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279528

Sigma-Aldrich

1,3-Diiminoisoindoline

97%

Synonym(s):

1,3-Isoindolinediimine, Phthalimide diimide

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About This Item

Empirical Formula (Hill Notation):
C8H7N3
CAS Number:
3468-11-9
Molecular Weight:
145.16
Beilstein/REAXYS Number:
118477
EC Number:
222-426-8
MDL number:
MFCD00010062
UNSPSC Code:
12171500
PubChem Substance ID:
24856893
NACRES:
NA.47

Quality Level

100

assay

97%

form

powder or crystals

mp

~197 °C (dec.) (lit.)

application(s)

diagnostic assay manufacturing
hematology
histology

storage temp.

room temp

SMILES string

N=C1NC(=N)c2ccccc12

InChI

1S/C8H7N3/c9-7-5-3-1-2-4-6(5)8(10)11-7/h1-4H,(H3,9,10,11)

InChI key

RZVCEPSDYHAHLX-UHFFFAOYSA-N

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Related Categories

pictograms

CorrosionExclamation mark
GHS05,GHS07

signalword

Danger

Hazard Classifications

Eye Dam. 1 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

Certificates of Analysis (COA)

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Sergey M Borisov et al.
ACS applied materials & interfaces, 2(2), 366-374 (2010-02-27)
A new class of oxygen indicators is described. Platinum(II) and palladium(II) complexes of azatetrabenzoporphyrins occupy an intermediate position between tetrabenzoporphyrins and phthalocyanines and combine features of both. The new dyes are excitable in the red part of the spectrum and
Nathan J Yutronkie et al.
Materials (Basel, Switzerland), 12(8) (2019-04-27)
Efficient synthesis of silicon phthalocyanines (SiPc) eliminating the strenuous reaction conditions and hazardous reagents required by classical methods is described. Implementation into organic thin-film transistors (OTFTs) affords average electron field-effect mobility of 3.1 × 10-3 cm2 V-1 s-1 and threshold

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