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227447

4,9-Dioxa-1,12-dodecanediamine

Name: 4,9-Dioxa-1,12-dodecanediamine
Brand: ALDRICH

99%

Synonym(s):

1,4-Bis(3-aminopropoxy)butane, 4,9-Dioxadodecanediamine

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About This Item

Linear Formula:

H₂N(CH₂)₃O(CH₂)₄O(CH₂)₃NH₂

CAS Number:

7300-34-7

Molecular Weight:

204.31

Beilstein:

1750788

EC Number:

230-745-9

MDL number:

MFCD00009802

UNSPSC Code:

12162002

PubChem Substance ID:

24853632

NACRES:

NA.23

Assay

99%

form

liquid

refractive index

n20/D 1.4609 (lit.)

bp

134-136 °C/4 mmHg (lit.)

density

0.962 g/mL at 25 °C (lit.)

SMILES string

NCCCOCCCCOCCCN

InChI

1S/C10H24N2O2/c11-5-3-9-13-7-1-2-8-14-10-4-6-12/h1-12H2

InChI key

YOOSAIJKYCBPFW-UHFFFAOYSA-N

Pictograms

GHS05,GHS07

Signal Word

Danger

Hazard Statements

H314,H317,H332

Precautionary Statements

P261 - P271 - P280 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338

Hazard Classifications

Acute Tox. 4 Inhalation - Eye Dam. 1 - Skin Corr. 1B - Skin Sens. 1A

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 1

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Design, RNA cleavage and antiviral activity of new artificial ribonucleases derived from mono-, di- and tripeptides connected by linkers of different hydrophobicity.

Nikolay Tamkovich et al.

Bioorganic & medicinal chemistry, 24(6), 1346-1355 (2016-02-24)

A novel series of metal-free artificial ribonucleases (aRNases) was designed, synthesized and assessed in terms of ribonuclease activity and ability to inactivate influenza virus WSN/A33/H1N1 in vitro. The compounds were built of two short peptide fragments, which include Lys, Ser

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