1,4-Dibromobutane, 98+%
1,4-Dibromobutane, 98+%
1,4-Dibromobutane, 98+%
Thermo Scientific Chemicals

1,4-Dibromobutane, 98+%

CAS: 110-52-1 | C4H8Br2 | 215.916 g/mol
Have Questions?
Change viewbuttonViewtableView
Quantity:
10 g
100 g
500 g
Catalog number A11669.22
also known as A11669-22
Price (USD)
32.65
Special offer
Online exclusive
Ends: 30-Jun-2026
37.80
Save 5.15 (14%)
Each
Quantity:
100 g
Request bulk or custom format
Price (USD)
32.65
Special offer
Online exclusive
Ends: 30-Jun-2026
37.80
Save 5.15 (14%)
Each
Chemical Identifiers
CAS110-52-1
IUPAC Name1,4-dibromobutane
Molecular FormulaC4H8Br2
InChI KeyULTHEAFYOOPTTB-UHFFFAOYSA-N
SMILESBrCCCCBr
View more
SpecificationsSpecification SheetSpecification Sheet
FormLiquid
Identification (FTIR)Conforms
Appearance (Color)Clear colorless to yellow
Assay (GC)≥98.0%
Refractive Index1.5165-1.5205 @ 20?C
1,4-Dibromobutane is used as an intermediate involved in the synthesis of active pharmaceutical ingredient and other organic compounds. It is also used in the investigation of metabolism of two halopropanes such as 1,3-dichloropropane and 2,2-dichloropropane. Further, it acts as a reagent to prepare diazadioxa oxovanadium(IV) macrocyclic complexes.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
1,4-Dibromobutane is used as an intermediate involved in the synthesis of active pharmaceutical ingredient and other organic compounds. It is also used in the investigation of metabolism of two halopropanes such as 1,3-dichloropropane and 2,2-dichloropropane. Further, it acts as a reagent to prepare diazadioxa oxovanadium(IV) macrocyclic complexes.

Solubility
Immiscible with water.

Notes
Incompatible with strong oxidizing agents and strong bases.
RUO – Research Use Only

General References:

  1. Chen, J.; Li, N.; Gao, Y.; Sun, F.; He, J.; Li, Y. Dual-responsive polypseudorotaxanes based on block-selected inclusion between polyethylene-block-poly(ethylene glycol) diblock copolymers and 1,4-diethoxypillar[5]arene. Soft matter 2015, 11 (39), 7835-7840.
  2. Stehouwer, J. S.; Goodman, M. M. Preparation of 1-tosyloxy-4-substituted-2-butenes using Ag(I) salts. Tetrahedron lett. 2015, 56 (30), 4480-4482.