1-(2-Bromoacetoxy)-2,5-pyrrolidinedione

Names

[ CAS No. ]:
42014-51-7

[ Name ]:
1-(2-Bromoacetoxy)-2,5-pyrrolidinedione

[Synonym ]:
N-SucciniMidyl BroMoacetate
2,5-Dioxopyrrolidin-1-yl 2-bromoacetate
(2,5-dioxopyrrolidin-1-yl) 2-bromoacetate
Bromoacetic acid N-hydroxysuccinimide ester
2,5-Pyrrolidinedione, 1-((bromoacetyl)oxy)-
MFCD00058571
1-(2-Bromoacetoxy)pyrrolidine-2,5-dione
Bromoacetic Acid N-Succinimidyl Ester
1-(2-Bromoacetoxy)-2,5-pyrrolidinedione
N-(Bromoacetoxy)succinimide
2,5-Pyrrolidinedione, 1-[(2-bromoacetyl)oxy]-

Chemical & Physical Properties

[ Density]:
1.9±0.1 g/cm3

[ Boiling Point ]:
291.7±42.0 °C at 760 mmHg

[ Melting Point ]:
115-116ºC

[ Molecular Formula ]:
C₆H₆BrNO₄

[ Molecular Weight ]:
236.020

[ Flash Point ]:
130.2±27.9 °C

[ Exact Mass ]:
234.948013

[ PSA ]:
63.68000

[ LogP ]:
-1.11

[ Appearance of Characters ]:
powder

[ Vapour Pressure ]:
0.0±0.6 mmHg at 25°C

[ Index of Refraction ]:
1.566

[ Storage condition ]:
−20°C

[ Water Solubility ]:
acetone: 25 mg/mL

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xi

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26-S36

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2925190090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

DownStream

Customs

[ HS Code ]: 2925190090

[ Summary ]:
2925190090 other imides and their derivatives; salts thereof VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0%

Articles

Preparation of peptide-protein immunogens using N-succinimidyl bromoacetate as a heterobifunctional crosslinking reagent.

Anal. Biochem. 155 , 95-102, (1986)

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...

Production of antibodies against degradative neoepitopes in aggrecan.

Methods Mol. Med. 100 , 237-50, (2004)

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. P...

Conjugation of synthetic peptides to proteins: quantitation from S-carboxymethylcysteine released upon acid hydrolysis.

Anal. Biochem. 187(1) , 136-40, (1990)

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 rea...