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Merck
CN

672033

(S)-N-Boc-2,3-epoxypropylamine

97%

Synonym(s):

tert-Butyl (2S)-N-(2-oxiranylmethyl)carbamate

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About This Item

Empirical Formula (Hill Notation):
C8H15NO3
CAS Number:
Molecular Weight:
173.21
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352005
MDL number:
Assay:
≥96.5% (GCF), 97%
Form:
solid
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InChI

1S/C8H15NO3/c1-8(2,3)12-7(10)9-4-6-5-11-6/h6H,4-5H2,1-3H3,(H,9,10)/t6-/m0/s1

SMILES string

CC(C)(C)OC(=O)NC[C@H]1CO1

InChI key

ZBBGKXNNTNBRBH-LURJTMIESA-N

assay

≥96.5% (GCF), 97%

form

solid

optical purity

ee: ≥99.0% (GC)

mp

48-50 °C

functional group

amine, ether

Quality Level

Application

(S)-N-Boc-2,3-epoxypropylamine can be used:
  • To functionalize detonation nanodiamonds with NH2 functional group to enhance their optical properties.
  • In the synthesis of poly(ethylene glycol) (PEG) based block copolymers, which are further used in the preparation of micelles loaded with mRNA for intracellular mRNA delivery.

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Acute Tox. 4 Oral

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


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Guanidine-phosphate interactions stabilize polyion complex micelles based on flexible catiomers to improve mRNA delivery
Miyazaki T, et al.
European Polymer Journal, 140(1), 110028-110028 (2020)
Tandem malonate-based glucosides (TMGs) for membrane protein structural studies
Hussain H, et al.
Scientific reports, 7(1), 1-11 (2017)

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