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F15803

Sigma-Aldrich

Formamidine acetate salt

99%

Synonym(s):

Formamidine acetic acid salt

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About This Item

Linear Formula:
HN=CHNH2 · CH3COOH
CAS Number:
Molecular Weight:
104.11
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

assay

99%

mp

158-161 °C (dec.) (lit.)

SMILES string

[H]C(N)=N.CC(O)=O

InChI

1S/C2H4O2.CH4N2/c1-2(3)4;2-1-3/h1H3,(H,3,4);1H,(H3,2,3)

InChI key

XPOLVIIHTDKJRY-UHFFFAOYSA-N

General description

Formamidine acetate salt is an organic compound commonly used as a reagent in the synthesis of heterocyclic compounds.

Application

Formamidine acetate salt is widely used in the preparation of formamidinium lead triiodide (FAPbI3) perovskites for perovskite solar cells. It is also used in the synthesis of formamidinium lead bromide nanocrystals for use as emitters in display applications.

pictograms

Exclamation mark

signalword

Warning

hcodes

pcodes

Hazard Classifications

Skin Sens. 1

Storage Class

11 - Combustible Solids

wgk_germany

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


Certificates of Analysis (COA)

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Monodisperse formamidinium lead bromide nanocrystals with bright and stable green photoluminescence
Protesescu L, et al.
Journal of the American Chemical Society, 138(43), 14202-14205 (2016)
Nanowire lasers of formamidinium lead halide perovskites and their stabilized alloys with improved stability
Fu Y, et al.
Nano Letters, 16(2), 1000-1008 (2016)
He Huang et al.
Nanomaterials (Basel, Switzerland), 10(1) (2020-01-08)
Metal halide perovskites are promising materials for a range of applications. The synthesis of light-emitting perovskite nanorods has become popular recently. Thus far, the facile synthesis of perovskite nanorods remains elusive. In this work, we have developed a facile synthesis
Additive-modulated evolution of HC (NH2) 2PbI3 black polymorph for mesoscopic perovskite solar cells
Wang Z, et al.
Chemistry of Materials, 27(20), 7149-7155 (2015)
An efficient metal catalyst free approach to synthesize 5-(4-(1, 2, 4, 5 tetrazin-3-yl) benzylamino)-5-oxopentanoic acid
Zewde, et al.
Tetrahedron Letters, 59, 3100-3103 (2018)

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