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416444

3-(Boc-amino)-1-propanol

Name: 3-(Boc-amino)-1-propanol
Brand: ALDRICH

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

UNSPSC Code:

12352200

NACRES:

NA.22

PubChem Substance ID:

24866076

MDL number:

MFCD00191883

Beilstein/REAXYS Number:

1860807

Assay:

97%

Form:

liquid

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Properties

Quality Level

200

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

Description

Application

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

Storage Class

10 - Combustible liquids

wgk

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)

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Synthetic Communications, 21, 359-359 (1991)

Construction of NIR Light Controlled Micelles with Photothermal Conversion Property: Poly(poly(ethylene glycol)methyl ether methacrylate) (PPEGMA) as Hydrophilic Block and Ketocyanine Dye as NIR Photothermal Conversion Agent.

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

Synthesis, 133-133 (1993)

Global Trade Item Number

SKU	GTIN
416444-10ML	04061838054081
416444-50ML	04061838127396