298.28	J/mol×K	919.22	Calculated Property
Cp,gas	309.35	J/mol×K	1000.00	Calculated Property

Similar Compounds

Find more compounds similar to Benzamide, 2-hydroxy-.

Mixtures

• Benzamide, 2-hydroxy- + 1-Octanol
• Benzamide, 2-hydroxy- + Dimethyl Sulfoxide
• Benzamide, 2-hydroxy- + Methyl Alcohol
• Benzamide, 2-hydroxy- + Acetonitrile
• Benzamide, 2-hydroxy- + Acetic acid
• Benzamide, 2-hydroxy- + Acetone
• Benzamide, 2-hydroxy- + Water
• Benzamide, 2-hydroxy- + Ethyl Acetate

Sources

• Jean-Claude Bradley Open Melting Point Dataset (2014, CC0) ChEDL chemicals 1.5.2, from Bradley, J.-C.; Williams, A.; Lang, A. Jean-Claude Bradley Open Melting Point Dataset. Figshare, 2014 (CC0).
• Cheméo Relay (1.0)
• Crippen Method
• Thermochemical studies on salicylaldehyde and salicylamide
• Determination of the activity of a molecular solute in saturated solution
• Partial molar volumes of some drug and pro-drug substances in 1-octanol at T = 298.15 K
• Effect of temperature on volumetric and viscometric properties of some non-steroidal anti-inflammatory drugs in aprotic solvents
• Thermodynamic and structural aspects of hydroxybenzamide molecular crystals study
• Solubility and Melting Properties of Salicylamide
• Volumetric and Viscometric Studies of Salicyl Amide, Salicylic Acid, and Acetyl Salicylic Acid in Alcohols at Different Temperatures
• Joback Method
• Aqueous Solubility Prediction Method
• Estimated Solubility Method
• McGowan Method
• NIST Webbook

Note: Cheméo is only indexing the data, follow the source links to retrieve the latest data. The source is also providing more information like the publication year, authors and more. Take the time to validate and double check the source of the data.
Calculated This icon marks a calculated value or equation: a prediction, not a measurement.
Compiled This icon marks a compiled value or equation: taken from a data compilation such as ChemSep, not from an original measurement report.
These property values are available through the Cheméo API. A free account gives you an access key.