Basic information
- Standard SMILES
NC(=O)c1ccc(O)cc1- InChIKey
QXSAKPUBHTZHKW-UHFFFAOYSA-N- Molecular formula
- C7H7NO2
- Average molar mass
- 137.14 g/mol
- Monoisotopic mass
- 137.04767846
Overview
P-Hydroxybenzamide is a member of benzamides.
Names & identifiers
- Preferred name
- 4-Hydroxybenzamide
- IUPAC
- 4-hydroxybenzamide
- English name
- 4-Hydroxybenzamide
- Molecular formula
- C7H7NO2
- Molecular weight
- 137.14
Names & synonyms
Show more names
Database identifiers
- CAS
619-57-8- PubChem CID
- 65052
- DTXSID
DTXSID10210931- ChEMBL
CHEMBL123617- ChEBI
CHEBI:220253- UNII
- 9OU5YD093J
- EC Number
- 210-602-7
- Nikkaji
- J94.905A
Properties
Computed structural properties
- XLogP
- 0.3
- Topological polar surface area
- 63.3 Ų
- Hydrogen bond donors
- 2
- Hydrogen bond acceptors
- 2
- Rotatable bonds
- 1
- Heavy atoms
- 10
- Formal charge
- 0
- Complexity
- 128
Experimental & physicochemical properties
Physicochemical properties
- Melting point
- 161 · 161-162 °C (lit.)
- Boiling point
- 345.3 · 345.3±25.0 °C(Predicted)
- Density
- 1.286 · 1.286±0.06 g/cm3(Predicted)
- storage temp.
- Sealed in dry,Room Temperature
- form
- powder to crystal
- pka
- 8.6 · 8.60±0.13(Predicted)
- color
- White to Light yellow to Dark green
- BRN
- 1906921 · 1906921
- InChI
- InChI=1S/C7H7NO2/c8-7(10)5-1-3-6(9)4-2-5/h1-4,9H,(H2,8,10)
- InChIKey
- QXSAKPUBHTZHKW-UHFFFAOYSA-N
- SMILES
- C(N)(=O)C1=CC=C(O)C=C1
- CAS DataBase Reference
- 619 · 619-57-8(CAS DataBase Reference)
- FDA UNII
- 9 OU5YD093J · 9OU5YD093J
- UNSPSC Code
- 12352100 · 12352100
- NACRES
- 22 · NA.22
- Symbol(GHS)
- 7 · GHS07
- Signal word
- Warning
- Hazard statements
- 315 · H315-H319-H335
- Precautionary statements
- 261 · P261-P264-P271-P280-P302+P352-P305+P351+P338
- target organs
- Respiratory system
- PPE
- 95 · dust mask type N95 (US), Eyeshields, Gloves
- Hazard Codes
- Xi
- Risk Statements
- 36 · 36/37/38
- Safety Statements
- 26 · 26-37/39-36
- WGK Germany
- 3 · 3
- HazardClass
- IRRITANT
- HS Code
- 29242990 · 29242990
- Storage Class
- 11 · 11 - Combustible Solids
- Hazard Classifications
- 2 Skin · Eye Irrit. 2Skin Irrit. 2STOT SE 3
Safety & regulation
GHS classification
GHS Classification
This chemical does not meet GHS hazard criteria for 11.3% (6 of 53) of reports.
Warning
H315 (88.7%): Causes skin irritation [Warning Skin corrosion/irritation]
P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, P319, P321, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 53 reports by companies from 8 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Hazard information
Safety data
- PPE
- dust mask type N95 (US), Eyeshields, Gloves
- wgk
- 3
- hs_code
- 29242990
- risk_code
- 36/37/38
- Signal word
- Warning
- Symbol(GHS)
- GHS07
- hazard_code
- Xi
- safety_code
- 26-37/39-36
- hazard_class
- IRRITANT
- Storage Class
- 11 - Combustible Solids
- target organs
- Respiratory system
- Hazard statements
- H315-H319-H335
- Hazard Classifications
- Eye Irrit. 2Skin Irrit. 2STOT SE 3
- Precautionary statements
- P261-P264-P271-P280-P302+P352-P305+P351+P338
Chemistry & industry
Applications
Uses4-Hydroxybenzamide is a secondary metabolite from marine sponge Phakellia fusca.
Uses4-Hydroxybenzamide was used in the synthesis of balanol, a potent protein kinase C (PKC) inhibitor.
General DescriptionThe standard molar enthalpy of formation of 4-hydroxybenzamide was studied by micro- or macrocombustion calorimetry.
Upstream & downstream products
Downstream products
Suppliers50 total
Additional notes
Definition4-Hydroxybenzamide (4HBM) is an important biological active compound that has the presence of various biological activities such as antimycobacterial, antifungal, antimicrobial, herbicidal, and antioxidant. The benzamide derivatives are also used in medical, pharmaceutical, and therapeutic applications because of their anti-inflammatory, antibacterial, and antifungal activities. The amine and carboxylic acids are important functional groups of present molecules. These are mainly utilized in the field of chemical industry. The cocrystallization of itraconazole (a very slightly soluble triazole antifungal drug) with 4-hydroxybenzamide (4OHBZA) can potentially increase the drug solubility at pH1.2 and 37 °C by 64 times[1-2].
Related reactions
Linked notes
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