Saltar al contenido
MilliporeSigma
Todas las fotos(1)

Documentos clave

Ver Toda la documentación

749613

Sigma-Aldrich

4-(4,6-Dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium tetrafluoroborate

97%

Sinónimos:

DMTMM, MMTM

Iniciar sesiónpara Ver la Fijación de precios por contrato y de la organización
Todas las fotos(1)

About This Item

Fórmula empírica (notación de Hill):
C10H17BF4N4O3
Peso molecular:
328.07
MDL number:
MFCD11045040
UNSPSC Code:
12352005
PubChem Substance ID:
329766006
NACRES:
NA.22

assay

97%

form

solid

mp

202-207 °C

functional group

ether

SMILES string

F[B-](F)(F)F.COc1nc(OC)nc(n1)[N+]2(C)CCOCC2

InChI

1S/C10H17N4O3.BF4/c1-14(4-6-17-7-5-14)8-11-9(15-2)13-10(12-8)16-3;2-1(3,4)5/h4-7H2,1-3H3;/q+1;-1

InChI key

LCRXDNPNQMIQFZ-UHFFFAOYSA-N

Application

4-(4,6-Dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium tetrafluoroborate (DMTMM BF4) can be used as a coupling reagent alternative to DMTMM Cl in peptide synthesis because of its stability. It is also used in the synthesis of:
  • Esters and peptides in both solution and solid-phase.
  • γ-aminobutyric acid (GABA)-containing cyclic heptapeptide, unguisin A.
  • The cyclization of linear tetrapeptides.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

Elija entre una de las versiones más recientes:

Certificados de análisis (COA)

Lot/Batch Number
MKCQ2477
MKCN8786
MKCJ5692
MKCJ5694
MKCG9717

¿No ve la versión correcta?

Si necesita una versión concreta, puede buscar un certificado específico por el número de lote.

Busque por un COA

¿Ya tiene este producto?

Encuentre la documentación para los productos que ha comprado recientemente en la Biblioteca de documentos.

Visite la Librería de documentos

George Lo Huang et al.
Nanomaterials (Basel, Switzerland), 9(5) (2019-05-12)
Indoleamine 2,3-dioxygenase (IDO) is an immunomodulating enzyme that is overexpressed in many cancers with poor prognosis. IDO suppresses T cell immunity by catabolizing tryptophan into kynurenine (KYN), which induces apoptosis in T effector cells and enhances T regulatory cells, providing
Xiaoqin Zhang et al.
Carbohydrate polymers, 247, 116749-116749 (2020-08-25)
To enhance the drug delivery efficiency of hyaluronic acid (HA), we designed and prepared glycodendron and pyropheophorbide-a (Ppa)-functionalized HA (HA-Ppa-Dendron) as a nanosystem for cancer photodynamic therapy. Linear Ppa-modified HA (HA-Ppa) was also prepared as a control. Cellular uptake of
An improved process for the synthesis of DMTMM-based coupling reagents
Raw SA
Tetrahedron Letters, 50(8), 946-948 (2009)
Total synthesis of unguisin A
Hunter L and Chung JH
The Journal of Organic Chemistry, 76(13), 5502-5505 (2011)
Maria Laura Alfieri et al.
Antioxidants (Basel, Switzerland), 9(3) (2020-03-22)
The ability of gelatin-based hydrogels of incorporating and releasing under controlled conditions 5,6-dihydroxyindole-2-carboxylic acid (DHICA), a melanin-related metabolite endowed with marked antioxidant properties was investigated. The methyl ester of DHICA, MeDHICA, was also tested in view of its higher stability
Ver todos los artículos relacionados

Nuestro equipo de científicos tiene experiencia en todas las áreas de investigación: Ciencias de la vida, Ciencia de los materiales, Síntesis química, Cromatografía, Analítica y muchas otras.

Póngase en contacto con el Servicio técnico