P21005
4-Phenylbutyric acid
99%
Synonyme(s) :
γ-Phenylbutanoic acid, ψ-Phenylbutanoic acid, 4-Phenyl-n-butyric acid, 4-Phenylbutanoic acid, Benzenebutyric acid
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A propos de cet article
Formule linéaire :
C6H5(CH2)3COOH
Numéro CAS:
Poids moléculaire :
164.20
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
217-341-8
Beilstein/REAXYS Number:
638180
MDL number:
Assay:
99%
Form:
crystals
Service technique
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Laissez-nous vous aiderQuality Level
assay
99%
form
crystals
bp
165 °C/10 mmHg (lit.)
mp
49-51 °C (lit.)
SMILES string
OC(=O)CCCc1ccccc1
InChI
1S/C10H12O2/c11-10(12)8-4-7-9-5-2-1-3-6-9/h1-3,5-6H,4,7-8H2,(H,11,12)
InChI key
OBKXEAXTFZPCHS-UHFFFAOYSA-N
General description
4-Phenylbutyric acid (4-PBA) is used in the treatment of urea cycle disorders.
Application
4-PBA has been used as a selective inhibitor of endoplasmic reticulum stress (ERS).
It can also be used as a reactant in the synthesis of:
It can also be used as a reactant in the synthesis of:
- 1-Tetralone using Lewis acid catalyst.
- 4,N-diphenylbutyramide.
Classe de stockage
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Clean, reusable and low cost heterogeneous catalyst for amide synthesis
Comerford JW, et al.
Chemical Communications (Cambridge, England), 18(21), 2562-2564 (2009)
Synthesis of 1-tetralones by intramolecular Friedel?Crafts reaction of 4-arylbutyric acids using Lewis acid catalysts
Cui DM, et al.
Tetrahedron Letters, 44(21), 4007-4010 (2003)
Induction of apoptosis coupled to endoplasmic reticulum stress through regulation of CHOP and JNK in bone marrow mesenchymal stem cells from patients with systemic lupus erythematosus
Guo G, et al.
Journal of immunology research (2015)