345547
Hydrogen chloride solution
4.0 M in dioxane
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제품정보 (DICE 배송 시 비용 별도)
실험식(Hill 표기법):
HCl
CAS 번호:
Molecular Weight:
36.46
NACRES:
NA.21
PubChem Substance ID:
UNSPSC Code:
12352301
MDL number:
Concentration:
3.80-4.40 M (by NaOH, titration), 4.0 M in dioxane
Form:
liquid
form
liquid
Quality Level
concentration
3.80-4.40 M (by NaOH, titration), 4.0 M in dioxane
density
1.05 g/mL at 25 °C
SMILES string
Cl
InChI
1S/ClH/h1H
InChI key
VEXZGXHMUGYJMC-UHFFFAOYSA-N
General description
Hydrogen chloride solution contains 4.0 M hydrogen chloride in 1,4-dioxane as the solvent. It is commonly used as a deprotection reagent during the deprotection of the tert-butoxycarbonyl (Boc) group of various amino acids and peptides. Additionally, it serves as a reagent in various organic synthesis reactions, including the synthesis of N-9-Fluorenylmethoxycarbonyl- (Fmoc) amino-acid chlorides.
Application
Hydrogen chloride solution (4.0 M in dioxane) can be used as:
- A reagent for the deprotection of the N-Boc protecting group from various heterocyclic derivatives.
- A reagent for the deprotection of polymer protecting groups. For instance, deprotection of benzyl ether-protected polymer.
- A polymerization initiator in combination with ZnCl2 in the synthesis of formyl terminated poly(ethyl vinyl ether) from ethyl vinyl ether (EVE).
signalword
Danger
Hazard Classifications
Carc. 1B - Eye Irrit. 2 - Flam. Liq. 2 - Met. Corr. 1 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
supp_hazards
저장 등급
3 - Flammable liquids
flash_point_f
62.6 °F - closed cup
flash_point_c
17 °C - closed cup
Fast, efficient and selective deprotection of the tert-butoxycarbonyl (Boc) group using HCl/dioxane (4 m)
G H, et al.
The Journal of Peptide Research, 4, 338-341 (2001)
Preparation of N-9-fluorenylmethoxycarbonylamino acid chlorides from mixed anhydrides by the action of hydrogen chloride 1
FRANCIS C MF, et al.
International Journal of Peptide and Protein Research, 38, 97-102 (1991)
Surface-and redox-active multifunctional polyphenol-derived poly (ionic liquid) s: controlled synthesis and characterization
Patil N, et al.
Macromolecules, 49(20), 7676-7691 (2016)