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Bromoacetamido-PEG4-t-Butyl Ester

Bromoacetamido-PEG4-t-Butyl Ester Structure
  • ₹0
  • Product name: Bromoacetamido-PEG4-t-Butyl Ester
  • CAS: 1807521-00-1
  • MF: C17H32BrNO7
  • MW: 442.34
  • EINECS:
  • MDL Number:MFCD28505519
  • Synonyms:Bromoacetamido-PEG4-t-Butyl Ester;Bromoacetamido-PEG5-t-Butyl Ester;BrCH2CONH-PEG4-COOtBu;CAS_1807521-00-1;Bromoacetamido-PEG4-C2-Boc;4,7,10,13-Tetraoxa-16-azaoctadecanoic acid, 18-bromo-17-oxo-, 1,1-dimethylethyl ester
Manufacturer Product number Product description Packaging Price Updated Buy

Properties

form :Liquid
color :Colorless to light yellow

Safety Information

Symbol(GHS): GHS hazard pictograms
Signal word: Warning
Hazard statements:
Code Hazard statements Hazard class Category Signal word Pictogram P-Codes
H302 Harmful if swallowed Acute toxicity,oral Category 4 Warning GHS hazard pictograms P264, P270, P301+P312, P330, P501
H315 Causes skin irritation Skin corrosion/irritation Category 2 Warning GHS hazard pictograms P264, P280, P302+P352, P321,P332+P313, P362
H319 Causes serious eye irritation Serious eye damage/eye irritation Category 2A Warning GHS hazard pictograms P264, P280, P305+P351+P338,P337+P313P
H335 May cause respiratory irritation Specific target organ toxicity, single exposure;Respiratory tract irritation Category 3 Warning GHS hazard pictograms
Precautionary statements:
P261 Avoid breathing dust/fume/gas/mist/vapours/spray.
P280 Wear protective gloves/protective clothing/eye protection/face protection.
P301+P312 IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.
P302+P352 IF ON SKIN: wash with plenty of soap and water.
P305+P351+P338 IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

Description

Bromoacetamido-PEG4-t-butyl ester is a PEG linker containing a bromide group and a t-butyl protected carboxyl group. The hydrophilic PEG spacer increases solubility in aqueous media. The bromide (Br) is a very good leaving group for nucleophilic substitution reactions. The t-butyl protected carboxyl group can be deprotected under acidic conditions.