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P4801

Sigma-Aldrich

Pentaerythritol tetrabromide

96%

Synonym(s):

Tetrakis(bromomethyl)methane

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About This Item

Linear Formula:
C(CH2Br)4
CAS Number:
3229-00-3
Molecular Weight:
387.73
Beilstein:
1679275
EC Number:
221-764-3
MDL number:
MFCD00000210
UNSPSC Code:
12352100
PubChem Substance ID:
24898499
NACRES:
NA.22

Assay

96%

form

crystals

bp

305-306 °C (lit.)

mp

158-160 °C (lit.)

density

2.596 g/mL at 25 °C (lit.)

SMILES string

BrCC(CBr)(CBr)CBr

InChI

1S/C5H8Br4/c6-1-5(2-7,3-8)4-9/h1-4H2

InChI key

OYSVBCSOQFXYHK-UHFFFAOYSA-N

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Application

Pentaerythritol tetrabromide is generally used as a flexible organic linker to build three-dimensional molecular frameworks such as dendrimers and metal-organic frameworks (MOFs). It can also be used in the synthesis of spiropentane, which is the simplest spiro-cycloalkane.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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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Synthesis of Imidazolium Oligomers with Planar and Stereo Cores and Their Antimicrobial Applications.
Yuan Y and Zhang Y
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A robust microporous metal-organic framework constructed from a flexible organic linker for acetylene storage at ambient temperature.
Xue Y S, et al.
Journal of Materials Chemistry, 22(20), 10195-10199 (2012)
Solvent-induced controllable synthesis, single-crystal to single-crystal transformation and encapsulation of Alq3 for modulated luminescence in (4, 8)-connected metal-organic frameworks.
Lan Y Q, et al.
Inorganic Chemistry, 51(14), 7484-7491 (2012)
Combined Electron-Diffraction and Spectroscopic Determination of the Structure of Spiropentane, C5H8.
Sandwisch J W, et al.
The Journal of Physical Chemistry A, 121(26), 4923-4929 (2017)
Chemistry of Spiropentane. I. An improved synthesis of spiropentane.
Applequist D E, et al.
The Journal of Organic Chemistry, 23(11), 1715-1716 (1958)

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