86833
Tetrabutylammonium phosphate monobasic
puriss., 99% (T)
Synonym(s):
Tetrabutylammonium dihydrogen phosphate
Sign Into View Organizational & Contract Pricing
All Photos(4)
About This Item
Linear Formula:
(CH3CH2CH2CH2)4N[OP(OH)2O]
CAS Number:
Molecular Weight:
339.45
Beilstein:
5196532
EC Number:
MDL number:
UNSPSC Code:
12352116
PubChem Substance ID:
NACRES:
NA.21
Recommended Products
grade
puriss.
Quality Level
Assay
99% (T)
form
powder
mp
151-154 °C (lit.)
SMILES string
OP(O)([O-])=O.CCCC[N+](CCCC)(CCCC)CCCC
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
InChI key
ARRNBPCNZJXHRJ-UHFFFAOYSA-M
Looking for similar products? Visit Product Comparison Guide
Related Categories
General description
Tetrabutylammonium phosphate monobasic is a synthetic reagent. It can serve as a pH buffer in various chemical and biological applications.
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.
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Customers Also Viewed
Polymerisable squaramide receptors for anion binding and sensing.
Manesiotis P, et al.
Journal of Material Chemistry C, 2(42), 8990-8995 (2014)
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.
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
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
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
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service