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Hydroxy-PEG1-CH2CO2tBu

Hydroxy-PEG1-CH2CO2tBu Structure
  • ₹0
  • Product name: Hydroxy-PEG1-CH2CO2tBu
  • CAS: 287174-32-7
  • MF: C8H16O4
  • MW: 176.21
  • EINECS:
  • MDL Number:MFCD27635155
  • Synonyms:Hydroxy-PEG1-CH2COOtBu;HO-PEG1-CH2COOtBu;Hydroxy-PEG1-CH2CO2tBu;Acetic acid, 2-(2-hydroxyethoxy)-, 1,1-dimethylethyl ester;Hydroxy-PEG1-CH2-Boc;tert-Butyl (2-hydroxyethoxy)acetate;Hydroxy-PEG1-t-butyl acetate;tert-butyl 2-(2-hydroxyethoxy)acetate(WXPC0081)
Manufacturer Product number Product description Packaging Price Updated Buy

Properties

Boiling point :257.0±15.0 °C(Predicted)
Density :1.048±0.06 g/cm3(Predicted)
form :liquid
pka :14.26±0.10(Predicted)
color :Colourless

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

Hydroxy-PEG1-CH2CO2tBu is a PEG linker containing a hydroxyl group with a t-butyl protected carboxyl group. The hydrophilic PEG spacer increases solubility in aqueous media. The hydroxyl group enables further derivatization or replacement with other reactive functional groups. The t-butyl protected carboxyl group can be deprotected under acidic conditions.

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