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ChemicalBook > Product Catalogue >Organic Chemistry >Carboxylic acids and derivatives >tert-Butyl 3-(2-hydroxyethoxy)propanoate

tert-Butyl 3-(2-hydroxyethoxy)propanoate

tert-Butyl 3-(2-hydroxyethoxy)propanoate Structure
  • ₹0
  • Product name: tert-Butyl 3-(2-hydroxyethoxy)propanoate
  • CAS: 671802-00-9
  • MF: C9H18O4
  • MW: 190.24
  • EINECS:
  • MDL Number:MFCD22056310
  • Synonyms:tert-Butyl 3-(2-hydroxyethoxy)propanoate;HO-PEG1-CH2CH2COOTBU;Hydroxy-PEG1-t-butyl ester;3-(2-Hydroxyethoxy)propanoic acid 1,1-dimethylethyl ester;3-(2-Hydroxyethoxy)propanoic acid tert-butyl ester;HO-PEG1-t-Butyl ester;OH-PEG1-CH2CH2COOtBu;Hydroxy-PEG1-(CH2)2-Boc
Manufacturer Product number Product description Packaging Price Updated Buy

Properties

Boiling point :274.0±15.0 °C(Predicted)
Density :1.031±0.06 g/cm3(Predicted)
storage temp. :2-8°C
pka :14.36±0.10(Predicted)
form :liquid
color :Yellowish
Water Solubility :Water: 100 mg/mL (525.65 mM)

Safety Information

Symbol(GHS): GHS hazard pictograms
Signal word: Warning
Hazard statements:
Code Hazard statements Hazard class Category Signal word Pictogram P-Codes
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.
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-t-butyl ester is a PEG linker containing a hydroxyl group with a t-butyl ester. 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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