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Documenti

262412

Sigma-Aldrich

4-(Butylamino)benzoic acid

97%, for peptide synthesis

Sinonimo/i:

p-Butylaminobenzoic acid

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About This Item

Formula condensata:
CH3(CH2)3NHC6H4CO2H
Numero CAS:
4740-24-3
Peso molecolare:
193.24
Numero MDL:
MFCD00002536
Codice UNSPSC:
12352106
eCl@ss:
32160406
ID PubChem:
24855739
NACRES:
NA.22

product name

4-(Butylamino)benzoic acid, 97%

Livello qualitativo

100

Saggio

97%

Forma fisica

powder

Impiego in reazioni chimiche

reaction type: solution phase peptide synthesis

Punto di fusione

149-151 °C (lit.)

applicazioni

peptide synthesis

Stringa SMILE

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)
YCCRFDDXAVMSLM-UHFFFAOYSA-N

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Pittogrammi

Exclamation mark
GHS07

Avvertenze

Warning

Indicazioni di pericolo

H315,H319,H335

Classi di pericolo

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

Organi bersaglio

Respiratory system

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves

Certificati d'analisi (COA)

Cerca il Certificati d'analisi (COA) digitando il numero di lotto/batch corrispondente. I numeri di lotto o di batch sono stampati sull'etichetta dei prodotti dopo la parola ‘Lotto’ o ‘Batch’.

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Acetaminofene United States Pharmacopeia (USP) Reference Standard

USP

1003009

Acetaminofene

4-(Aminomethyl)benzoic acid 97%

Sigma-Aldrich

283746

4-(Aminomethyl)benzoic acid

Alcool benzilico Pharmaceutical Secondary Standard; Certified Reference Material

Supelco

PHR1019

Alcool benzilico

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
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
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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