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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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

FSL

Group 4: Flammable liquids
Type 3 petroleums
Hazardous rank III
Water insoluble liquid

JAN Code

140805-5G:
140805-VAR:
140805-100G:
140805-5KG:
140805-500G:
140805-10KG:
140805-BULK:

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Certificates of Analysis (COA)

Lot/Batch Number
MKCG8948
MKBZ4388V
MKBV8007V
MKBP0500V
MKBL4640V

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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
Mange R Yadav et al.
ACS omega, 3(9), 11802-11816 (2018-10-16)
Some quaternary gemini amphiphiles (GAs) were synthesized as nonviral gene delivery carriers. The critical miceller concentration values of these amphiphiles are indicative of their superior surface-active properties. All of the synthesized GAs, alone or along with lipids like cholesterol and/or
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
Merja J Poropudas et al.
Dalton transactions (Cambridge, England : 2003), 45(43), 17206-17215 (2016-11-02)
The reaction of 1-naphthyl bromide with n-butyl lithium, elemental tellurium, and 1,4-dibromobutane in THF affords both (C
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
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