B81255

N-Bromosuccinimide

99%, for peptide synthesis, ReagentPlus®

Manufacturer: Sigma Aldrich

CAS Number: 128-08-5

Synonym(S): NBS

Select a Size

Pack Size SKU Availability Price
5 G B81255-5-G In Stock ₹ 3,990.00
100 G B81255-100-G In Stock ₹ 5,430.00
250 G B81255-250-G In Stock ₹ 8,390.00
500 G B81255-500-G In Stock ₹ 15,940.00
1 KG B81255-1-KG In Stock ₹ 24,270.00
5 KG B81255-5-KG In Stock ₹ 50,120.00

B81255 - 5 G

₹ 3,990.00

In Stock

Quantity

1

Base Price: ₹ 3,990.00

GST (18%): ₹ 718.20

Total Price: ₹ 4,708.20

product name

N-Bromosuccinimide, ReagentPlus®, 99%

Quality Level

200

product line

ReagentPlus®

Assay

99%

form

powder

mp

175-180 °C (dec.) (lit.)

application(s)

peptide synthesis

storage temp.

2-8°C

SMILES string

BrN1C(=O)CCC1=O

InChI

1S/C4H4BrNO2/c5-6-3(7)1-2-4(6)8/h1-2H2

Other Options

Image Product Name Manufacturer Price Range
50-495-218
Chem-Impex International, Inc. N-Bromosuccinimide | 128-08-5 | MFCD00005510 | 100G
Chem-Impex International, Inc. ₹ 2,994.60
50-495-220
Chem-Impex International, Inc. N-Bromosuccinimide | 128-08-5 | MFCD00005510 | 1KG
Chem-Impex International, Inc. ₹ 6,160.32
50-495-219
Chem-Impex International, Inc. N-Bromosuccinimide | 128-08-5 | MFCD00005510 | 250G
Chem-Impex International, Inc. ₹ 3,721.86
50-165-6884
Sigma Aldrich Fine Chemicals Biosciences N-Bromosuccinimide ReagentPlus, 99, 128-08-5, MFCD00005510
Sigma Aldrich Fine Chemicals Biosciences ₹ 5,099.38
NC2126808
eMolecules​ N-Bromosuccinimide | 128-08-5 | MFCD00005510 | 100g
eMolecules​ ₹ 3,905.81
50-269-7959
eMolecules​ Combi-Blocks N-Bromosuccinimide 25g 296394254 QE-7736 97.000 128-08-5 MFCD00005510 177.985 C4H4BrNO2
eMolecules​ ₹ 2,854.28
8.01949
N-Bromosuccinimide
Sigma Aldrich ₹ 2,850.00 - ₹ 1,76,330.00
AR000YD3
2,5-Pyrrolidinedione, 1-bromo-
Aaron Chemicals LLC ₹ 342.24 - ₹ 1,283.40
CS-W008781
1-Bromo-2,5-pyrrolidinedione
ChemScene ₹ 1,283.40 - ₹ 20,705.52
AA43435
128-08-5 | N-Bromosuccinimide
A2B Chem ₹ 770.04 - ₹ 5,048.04

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Description

  • General description: N-Bromosuccinimide (NBS) is an organic compound commonly used as a brominating agent in organic synthesis. It is a convenient source of bromine radicals. It is used in radical bromination of allylic and benzylic positions. Additionally, NBS is also used as a reagent in electrophilic addition and electrophilic substitution reactions in organic chemistry.
  • Application: N-Bromosuccinimide can be used as a reagent:       In the Wohl-Ziegler reaction (bromination at allylic positions via a radical pathway).       To synthesize benzils and aliphatic 1,2-diketones from hydrobenzoins and 1,2-diols in the presence of CCl4 as a solvent.       To prepare tricyclic azepino[4,5-b]indoles from indole-β-enaminoesters or β-enaminones via Pictet–Spengler cyclization.To synthesize acylsilanes via oxidative hydrolysis of 2-silyl-1,3-dithianes.
  • Features and Benefits: NBS is an easier and safer brominating agent to handle than bromine.
  • Legal Information: ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

SAFETY INFORMATION

Pictograms

GHS03,GHS08,GHS05,GHS07,GHS09

Signal Word

Warning

Hazard Statements

H272,H290,H315,H317,H319,H341,H400

Precautionary Statements

P210 - P273 - P280 - P302 + P352 - P305 + P351 + P338 - P308 + P313

Hazard Classifications

Aquatic Acute 1 - Eye Irrit. 2 - Met. Corr. 1 - Muta. 2 - Ox. Sol. 3 - Skin Irrit. 2 - Skin Sens. 1B

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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175-180 °C (dec.) (lit.)

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peptide synthesis

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SMILES string:
BrN1C(=O)CCC1=O

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1S/C4H4BrNO2/c5-6-3(7)1-2-4(6)8/h1-2H2

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SMILES string:
CC(=O)O[C@H]1C(=O)[C@]2(C)[C@@H](O)C[C@H]3OC[C@@]3(OC(C)=O)[C@H]2[C@H](OC(=O)c4ccccc4)[C@]5(O)C[C@H](O)C(C)=C1C5(C)C

InChI:
1S/C31H38O11/c1-15-19(34)13-31(38)26(41-27(37)18-10-8-7-9-11-18)24-29(6,20(35)12-21-30(24,14-39-21)42-17(3)33)25(36)23(40-16(2)32)22(15)28(31,4)5/h7-11,19-21,23-24,26,34-35,38H,12-14H2,1-6H3/t19-,20-,21+,23+,24-,26-,29+,30-,31+/m0/s1

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SMILES string:
[Na+].O[C@@H]1[C@@H](O)[C@@H](O[C@@H]([C@H]1O)C([O-])=O)Oc2c[nH]c3ccc(Br)c(Cl)c23

InChI:
1S/C14H13BrClNO7.Na/c15-4-1-2-5-7(8(4)16)6(3-17-5)23-14-11(20)9(18)10(19)12(24-14)13(21)22;/h1-3,9-12,14,17-20H,(H,21,22);/q;+1/p-1/t9-,10-,11+,12-,14+;/m0./s1