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BPA diglycidyl ether

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Identification
Molecular formula
C21H24O4
CAS number
1675-54-3
IUPAC name
2-[[4-[1-methyl-1-[4-(oxiran-2-ylmethoxy)phenyl]ethyl]phenoxy]methyl]oxirane
State
State

At room temperature, BPA diglycidyl ether is typically a viscous liquid or semi-solid. It is often in this state due to its epoxy resin properties and applications.

Melting point (Celsius)
-25.00
Melting point (Kelvin)
248.15
Boiling point (Celsius)
276.00
Boiling point (Kelvin)
549.15
General information
Molecular weight
340.42g/mol
Molar mass
340.4190g/mol
Density
1.1700g/cm3
Appearence

BPA diglycidyl ether is a colorless to pale yellow liquid or semi-solid with a slight phenolic odor. It is a low-viscosity epoxy resin commonly used in industrial applications.

Comment on solubility

Solubility of 2-[[4-[1-methyl-1-[4-(oxiran-2-ylmethoxy)phenyl]ethyl]phenoxy]methyl]oxirane

The solubility of 2-[[4-[1-methyl-1-[4-(oxiran-2-ylmethoxy)phenyl]ethyl]phenoxy]methyl]oxirane (C21H24O4) can be influenced by various factors, including its molecular structure and the presence of functional groups. Generally, compounds with multiple aromatic and ether functionalities like this one tend to exhibit unique solubility characteristics.

Key Factors Influencing Solubility:

  • Polarity: The degree of polarity of the compound plays a crucial role. The presence of ether groups often enhances solubility in polar solvents.
  • Hydrophobic Interactions: The aromatic rings provide hydrophobic character, which might limit solubility in highly polar solvents.
  • Temperature: Temperature can also affect solubility; generally, increased temperature leads to greater solubility for many organic compounds.
  • pH Levels: The solubility of ionic or polar compounds can change with the pH of the solution, making this a significant consideration for this particular compound.

In summary, while 2-[[4-[1-methyl-1-[4-(oxiran-2-ylmethoxy)phenyl]ethyl]phenoxy]methyl]oxirane may be expected to possess moderate solubility due to its ether groups, its specific solubility characteristics will depend heavily on the solvent used, temperature, and the pH of the solution. As one might say, “solubility is a complex dance of forces and interactions,” making thorough testing in different conditions essential for accurate assessments.

Interesting facts

Interesting Facts About 2-[[4-[1-methyl-1-[4-(oxiran-2-ylmethoxy)phenyl]ethyl]phenoxy]methyl]oxirane

The compound 2-[[4-[1-methyl-1-[4-(oxiran-2-ylmethoxy)phenyl]ethyl]phenoxy]methyl]oxirane is a fascinating example of a complex organic molecule, exhibiting significant structural and functional diversity. Here are some key points to consider:

  • Chemical Structure: This compound features not only an oxirane group, known for its reactivity, but also an ether linkage and two aromatic systems. Such structures can lead to unique properties, making them useful in various applications.
  • Applications: Compounds with similar structures often find their uses in pharmaceutical formulations, particularly as intermediates or active pharmaceutical ingredients, due to their ability to interact with biological systems.
  • Reactivity: The presence of the epoxide (oxirane) moiety makes this compound particularly reactive, engaging in nucleophilic ring-opening reactions. This reactivity can be harnessed for further synthetic transformations.
  • Sterical Size: The bulky groups in the structure suggest that it may influence its interaction with enzymes or receptors in biological systems, potentially affecting its pharmacokinetics and pharmacodynamics.
  • Research Interest: Due to its complex architecture, researchers are keen to study how variations in substituents can modify biological activity, making it a candidate for drug design and development.

As a scientist or student, exploring the implications of compounds like this one is crucial. Such explorations not only aid in understanding basic chemical principles but also open pathways to innovate in fields like medicinal chemistry and materials science. The potential applications are vast, and this compound exemplifies the beauty and complexity of organic chemistry.

Synonyms
BISPHENOL A DIGLYCIDYL ETHER
1675-54-3
BADGE
2,2-Bis(4-glycidyloxyphenyl)propane
Epoxide A
Epophen EL 5
Diglycidyl bisphenol A ether
DGEBPA
Dian diglycidyl ether
Diglycidyl bisphenol A
epi-Rez 510
2,2-Bis(4'-glycidyloxyphenyl)propane
Bpdge
DGEBA
Diglycidyl ether of bisphenol A
Diomethane diglycidyl ether
Dian-bis-glycidylether
4,4'-Isopropylidenediphenol diglycidyl ether
Epi-Rez 508
2,2-Bis(p-glycidyloxyphenyl)propane
Araldite GY 250
Diglycidyl diphenylolpropane ether
Bis(4-glycidyloxyphenyl)dimethylmethane
Diglycidyl ether of 4,4'-isopropylidenediphenol
BISPHENOL A DIGLYCIDYL ETHER RESIN
ERL-2774
Diglycidyl ether of 2,2-bis(p-hydroxyphenyl)propane
EP 274
2,2-Bis[4-(2,3-epoxypropoxy)phenyl]propane
D.E.R. 332
Bis(4-hydroxyphenyl)dimethylmethane diglycidyl ether
Diglycidyl ether of 2,2-bis(4-hydroxyphenyl)propane
NSC 5022
4,4'-Dihydroxydiphenyldimethylmethane diglycidyl ether
p,p'-Dihydroxydiphenyldimethylmethane diglycidyl ether
MFCD00080480
Oxirane, 2,2'-[(1-methylethylidene)bis(4,1-phenyleneoxymethylene)]bis-
2,2-Bis(4-hydroxyphenyl)propane diglycidyl ether
2,2-Bis[4-(glycidyloxy)phenyl]propane
4,4'-Bis(2,3-epoxypropoxy)diphenyldimethylmethane
2,2-Bis(p-(2,3-epoxypropoxy)phenyl)propane
2,2-Bis(4-(2,3-epoxypropyloxy)phenyl)propane
2,2-Bis(phenyl-4-glycidoxy)propane
F3XRM1NX4H
2,2-Bis(4-hydroxyphenyl)propane, diglycidyl ether
2,2-Bis(p-hydroxyphenyl)propane, diglycidyl ether
Propane, 2,2-bis(4-(2,3-epoxypropoxy)phenyl)-
2,2'-((1-Methylethylidene)bis(4,1-phenyleneoxymethylene))bisoxirane
2-[[4-[2-[4-(oxiran-2-ylmethoxy)phenyl]propan-2-yl]phenoxy]methyl]oxirane
4,4'-Isopropylidenebis(1-(2,3-epoxypropoxy)benzene)
CHEMBL258558
DTXSID6024624
2,2-Bis[p-(2,3-epoxypropoxy)phenyl]propane
BISPHENOL DIGLYCIDYL ETHER
CHEBI:34578
2,2-Bis(p-hydroxyphenyl)propane diglycidyl ether
NSC-5022
Propane, 2,2-bis(p-(2,3-epoxypropoxy)phenyl)-
Propane, 2,2-bis[p-(2,3-epoxypropoxy)phenyl]-
Oxirane, 2,2'-((1-methylethylidene)bis(4,1-phenyleneoxymethylene))bis-
2,2-bis(4-(2,3-epoxypropoxy)phenyl)propane
2,2-Bis[4-(2,3-epoxypropyloxy)phenyl]propane
4,4'-Isopropylidenebis[1-(2,3-epoxypropoxy)benzene]
DTXCID804624
Epotuf 37-140
CAS-1675-54-3
CCRIS 1965
Dian-bis-glycidylether [Czech]
HSDB 331
2,2-bis(4-(2,3-epoxypropoxy)phenyl)-propane
2,2-Bis(p-(2,3-epoxypropoxy)phenyl)-Propane
2,2-Bis[4-(2,3-epoxypropoxy)phenyl]-Propane
2,2-Bis[p-(2,3-epoxypropoxy)phenyl]-Propane
SR-01000597404
91384-80-4
EINECS 216-823-5
UNII-F3XRM1NX4H
GY 6010
Bisphenol A, diglycidyl ether
2,2'-[propane-2,2-diylbis(4,1-phenyleneoxymethylene)]dioxirane
Araldite B
Araldite F
2,2'-(PROPANE-2,2-DIYLBIS(4,1-PHENYLENEOXYMETHYLENE))DIOXIRANE
2-((4-(2-(4-(oxiran-2-ylmethoxy)phenyl)propan-2-yl)phenoxy)methyl)oxirane
Propane, 2,2-bis (p-(2,3-epoxypropoxy)phenyl)
2, diglycidyl ether
Spectrum5_001987
Bisphenol-A diglycidylether
4,3-epoxypropoxy)benzene]
D.E.R.trade mark 332
bisphenol-a diglycidyl ether
isphenol a, diglycidyl ether
SCHEMBL22121
BSPBio_001468
KBioGR_000188
KBioSS_000188
BISPHENOLFDIGLYCIDYLETHER
diglycidyl ether of bisphenol-A
2,3-epoxypropoxy)phenyl]propane
NIOSH/SL1998000
BCBcMAP01_000157
KBio2_000188
KBio2_002756
KBio2_005324
KBio3_000375
KBio3_000376
NSC5022
2,3-epoxypropyloxy)phenyl]propane
Bio1_000378
Bio1_000867
Bio1_001356
Bio2_000188
Bio2_000668
HMS1361J10
HMS1791J10
HMS1989J10
HMS3267P05
HMS3402J10
HMS3414L19
HMS3649C20
HMS3678L17
WLN: T3OTJ B1OR D- 2X
Bisphenol A diglycidyl ether, 85%
WDC60009
2,2-bis(4-glycidyloxypheny)propane
Tox21_202141
Tox21_303315
BDBM50241439
2, 2-Bis(4-glycidyloxyphenyl)propane
2, 2-Bis(p-glycidyloxyphenyl)propane
2,2-bis-(4-Glycidyloxyphenyl)propane
AKOS003609360
Bis(4-glycidyloxyphenyl)dimethyamethane
DB14083
FB18832
2, 2-Bis(4'-glycidyloxyphenyl)propane
2,2-[Bis(4-glycidyloxyphenyl)]propane
4,3-epoxypropoxy)diphenyldimethylmethane
IDI1_033938
NCGC00025114-02
NCGC00025114-03
NCGC00025114-04
NCGC00025114-05
NCGC00025114-06
NCGC00025114-07
NCGC00025114-08
NCGC00257039-01
NCGC00259690-01
AS-33346
BISPHENOL A DIGLYCIDYL ETHER [MI]
SY050157
BISPHENOL A DIGLYCIDYL ETHER [HSDB]
BISPHENOL A DIGLYCIDYL ETHER [IARC]
HY-108567
B1796
CS-0029179
NS00006998
SL19980000
4, 4'-Isopropylidenediphenol diglycidyl ether
D.E.R.(TM) 332, used as embedding medium
Propane,2-bis[(p-2,3-epoxypropoxy)phenyl]-
Propane,2-bis[4-(2,3-epoxypropoxy)phenyl]-
Propane,2-bis[p-(2,3-epoxypropoxy)phenyl]-
2,2-Bis[(p-2,3-epoxypropoxy)phenyl]-Propane
Bis[4-(2,3-epoxypropoxy)phenyl]-(2)-propane
p,p'-Dimethylmethylenediphenol diglycidyl ether
4,4'-Isopropylidene diphenol, diglycidyl ether-
Bisphenol A diglycidyl ether, analytical standard
Diglycidyl ether of 4, 4'-isopropylidenediphenol
EN300-7403894
2, 2-Bis(4-hydroxyphenyl)propane diglycidyl ether
2, 2-Bis(p-hydroxyphenyl)propane diglycidyl ether
2, 2-Bis(p-hydroxyphenyl)propane, diglycidyl ether
4,4'-Bis(2, 3-epoxypropoxy)diphenyldimethylmethane
Phenol, p,p'-dimethylmethylenebis-, diglycidyl ether
Q2080808
SR-01000597404-1
SR-01000597404-3
SR-01000597404-4
BRD-A16694057-001-01-9
BRD-A16694057-001-06-8
Diglycidyl ether of 2, 2-bis(4-hydroxyphenyl)propane
Diglycidyl ether of 2, 2-bis(p-hydroxyphenyl)propane
diglycidyl ether of 2,2-bis(p-hydroxyphenyl)-propane
4, 4'-Dihydroxydiphenyldimethylmethane diglycidyl ether
PROPANE, 2,2-BIS((P-2,3-EPOXYPROPOXY)PHENYL)-
2,2'-(2,2-PROPANEDIYLBIS(4,1-PHENYLENEOXYMETHYLENE))DIOXIRANE
2,2'-[(1-methylethylidene)bis(4,1-phenyleneoxymethylene)]bis-oxirane
2,2'-[(1-Methylethylidene)bis(4,1-phenyleneoxymethylene)]bisoxirane, 9CI
2-(4-{2-[4-(oxiran-2-ylmethoxy)phenyl]propan-2-yl}phenoxymethyl)oxirane
Oxirane,2'-[(1-methylethylidene)bis(4,1-phenyleneoxymethylene)]bis-
2,2''-(4,4''-(propane-2,2-diyl)bis(4,1-phenylene))bis(oxy)bis(methylene)dioxirane
2,2'-(PROPANE-2,2-DIYLBIS(BENZENE-4,1-DIYLOXYMETHANEDIYL))DIOXIRANE
2-[(4-(1-Methyl-1-[4-(2-oxiranylmethoxy)phenyl]ethyl)phenoxy)methyl]oxirane #
2-{[4-(2-{4-[(oxiran-2-yl)methoxy]phenyl}propan-2-yl)phenoxy]methyl}oxirane
4,4'-(1-Methylethylidene)bisphenol diglycidyl ether;2,2-Bis(4-hydroxyphenyl)propane diglycidyl ether;BADGE