Skip to Content
MilliporeSigma

P73005

Pyromellitic diimide

97%

Synonym(s):

Benzene-1,2,4,5-tetracarboxylic diimide, Reillex® 402

Slide 1 of 3
Sign In to View Organizational & Contract Pricing.

Select a Size

25 G

$226.00

100 G

$686.00

$226.00

Available to ship TODAYDetails

Request a Bulk Order
Ships Every 4 weeks

About This Item

Empirical Formula (Hill Notation):
C10H4N2O4
CAS Number:
2550-73-4
Molecular Weight:
216.15
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24898838
EC Number:
219-852-1
Beilstein/REAXYS Number:
214780
MDL number:
MFCD00005004

Key Documents

View All Documentation

Skip To

Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Product Name

Pyromellitic diimide, 97%

InChI key

UGQZLDXDWSPAOM-UHFFFAOYSA-N

InChI

1S/C10H4N2O4/c13-7-3-1-4-6(10(16)12-8(4)14)2-5(3)9(15)11-7/h1-2H,(H,11,13,15)(H,12,14,16)

SMILES string

O=C1NC(=O)c2cc3C(=O)NC(=O)c3cc12

assay

97%

form

powder

mp

>320 °C (lit.)

Quality Level

200

Looking for similar products? Visit Product Comparison Guide

Related Categories

Compare Similar Items

View Full Comparison

Show Differences

1 of 4

This Item
41228752449281391
Pyromellitic diimide 97%

Sigma-Aldrich

P73005

Pyromellitic diimide

Pyromellitic dianhydride 97%

Sigma-Aldrich

412287

Pyromellitic dianhydride

4,4′-Oxydiphthalic anhydride 97%

Sigma-Aldrich

524492

4,4′-Oxydiphthalic anhydride

Poly(4-vinylpyridine), cross-linked 2 % cross-linked with divinylbenzene

Sigma-Aldrich

81391

Poly(4-vinylpyridine), cross-linked

assay

97%

assay

97%

assay

97%

assay

-

mp

>320 °C (lit.)

mp

283-286 °C (lit.)

mp

225-229 °C (lit.)

mp

-

form

powder

form

powder

form

-

form

powder

Legal Information

Reillex is a registered trademark of Vertellus Specialties, Inc.

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
0000290149
0000290149
0000214560
0000214561
0000214561

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Shin-ichiro Kato et al.
The Journal of organic chemistry, 71(13), 4723-4733 (2006-06-17)
This paper reports the electroscopic and electrochemical properties of [2 + 2] pyromellitic diimide-based cyclophane 1 as well as acyclic N,N'-bis(2-methoxybenzyl)pyromellitic diimide 2 and the clathrate compounds formed by 1. Compound 1 was synthesized by direct cyclocondensation. Its structure was
Bijitha Balan et al.
Organic letters, 9(14), 2709-2712 (2007-06-07)
Complex formation of pyromellitic diimide derivatives with beta-cyclodextrin and anthracene-appended beta-cyclodextrin was studied with use of induced circular dichroism and 1H NMR spectroscopies. It is revealed that pyromellitic diimides form rim-binding type complexes with beta-CD and in these complexes the
Igor V Rubtsov et al.
Journal of the American Chemical Society, 126(9), 2684-2685 (2004-03-05)
We demonstrate for the first time the utility of time-resolved visible pump/mid-infrared (IR) probe spectroscopy to interrogate directly, and provide unique infomation regarding, conformationally dependent photoinduced ET dynamics and the subsequent structural evolution of the resulting charge-separated (CS) state. Exemplary
Z Váradyová et al.
Archiv fur Tierernahrung, 54(1), 33-46 (2002-02-20)
The effects of penicillin G, streptomycin, chloramphenicol, 2-bromoethanesulfonic acid and pyromellitic diimide on total gas, methane, volatile fatty acid production and food degradability after 24 h of incubation in vitro were investigated in the cultures of two rumen ciliates. The
Rocío García-Bueno et al.
Dalton transactions (Cambridge, England : 2003), 39(24), 5728-5736 (2010-05-25)
The hydroxo-complexes [Ni(2)(mcN(3))(2)(mu-OH)](2)(PF(6))(2)] [mcN(3) = 2,4,4-trimethyl-1,5,9-triazacyclododec-1-ene (Me(3)-mcN(3)) or 2,4,4,9-tetramethyl-1,5,9-triazacyclododec-1-ene (Me(4)-mcN(3))] react with imides (Him) in 1 : 2 (succinimide, glutarimide, saccharine and 1,8-naphthalimide) or 1 : 1 (pyromellitic diimide) molar ratio, leading to the formation of the imidate complexes: [Ni(mcN(3))(H(2)O)(Im)](+)
View All Related Papers

Questions

Reviews

No rating value

Active Filters

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service