N-Succinimidyl bromoacetate

Base Information

Chemical Name:N-Succinimidyl bromoacetate
CAS No.:42014-51-7
Molecular Formula:C6H6 Br N O4
Molecular Weight:236.022
Hs Code.:2925190090
European Community (EC) Number:629-027-1
UNII:U5PMU8UHL8
DSSTox Substance ID:DTXSID90194821
Nikkaji Number:J441.016E
Wikidata:Q72451214
Mol file:42014-51-7.mol

Synonyms:N-succinimidyl bromoacetate

Suppliers and Price of N-Succinimidyl bromoacetate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Usbiological
N-Succinimidyl bromoacetate
50mg
$ 389.00

TRC
N-Succinimidyl Bromoacetate
1g
$ 585.00

TCI Chemical
N-Succinimidyl Bromoacetate >98.0%(GC)
100mg
$ 80.00

SynQuest Laboratories
N-Hydroxysuccinimidyl bromoacetate
1 g
$ 152.00

Soltec Ventures
N-Hydroxysuccinimidylbromoacetate
5gm
$ 680.00

Soltec Ventures
N-Hydroxysuccinimidylbromoacetate
1gm
$ 144.00

Sigma-Aldrich
Bromoacetic acid N-hydroxysuccinimide ester ≥95%, powder
250mg
$ 250.00

Sigma-Aldrich
Bromoacetic acid N-hydroxysuccinimide ester ≥95%, powder
100mg
$ 128.00

Sigma-Aldrich
Bromoacetic acid N-hydroxysuccinimide ester ≥95%, powder
1g
$ 752.00

Medical Isotopes, Inc.
N-Succinimidyl Bromoacetate
100 mg
$ 820.00

Total 39 raw suppliers

Chemical Property of N-Succinimidyl bromoacetate

Chemical Property:

Vapor Pressure:0.00191mmHg at 25°C
Melting Point:115-116oC
Boiling Point:291.7±42.0 °C(Predicted)
PSA：63.68000
Density:1.85±0.1 g/cm3(Predicted)
LogP:-0.07360
Storage Temp.:−20°C
Solubility.:acetone: 25 mg/mL
XLogP3:0
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:3
Exact Mass:234.94802
Heavy Atom Count:12
Complexity:224

Purity/Quality:

99%, ^*data from raw suppliers

N-Succinimidyl bromoacetate ^*data from reagent suppliers

Safty Information:

Pictogram(s): Xi
Hazard Codes:Xi
Statements: 36/37/38
Safety Statements: 26-36

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CC(=O)N(C1=O)OC(=O)CBr
Uses iodoacetate amine and sulfhydryl reactive homobifunctional cross-linking reagent 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.

Technology Process of N-Succinimidyl bromoacetate

There total 4 articles about N-Succinimidyl bromoacetate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 100.0%