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Merck
CN

262412

4-(Butylamino)benzoic acid

97%, for peptide synthesis

Synonym(s):

p-Butylaminobenzoic acid

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About This Item

Linear Formula:
CH3(CH2)3NHC6H4CO2H
CAS Number:
4740-24-3
Molecular Weight:
193.24
UNSPSC Code:
12352106
eCl@ss:
32160406
PubChem Substance ID:
24855739
NACRES:
NA.22
MDL number:
MFCD00002536

Key Documents

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Product Name

4-(Butylamino)benzoic acid, 97%

SMILES string

CCCCNc1ccc(cc1)C(O)=O

InChI

1S/C11H15NO2/c1-2-3-8-12-10-6-4-9(5-7-10)11(13)14/h4-7,12H,2-3,8H2,1H3,(H,13,14)

InChI key

YCCRFDDXAVMSLM-UHFFFAOYSA-N

assay

97%

form

powder

reaction suitability

reaction type: solution phase peptide synthesis

mp

149-151 °C (lit.)

application(s)

peptide synthesis

Quality Level

100

Related Categories

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKCX7141
MKCM3393
MKCF4051
MKBS0590V
MKBQ0242V

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R Murtaza et al.
Journal of pharmacological and toxicological methods, 46(3), 131-136 (2002-08-17)
The purpose of the present study was to develop a simple method for the simultaneous determination of mepivacaine, tetracaine, and p-butylaminobenzoic acid (BABA) in human plasma using high-performance liquid chromatography (HPLC) with a multiwavelength detector. Human blood samples containing heparin
Miranda de Jager et al.
Pharmaceutical research, 23(5), 951-960 (2006-05-23)
The objective of this study was to evaluate the utility of a stratum corneum substitute (SCS) as a novel in vitro percutaneous penetration model. The SCS consists of synthetic stratum corneum (SC) lipids (cholesterol, free fatty acids, and specific ceramides)
K Kudo et al.
Forensic science international, 116(1), 9-14 (2000-12-19)
Blood concentrations of tetracaine and its metabolite, p-butylaminobenzoic acid, were measured after spinal anesthesia with tetracaine which had been administered to patients under going orthopedic surgery. Tetracaine, an ester anesthetic, was given to 10 patients, the dose was 8-14mg, and
G N Menon et al.
Journal of pharmaceutical sciences, 70(5), 569-570 (1981-05-01)
A high-performance liquid chromatographic method was developed for the simultaneous determination of tetracaine hydrochloride and its hydrolytic degradation product, p-n-butylaminobenzoic acid. Separation was achieved using a mu Bondapak C18 column and the eluent, water-acetonitrile-methanol (60:20:20), containing 0.06% (v/v) sulfuric acid
Simultaneous determination of chlorhexidine, tetracaine and their degradation products by ion-pair liquid chromatography.
M Bauer et al.
Journal of chromatography, 315, 457-464 (1984-12-19)

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