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535303

Sigma-Aldrich

(7-Azabenzotriazol-1-yloxy)tripyrrolidinophosphonium hexafluorophosphate

96%, for peptide synthesis

Sinônimo(s):

(3-Hydroxy-3H-1,2,3-triazolo[4,5-b]pyridinato-O)tri-1-pyrrolidinyl-phosphorus hexafluorophosphate, PyAOP

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About This Item

Fórmula empírica (Notação de Hill):
C17H27F6N7OP2
Número CAS:
156311-83-0
Peso molecular:
521.38
Número MDL:
MFCD03703417
Código UNSPSC:
12352101
ID de substância PubChem:
329757954
NACRES:
NA.22

Nome do produto

(7-Azabenzotriazol-1-yloxy)tripyrrolidinophosphonium hexafluorophosphate, 96%

Nível de qualidade

100

Ensaio

96%

adequação da reação

reaction type: Coupling Reactions

pf

163-168 °C (lit.)

aplicação(ões)

peptide synthesis

temperatura de armazenamento

−20°C

cadeia de caracteres SMILES

F[P-](F)(F)(F)(F)F.C1CCN(C1)[P+](On2nnc3cccnc23)(N4CCCC4)N5CCCC5

InChI

1S/C17H27N7OP.F6P/c1-2-11-21(10-1)26(22-12-3-4-13-22,23-14-5-6-15-23)25-24-17-16(19-20-24)8-7-9-18-17;1-7(2,3,4,5)6/h7-9H,1-6,10-15H2;/q+1;-1

chave InChI

CBZAHNDHLWAZQC-UHFFFAOYSA-N

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Categorias relacionadas

Aplicação

Reagent for synthesis of:
Cyclic RGC pentapeptides for functionalization through click chemistry
Fluorescent glucose bioprobes
ReactIR™ flow cell

Reagent for:
Disulfide bond engineering
Heteroaryl ether synthesis
Optimization of conformational constraint on non-phosphorylated cyclic peptide antagonists of the Grb2-SH2 domain

Informações legais

Sold under agreement with PE Biosystems
ReactIR is a trademark of Mettler-Toledo, Inc.

Pictogramas

Exclamation mark
GHS07

Palavra indicadora

Warning

Frases de perigo

H315,H319,H335

Classificações de perigo

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

Órgãos-alvo

Respiratory system

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Equipamento de proteção individual

dust mask type N95 (US), Eyeshields, Gloves

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Certificados de análise (COA)

Lot/Batch Number
MKCP1064
WXBD3533V
MKCM8637
MKCK0069
MKCF4696

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Zhaoguan Wu et al.
Scientific reports, 7, 46206-46206 (2017-04-08)
O-Acetylation of sialic acid in protein N-glycans is an important modification and can occur at either 4-, 7-, 8- or 9-position in various combinations. This modification is usually labile under alkaline reaction conditions. Consequently, a permethylation-based analytical method, which has
Si Liu et al.
Journal of proteomics, 181, 225-237 (2018-04-27)
Colorectal cancer (CRC) has become one of the most common cancers worldwide and the fifth most prevalent cancer in China with an upward trend in incidence rates. Altered glycosylation significantly affects the structural and functional changes in immunoglobulin G (IgG)
Yike Wu et al.
Analytical and bioanalytical chemistry, 409(16), 4027-4036 (2017-04-19)
A rapid and sensitive N-glycan profiling strategy for MALDI-MS incorporating the use of deglycosylation with microwave assistance and the co-derivatization of glycosylamine labeling with tris(2,4,6-trimethoxyphenyl)phosphonium acetic acid N-hydroxysuccinimide ester (TMPP-Ac-OSu) and methylamidation has been developed in this work. Notably, highly
Chang Wang et al.
Analytica chimica acta, 1002, 50-61 (2018-01-08)
Quantitative analysis of glycans is an emerging field in glycomic research. Herein we present a rapid and effective dual-labeling strategy, in the combination of isotopic derivatization of N-glycosylamine-based glycans by d0/d5-benzoyl chloride and methylamidation of sialic acids, to relatively quantify
Tarshona Stevens et al.
International journal of medicinal chemistry, 2012, 730239-730239 (2012-01-01)
The purpose of this study is to understand the interactions of some antibacterial cationic amphipathic cyclooctapeptides with calcium(II) and their secondary structural preferences. The thermodynamic parameters associated with calcium(II) interactions, between the antibacterial active cyclooctapeptides (COP 1-6) and those that
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Global Trade Item Number

SKUGTIN
535303-1G4061826732977
535303-5G4061832565118

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