Passa al contenuto
Merck
Tutte le immagini(1)

Documenti

73200

Sigma-Aldrich

O-(4-Nitrobenzyl)hydroxylamine hydrochloride

≥98.5% (AT)

Sinonimo/i:

4-Nitrobenzyloxyamine hydrochloride

Autenticatiper visualizzare i prezzi riservati alla tua organizzazione & contrattuali
Tutte le immagini(1)

About This Item

Formula condensata:
O2NC6H4CH2ONH2 · HCl
Numero CAS:
2086-26-2
Peso molecolare:
204.61
Beilstein:
3709565
Numero CE:
218-228-6
Numero MDL:
MFCD00012954
Codice UNSPSC:
12352100
ID PubChem:
57652465
NACRES:
NA.22

Saggio

≥98.5% (AT)

Forma fisica

crystals

Punto di fusione

215 °C (dec.) (lit.)

Stringa SMILE

Cl.NOCc1ccc(cc1)[N+]([O-])=O

InChI

1S/C7H8N2O3.ClH/c8-12-5-6-1-3-7(4-2-6)9(10)11;/h1-4H,5,8H2;1H
LKCAFSOYOMFQSL-UHFFFAOYSA-N

Cerchi prodotti simili? Visita Guida al confronto tra prodotti

Categorie correlate

Altre note

Reagent for the preparation of N-(4-nitrobenzyloxy)-amino acids as substrates for an unambiguous N-hydroxypeptide synthesis

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)

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’.

Possiedi già questo prodotto?

I documenti relativi ai prodotti acquistati recentemente sono disponibili nell’Archivio dei documenti.

Visita l’Archivio dei documenti

I clienti hanno visto anche

Slide 1 of 3

1 of 3

O-tert-Butylhydroxylamine hydrochloride ≥99.0% (AT)

Sigma-Aldrich

20023

O-tert-Butylhydroxylamine hydrochloride

N-(Benzyloxycarbonyl)hydroxylamine 99%

Sigma-Aldrich

323276

N-(Benzyloxycarbonyl)hydroxylamine

N-Benzylhydroxylamine hydrochloride puriss., ≥99.0% (AT)

Sigma-Aldrich

13454

N-Benzylhydroxylamine hydrochloride

Joo Hyun Lim et al.
Frontiers in microbiology, 9, 2333-2333 (2018-10-16)
2-Deoxy-scyllo-inosose (DOI) has been a valuable starting natural product for the manufacture of pharmaceuticals or chemical engineering resources such as pyranose catechol. DOI synthase, which uses glucose-6-phosphate (Glc6P) as a substrate for DOI biosynthesis, is indispensably involved in the initial
B X Chen et al.
Mutation research, 273(3), 253-261 (1992-05-01)
The abasic site is one of the most frequent changes occurring in DNA and has been shown to be lethal and mutagenic. An abasic site in DNA can be tagged by reaction with O-4-nitrobenzylhydroxylamine (NBHA), resulting in the formation of
M Pauly et al.
Carbohydrate research, 282(1), 1-12 (1996-02-28)
An improved procedure has been developed for the rapid derivatization of oligosaccharides with UV-detectable p-nitrobenzylhydroxylamine (PNB). The improved conditions used result in quantitative derivatization of neutral oligosaccharides. Sialylated oligosaccharides can also be quantitatively PNB-derivatized without detectable desialylation. Of the oligosaccharides
T D Traylor et al.
Journal of chromatography, 272(1), 9-20 (1983-01-14)
A new quantitative procedure for the high-performance liquid chromatographic (HPLC) resolution of human brain gangliosides employing reversed-phase chromatography is described. To provide a derivative which can be determined by UV absorption techniques, p-nitrobenzyloxyamine was coupled to the gangliosides. Derivatization involves
T. Kolasa et al.
Tetrahedron, 30, 3591-3591 (1974)
Visualizza tutti i documenti correlati

Il team dei nostri ricercatori vanta grande esperienza in tutte le aree della ricerca quali Life Science, scienza dei materiali, sintesi chimica, cromatografia, discipline analitiche, ecc..

Contatta l'Assistenza Tecnica.