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416444

Sigma-Aldrich

3-(Boc-amino)-1-propanol

97%

Synonym(s):

tert-Butyl N-(3-hydroxypropyl)carbamate

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About This Item

Linear Formula:
(CH3)3COC(O)NHCH2CH2CH2OH
CAS Number:
58885-58-8
Molecular Weight:
175.23
Beilstein/REAXYS Number:
1860807
MDL number:
MFCD00191883
UNSPSC Code:
12352200
PubChem Substance ID:
24866076
NACRES:
NA.22

assay

97%

form

liquid

reaction suitability

reagent type: cross-linking reagent

refractive index

n20/D 1.453

density

1.025 g/mL at 20 °C (lit.)

functional group

Boc
amine
hydroxyl

SMILES string

OCCCNC(OC(C)(C)C)=O

InChI

1S/C8H17NO3/c1-8(2,3)12-7(11)9-5-4-6-10/h10H,4-6H2,1-3H3,(H,9,11)

InChI key

XDJCYKMWJCYQJM-UHFFFAOYSA-N

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Application

Amine protected, difunctional reagent employed in the synthesis of phosphatidyl ethanolamines and ornithine.

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

228.2 °F - closed cup

flash_point_c

109 °C - closed cup

ppe

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Synthetic Communications, 21, 359-359 (1991)
Synthesis, 133-133 (1993)
Lan Yao et al.
Polymers, 12(5) (2020-05-28)
Polymeric nanomaterials made from amphiphilic block copolymers are increasingly used in the treatment of tumor tissues. In this work, we firstly synthesized the amphiphilic block copolymer PBnMA-b-P(BAPMA-co-PEGMA) via reversible addition-fragmentation chain transfer (RAFT) polymerization using benzyl methacrylate (BnMA), poly (ethylene

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