34500
Dibutylamine
purum, ≥98.0% (GC)
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About This Item
Linear Formula:
(CH3CH2CH2CH2)2NH
CAS Number:
Molecular Weight:
129.24
EC Number:
203-921-8
UNSPSC Code:
12352100
Beilstein/REAXYS Number:
506001
MDL number:
vapor density
4.46 (vs air)
vapor pressure
1.9 mmHg ( 20 °C)
grade
purum
assay
≥98.0% (GC)
autoignition temp.
594 °F
expl. lim.
10 %
refractive index
n20/D 1.417
bp
159 °C (lit.)
mp
−62 °C (lit.)
solubility
water: soluble 3.8 g/L at 20 °C
density
0.767 g/mL at 25 °C (lit.)
SMILES string
Cl.CCN=C=NCCCN(C)C, CCCCNCCCC
InChI
1S/C8H19N/c1-3-5-7-9-8-6-4-2/h9H,3-8H2,1-2H3
InChI key
JQVDAXLFBXTEQA-UHFFFAOYSA-N
Application
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.
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Danger
hcodes
Hazard Classifications
Acute Tox. 2 Inhalation - Acute Tox. 3 Dermal - Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1A
Storage Class
3 - Flammable liquids
wgk
WGK 1
flash_point_f
104.9 °F - closed cup
flash_point_c
40.5 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Regulatory Information
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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
T Sasaki et al.
Journal of chromatography. A, 888(1-2), 93-102 (2000-08-19)
This paper dealt with a simple and efficient method for separating a mixture of different series of ionic, high polar, and hydrophilic conjugates of bile acids by high-performance ion-pair chromatography (HPIPC) with a new volatile ion-pair chromatographic reagent, di-n-butylamine acetate