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Sigma-Aldrich

1-Iodbutan

99%, contains copper as stabilizer

Synonym(e):

Butyliodid

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About This Item

Lineare Formel:
CH3(CH2)3I
CAS-Nummer:
542-69-8
Molekulargewicht:
184.02
Beilstein:
1420755
MDL-Nummer:
MFCD00001098
UNSPSC-Code:
12352100
PubChem Substanz-ID:
24850205
NACRES:
NA.22

Dampfdichte

~5 (vs air)

Assay

99%

Form

liquid

Enthält

copper as stabilizer

Brechungsindex

n20/D 1.498 (lit.)

bp

130-131 °C (lit.)

mp (Schmelzpunkt)

−103 °C (lit.)

Löslichkeit

alcohol: soluble
diethyl ether: soluble
water: insoluble

Dichte

1.617 g/mL at 25 °C (lit.)

Funktionelle Gruppe

alkyl halide

SMILES String

CCCCI

InChI

1S/C4H9I/c1-2-3-4-5/h2-4H2,1H3

InChIKey

KMGBZBJJOKUPIA-UHFFFAOYSA-N

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Allgemeine Beschreibung

Thermal chemistry of 1-iodobutane has been investigated on clean and hydrogen- and deuterium-predosed Pt(111) single-crystal surfaces by temperature-programmed desorption and reflection-absorption infrared spectroscopy.

1-Iodobutane is an alkyl halide and is used as an electrophile during SN2 nucleophilic reaction.

Anwendung

1-Iodobutane was used in the synthesis of:
  • S-alkylated 5-(2-,3- and 4-methoxyphenyl)-4H-1,2,4-triazole-3-thiol
  • 5-(2-,3- and 4-methoxyphenyl)-4-phenyl-4H-1,2,4-triazole-3-thiol
  • N-butyl-N-methylpyrrolidinium bis(trifluoromethanesulfonyl)imide by reaction with 1-methylpyrrolidine in ethyl acetate

Piktogramme

FlameSkull and crossbones
GHS02,GHS06

Signalwort

Danger

H-Sätze

H226,H331

Gefahreneinstufungen

Acute Tox. 3 Inhalation - Flam. Liq. 3

Lagerklassenschlüssel

3 - Flammable liquids

WGK

WGK 3

Flammpunkt (°F)

91.4 °F - closed cup

Flammpunkt (°C)

33 °C - closed cup

Persönliche Schutzausrüstung

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

Hier finden Sie alle aktuellen Versionen:

Analysenzertifikate (COA)

Lot/Batch Number
MKCK3473
MKCF8881
MKCC2247
MKBV9911V
MKBT2903V

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Shin J-H, et al.
Electrochimica Acta, 50(19), 3859-3865 (2005)
Coro Echeverría et al.
Polymers, 11(4) (2019-04-10)
The work herein describes the preparation of thermoresponsive microgels with potential antimicrobial properties. Most of the work performed so far regarding microgels with antimicrobial activity, deals with the ability of microgels to carry and release antibiotics or antimicrobial agents (antimicrobial
L Labanauskas et al.
Farmaco (Societa chimica italiana : 1989), 59(4), 255-259 (2004-04-15)
New S-alkylated 5-(2-,3- and 4-methoxyphenyl)-4H-1,2,4-triazole-3-thiols (5a-c, 6a-c) and 5-(2-,3- and 4-methoxyphenyl)-4-phenyl-4H-1,2,4-triazole-3-thiols (7a-c, 8a-c, 9a-c) were synthesized by the alkylation of 3-(2-,3- and 4-methoxyphenyl)-4,5-dihydro-1H-1,2,4-triazole-5-thiones (3a-c) or 3-(2-,3- and 4-methoxyphenyl)-4-phenyl-4,5-dihydro-1H-1,2,4-triazole-5-thiones (4a-c) with 1-iodobutane or 1-(1,3-benzodioxol-5-yl)-2-bromo-1-ethanone, 2-bromo-1-(2,3-dihydro-1,4-benzodioxin-6-yl)-1-ethanone and 2-bromo-1-(3,4-dihydro-2H-1,5-benzodioxepin-7-yl)-1-ethanone. Compounds 3a-c and 4a-c
Ilkeun Lee et al.
The journal of physical chemistry. B, 109(7), 2745-2753 (2006-07-21)
The thermal chemistry of a number of C4 hydrocarbons (1,3-butadiene, 1-bromo-3-butene, 1-bromo-2-butene, trans-2-butene, cis-2-butene, 1-butene, 2-iodobutane, 1-iodobutane, and butane) was investigated on clean and hydrogen- and deuterium-predosed Pt(111) single-crystal surfaces by temperature-programmed desorption and reflection-absorption infrared spectroscopy. A combination of
Y Zea-Ponce et al.
Applied radiation and isotopes : including data, instrumentation and methods for use in agriculture, industry and medicine, 45(1), 63-68 (1994-01-01)
The benzodiazepine receptor tracer [123I]iomazenil (Ro 16-0154, IMZ) can be prepared in close to theoretical specific activity by the reaction of its tributyltin precursor (IMZ-SnBu3) with [123I]NaI in the presence of Iodogen. However, the labeling reaction is associated with variably
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