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TERT-BUTYL N,N-BIS(2-HYDROXYETHYL)CARBAMATE

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TERT-BUTYL N,N-BIS(2-HYDROXYETHYL)CARBAMATE Basic information

Product Name:
TERT-BUTYL N,N-BIS(2-HYDROXYETHYL)CARBAMATE
Synonyms:
  • TERT-BUTYL N,N-BIS(2-HYDROXYETHYL)CARBAMATE
  • N-BOC-DIETHANOLAMINE
  • BOC-DIETHANOLAMINE
  • Bis(2-hydroxyethyl)amine, N-BOC protected
  • tert-Butyl bis(2-hydroxyethyl)carbamate
  • N-Boc-diethanolamine >=98.0% (GC)
  • 1-Boc-diethanolamine
  • tert-Butyl bis(2-hydroxyethyl)
CAS:
103898-11-9
MF:
C9H19NO4
MW:
205.25
Mol File:
103898-11-9.mol
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TERT-BUTYL N,N-BIS(2-HYDROXYETHYL)CARBAMATE Chemical Properties

Boiling point:
324.2±35.0 °C(Predicted)
Density 
1.085 g/mL at 20 °C(lit.)
refractive index 
n20/D 1.461
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
pka
14.29±0.10(Predicted)
form 
Liquid or Oil
color 
Colorless
BRN 
4386562
InChI
InChI=1S/C9H19NO4/c1-9(2,3)14-8(13)10(4-6-11)5-7-12/h11-12H,4-7H2,1-3H3
InChIKey
KMUNFRBJXIEULW-UHFFFAOYSA-N
SMILES
C(OC(C)(C)C)(=O)N(CCO)CCO
CAS DataBase Reference
103898-11-9
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
10-21
HS Code 
2933998090

MSDS

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TERT-BUTYL N,N-BIS(2-HYDROXYETHYL)CARBAMATE Usage And Synthesis

Description

tert-butyl bis(2-hydroxyethyl)carbamate is a branched PEG with a tert-butyl protecting group and two hydroxyl end groups. The t-butyl group can be deprotected under acidic conditions. The hydroxyl group can react to further derivatize the compound. The hydrophilic PEG linker increases the water solubility of the compound in aqueous media.

Chemical Properties

Light yellow clear liquid

Uses

Building block for the synthesis of cationic lipids, nucleosides, etc.

reaction suitability

reagent type: cross-linking reagent

Synthesis

24424-99-5

111-42-2

103898-11-9

Under nitrogen protection, 2,2'-Azabisethanol (4.21 g, 40 mmol) was dissolved in acetonitrile (50 mL), and a solution of di-tert-butyl dicarbonate (Boc2O, 9.60 g, 44 mmol) in acetonitrile (50 mL) was slowly added. The reaction mixture was stirred at room temperature for 3.5 h. The solvent was removed by concentration under reduced pressure to afford tert-butyl bis(2-hydroxyethyl)carbamate as a colorless oil (8.20 g, 100% yield).

IC 50

Cleavable Linker; Alkyl/ether

References

[1] Bioorganic and Medicinal Chemistry Letters, 1997, vol. 7, # 24, p. 3135 - 3138
[2] Nucleosides and Nucleotides, 1999, vol. 18, # 2, p. 227 - 238
[3] Nucleosides, Nucleotides and Nucleic Acids, 2002, vol. 21, # 2, p. 111 - 123
[4] Bioorganic and Medicinal Chemistry, 2004, vol. 12, # 17, p. 4645 - 4665
[5] Patent: WO2014/12360, 2014, A1. Location in patent: Paragraph 00384

TERT-BUTYL N,N-BIS(2-HYDROXYETHYL)CARBAMATESupplier

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