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140805

Sigma-Aldrich

1,4-Dibromobutane

99%

Synonym(s):

Tetramethylene dibromide

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About This Item

Linear Formula:
Br(CH2)4Br
CAS Number:
110-52-1
Molecular Weight:
215.91
Beilstein:
1071199
EC Number:
203-775-5
MDL number:
MFCD00000261
UNSPSC Code:
12352100
PubChem Substance ID:
24848480
NACRES:
NA.22

Quality Level

200

Assay

99%

form

liquid

refractive index

n20/D 1.519 (lit.)

bp

63-65 °C/6 mmHg (lit.)

mp

−20 °C (lit.)

density

1.808 g/mL at 25 °C (lit.)

SMILES string

BrCCCCBr

InChI

1S/C4H8Br2/c5-3-1-2-4-6/h1-4H2

InChI key

ULTHEAFYOOPTTB-UHFFFAOYSA-N

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General description

1,4-Dibromobutane reaction with atactic poly(2-vinylpyridine) leads to the formation of long-range 3D molecular ordering in polymer chains.

Application

1,4-Dibromobutane was used to investigate the metabolism of two halopropanes: 1,3-dichloropropane and 2,2-dichloropropane. It was used as reagent during the synthesis of diazadioxa oxovanadium(IV) macrocyclic complexes.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2

Storage Class Code

10 - Combustible liquids

WGK

WGK 2

Flash Point(F)

>230.0 °F

Flash Point(C)

> 110 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Weijiang Guan et al.
Nature communications, 7, 11811-11811 (2016-06-03)
Inorganic dispersion is of great importance for actual implementation of advanced properties of organic-inorganic composites. Currently, electron microscopy is the most conventional approach for observing dispersion of inorganic fillers from ultrathin sections of organic-inorganic composites at the nanoscale by professional
M L Sharma et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 95, 562-568 (2012-05-15)
A new series of diazadioxa oxovanadium(IV) macrocyclic complexes of type [VO(mac)]SO(4) have been synthesized via the condensation reaction of a 3-(phenyl/substituted phenyl)-4-amino-5-hydrazino-1,2,4-triazole (H(2)L) with salicylaldehyde/2-hydroxyacetophenone and 1,4-dibromobutane in the presence of oxovanadium(IV) sulfate in ethanol. All the newly synthesized compounds
Qian Yu et al.
Guang pu xue yu guang pu fen xi = Guang pu, 24(2), 162-165 (2005-03-17)
In phene-50% NaOH medium, 1,4-dibromobutane reacts with carbazole (CZ) to form N-bromobutylcarbaole (BCZ) at 70-80 degrees C. The 2-thenoyl-2-carbazolyl-N-butyltrifluoroacetone (TCBTA) was synthesized by reaction of BCZ with 2-thenoyltrifluoroacetone (TTA) in acetone-K2CO3 medium at 50 degrees C. The TCBTA is a
Gautam Das et al.
Scientific reports, 9(1), 9572-9572 (2019-07-04)
Anion exchange membrane fuel cells (AEMFCs) have captivated vast interest due to non-platinum group metal catalysts and fuel flexibility. One of the major shortcomings of AEMFCs, however, is the lack of a stable and high anion conducting membrane. This study
W Onkenhout et al.
Drug metabolism and disposition: the biological fate of chemicals, 14(5), 608-612 (1986-09-01)
Two stable sulfur-containing metabolites were isolated from rat urine following administration of the mutagenic 1,4-dibromobutane. They were identified as tetrahydrothiophene and 3-hydroxysulfolane by gas chromatography and gas chromatography-mass spectrometry and were found to be excreted in 48-hr urine, representing 5.8
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