B8271
Bromoacetic acid N-hydroxysuccinimide ester
≥95%, powder
Synonyma:
2,5-Dioxopyrrolidin-1-yl 2-bromoacetate, N-Hydroxysuccinimide bromoacetate
Přihlásit pro zobrazení organizačních a smluvních cen.
Vybrat velikost
Změnit zobrazení
| Velikost balení | Skladová položka | Dostupnost | Cena |
|---|---|---|---|
| 100 mg | Obraťte se na zákaznický servis a vyžádejte si informaci o dostupnosti. | 4 280,00 Kč | |
| 250 mg | Obraťte se na zákaznický servis a vyžádejte si informaci o dostupnosti. | 8 270,00 Kč | |
| 1 g | Obraťte se na zákaznický servis a vyžádejte si informaci o dostupnosti. | 24 800,00 Kč |
O této položce
Empirický vzorec (Hillův zápis):
C6H6BrNO4
Číslo CAS:
Molekulová hmotnost:
236.02
NACRES:
NC.07
PubChem Substance ID:
UNSPSC Code:
12352106
MDL number:
Assay:
≥95%
Form:
powder
4 280,00 Kč
Obraťte se na zákaznický servis a vyžádejte si informaci o dostupnosti.
Technický servis
Potřebujete pomoc? Náš tým zkušených odborníků je vám k dispozici.
Dovolte nám, abychom vám pomohliQuality Segment
assay
≥95%
form
powder
reaction suitability
reagent type: cross-linking reagent
solubility
acetone: 25 mg/mL, DMF: soluble
functional group
NHS ester
shipped in
dry ice
storage temp.
−20°C
SMILES string
O=C(N1OC(CBr)=O)CCC1=O
InChI
1S/C6H6BrNO4/c7-3-6(11)12-8-4(9)1-2-5(8)10/h1-3H2
InChI key
NKUZQMZWTZAPSN-UHFFFAOYSA-N
Application
A heterobifunctional cross-linking reagent which allows bromoacetylation of primary amine groups followed by coupling to sulfhydryl-containing compounds. Typically, initial reaction couples via ester to primary amine by amide bond formation in the pH range 6.5-8.5. The second reaction results in thioether bonding in pH range 7.0-8.0.
Disclaimer
The bromoacetyl group is light sensitive.
1 of 1
Tato položka | |||
|---|---|---|---|
| assay ≥95% | assay 98% | assay ≥97.0% (GC) | assay 98% |
| Quality Level 200 | Quality Level 200 | Quality Level 200 | Quality Level 200 |
| reaction suitability reagent type: cross-linking reagent | reaction suitability - | reaction suitability - | reaction suitability - |
| solubility acetone: 25 mg/mL, DMF: soluble | solubility water: insoluble | solubility water: insoluble | solubility - |
| form powder | form liquid | form - | form liquid |
| storage temp. −20°C | storage temp. - | storage temp. - | storage temp. - |
Skladovací třída
11 - Combustible Solids
wgk
WGK 3
ppe
dust mask type N95 (US), Eyeshields, Gloves
Vyberte jednu z posledních verzí:
Již tento produkt vlastníte?
Dokumenty související s produkty, které jste v minulosti zakoupili, byly za účelem usnadnění shromážděny ve vaší Knihovně dokumentů.
N Kolodny et al.
Analytical biochemistry, 187(1), 136-140 (1990-05-15)
A method described here for conjugating synthetic peptides to carrier proteins provides a convenient method for determining peptide-to-carrier protein ratios. N-Bromoacetyl-containing peptides are reacted in situ with carrier proteins in which the disulfide bonds were reduced with tri-n-butylphosphine. At pH
M S Bernatowicz et al.
Analytical biochemistry, 155(1), 95-102 (1986-05-15)
Synthetic peptides derived from human fibrin were unidirectionally conjugated to three carrier proteins (bovine serum albumin, bovine alpha-lactalbumin, and keyhole limpet hemocyanin) by a method that employs N-succinimidyl bromoacetate. This heterobifunctional crosslinking reagent was prepared with a 79% yield in
John S Mort et al.
Methods in molecular medicine, 100, 237-250 (2004-07-29)
The use of synthetic peptides to generate rabbit polyclonal anticatabolic neoepitope antibodies that can be used to study the presence of defined proteolytic cleavage sites in aggrecan is described. Principles of peptide design and methods for preparation and characterization of
Globální číslo obchodní položky
| Skladová položka | GTIN |
|---|---|
| B8271-250MG | 04061833442647 |
| B8271-100MG | 04061833287361 |
| B8271-1G | 04061833442630 |