330469
N-Phenylglycine
97%
Sinonimo/i:
(Phenylamino)acetic acid, Anilinoacetic acid
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Cambia visualizzazione
25 G
CHF 70.60
About This Item
Formula condensata:
C6H5NHCH2COOH
Numero CAS:
Peso molecolare:
151.16
Beilstein:
509838
Numero CE:
Numero MDL:
Codice UNSPSC:
12352209
ID PubChem:
NACRES:
NA.22
Prodotti consigliati
Livello qualitativo
Saggio
97%
Impiego in reazioni chimiche
reaction type: solution phase peptide synthesis
Punto di fusione
121-123 °C (lit.)
applicazioni
peptide synthesis
Stringa SMILE
OC(=O)CNc1ccccc1
InChI
1S/C8H9NO2/c10-8(11)6-9-7-4-2-1-3-5-7/h1-5,9H,6H2,(H,10,11)
NPKSPKHJBVJUKB-UHFFFAOYSA-N
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Categorie correlate
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
Eyeshields, Gloves, type N95 (US)
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I clienti hanno visto anche
A D Johnston et al.
Journal of dental research, 68(9), 1337-1344 (1989-09-01)
Using bond strength measurements, we investigated a number of related compounds in order to elucidate the role of the surface-active ingredient, N-phenylglycine (NPG), in experimental two-step and three-step bonding protocols resulting in adhesive bonding to dentin. All active compounds identified
Zhongqiao Hu et al.
The journal of physical chemistry. B, 113(48), 15851-15857 (2009-11-10)
A microscopic understanding of chiral separation mechanisms in liquid chromatography is significant in the pharmaceutical industry to facilitate the rational design of novel stationary phases and the optimization of separation processes. A molecular simulation study is reported to investigate the
Y Imai et al.
Dental materials : official publication of the Academy of Dental Materials, 10(4), 275-277 (1994-07-01)
This research was designed to study the effect of water or carboxylic acid monomer on the polymerization of 2-hydroxyethyl methacrylate (HEMA) in order to understand the bonding mechanism of dentin bonding systems using N-phenylglycine (NPG). The polymerization of HEMA in
J Watkins et al.
Trends in pharmacological sciences, 15(9), 333-342 (1994-09-01)
Metabotropic glutamate receptors represent a family of G protein-coupled receptors that can be activated by L-glutamate, the principal excitatory neurotransmitter in the brain. Until recently, progress in identifying the physiological and pathological roles of metabotropic glutamate receptors has been hampered
Mohamed A Elsawy et al.
Journal of peptide science : an official publication of the European Peptide Society, 18(5), 302-311 (2012-03-28)
We have been engaged in the microwave-solid phase peptide synthesis (SPPS) synthesis of the phenylglycine (Phg)-containing pentapeptide H-Ala-Val-Pro-Phg-Tyr-NH(2) (1) previously demonstrated to bind to the so-called BIR3 domain of the anti-apoptotic protein XIAP. Analysis of the target peptide by a
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