Tetrabutylammonium phosphate monobasic

Name: Tetrabutylammonium phosphate monobasic
Brand: SIAL

99% (T), powder, puriss

Sinónimos:

Tetrabutylammonium dihydrogen phosphate

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About This Item

Fórmula lineal:

(CH₃CH₂CH₂CH₂)₄N[OP(OH)₂O]

Número CAS:

5574-97-0

Peso molecular:

339.45

NACRES:

NA.21

PubChem Substance ID:

329769489

UNSPSC Code:

12352116

EC Number:

226-947-1

MDL number:

MFCD00064526

Beilstein/REAXYS Number:

5196532

Nombre del producto

Tetrabutylammonium phosphate monobasic, puriss., 99% (T)

InChI key

ARRNBPCNZJXHRJ-UHFFFAOYSA-M

InChI

1S/C16H36N.H3O4P/c1-5-9-13-17(14-10-6-2,15-11-7-3)16-12-8-4;1-5(2,3)4/h5-16H2,1-4H3;(H3,1,2,3,4)/q+1;/p-1

SMILES string

OP(O)([O-])=O.CCCC[N+](CCCC)(CCCC)CCCC

grade

puriss.

assay

99% (T)

form

powder

mp

151-154 °C (lit.)

Quality Level

100

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Categorías relacionadas

Phosphates

Application

Tetrabutylammonium phosphate monobasic is the suitable reagent used in the following studies:

Resolution of disaccharides reverse-phase ion-pairing HPLC (RPIP-HPLC).
Disaccharide analysis of ³⁵S- heparan sulfate (HS).
As folding buffer for the dissolution of desalted oligonucleotides.

It may be used as reagent for the analysis of tetrasaccharides and ³⁵S-disaccharides by HPLC. It may also be used in the preparation of monobasic tetrabutylammonium phosphate (TBAP) imprinted polymers.

General description

Tetrabutylammonium phosphate monobasic is a synthetic reagent. It can serve as a pH buffer in various chemical and biological applications.

Clase de almacenamiento

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Kinetics and mechanism of K+- and Na+-induced folding of models of human telomeric DNA into G-quadruplex structures.

Robert D Gray et al.

Nucleic acids research, 36(12), 4191-4203 (2008-06-24)

Cation-induced folding into quadruplex structures for three model human telomeric oligonucleotides, d[AGGG(TTAGGG)(3)], d[TTGGG(TTAGGG)(3)A] and d[TTGGG(TTAGGG)(3)], was characterized by equilibrium titrations with KCl and NaCl and by multiwavelength stopped flow kinetics. Cation binding was cooperative with Hill coefficients of 1.5-2.2 in

Role for 3-O-sulfated heparan sulfate as the receptor for herpes simplex virus type 1 entry into primary human corneal fibroblasts.

Vaibhav Tiwari et al.

Journal of virology, 80(18), 8970-8980 (2006-08-31)

Herpes simplex virus type 1 (HSV-1) infection of the corneal stroma remains a major cause of blindness. Primary cultures of corneal fibroblasts (CF) were tested and found susceptible to HSV-1 entry, which was confirmed by deconvolution imaging of infected cells.

Heparan sulfate D-glucosaminyl 3-O-sulfotransferase-3A sulfates N-unsubstituted glucosamine residues.

J Liu et al.

The Journal of biological chemistry, 274(53), 38155-38162 (1999-12-23)

3-O-Sulfation of glucosamine by heparan sulfate D-glucosaminyl 3-O-sulfotransferase (3-OST-1) is the key modification in anticoagulant heparan sulfate synthesis. However, the heparan sulfates modified by 3-OST-2 and 3-OST-3A, isoforms of 3-OST-1, do not have anticoagulant activity, although these isoforms transfer sulfate

Polymerisable squaramide receptors for anion binding and sensing.

Manesiotis P, et al.

Journal of Material Chemistry C, 2(42), 8990-8995 (2014)

Heparan sulfate 3-O-sulfotransferase isoform 5 generates both an antithrombin-binding site and an entry receptor for herpes simplex virus, type 1.

Guoqing Xia et al.

The Journal of biological chemistry, 277(40), 37912-37919 (2002-07-26)

Heparan sulfate 3-O-sulfotransferase transfers sulfate to the 3-OH position of a glucosamine residue of heparan sulfate (HS) to form 3-O-sulfated HS. The 3-O-sulfated glucosamine residue contributes to two important biological functions of HS: binding to antithrombin and thereby carrying anticoagulant

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