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38431

Sigma-Aldrich

N,N-Diisopropylmethylamine

≥98.0% (GC)

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Synonym(s):
N-Methyldiisopropylamine
Linear Formula:
[(CH3)2CH]2NCH3
CAS Number:
10342-97-9
Molecular Weight:
115.22
Beilstein:
1731609
MDL number:
MFCD00048281
PubChem Substance ID:
57649781
NACRES:
NA.22

Quality Level

100

Assay

≥98.0% (GC)

form

liquid

refractive index

n20/D 1.411 (lit.)

density

0.754 g/mL at 20 °C (lit.)

SMILES string

CC(C)N(C)C(C)C

InChI

1S/C7H17N/c1-6(2)8(5)7(3)4/h6-7H,1-5H3

InChI key

ISRXMEYARGEVIU-UHFFFAOYSA-N

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This Item
359378DX1545900690
N,N-Diisopropylmethylamine ≥98.0% (GC)

Sigma-Aldrich

38431

N,N-Diisopropylmethylamine

N-Isopropylmethylamine 98%

Sigma-Aldrich

359378

N-Isopropylmethylamine

N,N-Dimethylacetamide

Supelco

DX1545

N,N-Dimethylacetamide

N,N-Diisopropylethylamine purified by redistillation, ZerO2®, 99.5%

Sigma-Aldrich

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N,N-Diisopropylethylamine

form

liquid

form

liquid

form

liquid

form

liquid

refractive index

n20/D 1.411 (lit.)

refractive index

n20/D 1.384 (lit.)

refractive index

-

refractive index

n20/D 1.414 (lit.)

density

0.754 g/mL at 20 °C (lit.)

density

0.702 g/mL at 25 °C (lit.)

density

0.94 g/cm3 at 20 °C

density

0.742 g/mL at 25 °C (lit.)

Pictograms

FlameCorrosion
GHS02,GHS05

Signal Word

Danger

Hazard Statements

H225 - H314

Hazard Classifications

Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1B

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

50.0 °F - closed cup

Flash Point(C)

10 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Design, controlled synthesis, physico-chemical and biological characteristics of novel well-defined biodegradable star-shaped copolymers intended for advanced drug delivery is described. These new biocompatible star copolymers were synthesised by grafting monodispersed semitelechelic linear (sL) N-(2-hydroxypropyl)methacrylamide copolymers onto a 2,2-bis(hydroxymethyl)propionic acid (bisMPA)-based
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Protein-based self-assembled nanostructures hold tremendous promise as smart materials. One strategy to control the assembly of individual protein modules takes advantage of the directionality and high affinity bonding afforded by metal chelation. Here, we describe the use of 2,2'-bipyridine units

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