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Merck

34490

Sigma-Aldrich

Dibutylamin

puriss., ≥99.0% (GC)

Synonym(e):

N-Butyl-1-butanamine, n-Dibutylamine, Di-n-butylamine

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About This Item

Lineare Formel:
(CH3CH2CH2CH2)2NH
CAS-Nummer:
Molekulargewicht:
129.24
Beilstein:
506001
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352100
PubChem Substanz-ID:
NACRES:
NA.22

Dampfdichte

4.46 (vs air)

Qualitätsniveau

Dampfdruck

1.9 mmHg ( 20 °C)

Qualität

puriss.

Assay

≥99.0% (GC)

Selbstzündungstemp.

594 °F

Expl.-Gr.

10 %

Brechungsindex

n20/D 1.417 (lit.)
n20/D 1.417

bp

159 °C (lit.)

mp (Schmelzpunkt)

−62 °C (lit.)

Löslichkeit

water: soluble 3.8 g/L at 20 °C

Dichte

0.767 g/mL at 25 °C (lit.)

Funktionelle Gruppe

amine

SMILES String

CCCCNCCCC

InChI

1S/C8H19N/c1-3-5-7-9-8-6-4-2/h9H,3-8H2,1-2H3

InChIKey

JQVDAXLFBXTEQA-UHFFFAOYSA-N

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Anwendung

Dibutylamine was employed as organocatalyst during the synthesis of 2-amino-3-cyano-4H-chromen-4-ylphosphonates via Knoevenagel, Pinner and phospha-Michael reactions. Di-n-butylamine (Dibutylamine) may be used to investigate the performance of a dry sampler, with an impregnated denuder in series with a glass fibre filter for airborne isocyanates. It was used in the preparation of 1M dibutylammonium phosphate buffer.

Signalwort

Danger

Gefahreneinstufungen

Acute Tox. 2 Inhalation - Acute Tox. 3 Dermal - Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1A

Lagerklassenschlüssel

3 - Flammable liquids

WGK

WGK 1

Flammpunkt (°F)

104.9 °F - closed cup

Flammpunkt (°C)

40.5 °C - closed cup

Persönliche Schutzausrüstung

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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1 of 2

Daniel Gylestam et al.
The Annals of occupational hygiene, 58(1), 28-49 (2013-08-21)
The performance of a dry sampler, with an impregnated denuder in series with a glass fibre filter, using di-n-butylamine (DBA) for airborne isocyanates (200ml min(-1)) is investigated and compared with an impinger flask with a glass fibre filter in series
Reddi Mohan Naidu Kalla et al.
European journal of medicinal chemistry, 76, 61-66 (2014-02-27)
A series of 2-amino-3-cyano-4H-chromen-4-ylphosphonates have been synthesized by reacting substituted salicylaldehydes, malononitrile, and dialkylphosphites using a catalytic amount of dibutylamine as an organocatalyst employing Knoevenagel, Pinner, and phospha-Michael reactions simultaneously in ethanol. This protocol is an environmentally friendly procedure and
C M Stobba-Wiley et al.
Journal of AOAC International, 83(4), 837-846 (2000-09-20)
A method was developed and validated for determination and quantitation of tilmicosin residues in swine, cattle, and sheep edible tissues, as well as chicken fat, skin, and muscle over a concentration range of 0.025 microg/g-20 microg/g. For chicken kidney and
Stefan Schmid et al.
Environmental science & technology, 46(7), 4067-4073 (2012-03-17)
Plasma air purifying systems present an interesting alternative to filters for purifying air. In this study, molecular processes in a commercially available ac driven plasma air purifier were studied in detail. This air purifier is supposed to reduce all air
A A Tohamy et al.
Mutation research, 360(3), 155-163 (1996-08-08)
The protective role of soybean feeding against the cytogenetic and histopathologic effects of the nitrosamine precursors sodium nitrate and dibutylamine was evaluated. Treated animals were killed every 3 months, over a period of 15 months, and bone marrow cells were

Artikel

Knoevenagel Condensation is an organic reaction named after Emil Knoevenagel. It is a classic C-C bond formation reaction and a modification of the Aldol Condensation.

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