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471623

Sigma-Aldrich

1,1,1-Trimethylhydrazinium iodide

97%

Synonym(s):

1,1,1-Trimethylhydrazine iodide, N,N,N-Trimethylhydrazinium iodide, Trimethylhydrazonium iodide (6CI)

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About This Item

Linear Formula:
H2NN(CH3)3I
CAS Number:
3288-80-0
Molecular Weight:
202.04
MDL number:
MFCD00464984
UNSPSC Code:
12352100
PubChem Substance ID:
24870749
NACRES:
NA.22

Assay

97%

mp

225-230 °C (dec.) (lit.)

SMILES string

[I-].C[N+](C)(C)N

InChI

1S/C3H11N2.HI/c1-5(2,3)4;/h4H2,1-3H3;1H/q+1;/p-1

InChI key

HLNPDVKKRBWQAA-UHFFFAOYSA-M

Related Categories

General description

1,1,1-Trimethylhydrazinium iodide ([(CH3)3N-NH2]I, TMHI) is widely employed as a vicarious nucleophilic substitution (VNS) reagent for various aromatic amination reactions. On reaction with silver salt, it affords the following salts: nitrate (([(CH3)3N-NH2][NO3]), perchlorate ([(CH3)3N-NH2][ClO4]), azide ([(CH3)3N-NH2][N3]), 5-amino-1H-tetrazolate ([(CH3)3N-NH2][H2N-CN4]) and sulfate ([(CH3)3N-NH2]2[SO4].2H2O).

Application

1,1,1-Trimethylhydrazinium iodide (TMHI) may be employed for the amination of 1-X-3,5-dinitrobenzenes.

Pictograms

Health hazardExclamation mark
GHS08,GHS07

Signal Word

Danger

Hazard Statements

H315,H319,H335,H360

Hazard Classifications

Eye Irrit. 2 - Repr. 1B - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

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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Vladimir V Rozhkov et al.
The Journal of organic chemistry, 68(6), 2498-2501 (2003-03-15)
The amination of 1-X-3,5-dinitrobenzenes via the vicarious nucleophilic substitution of hydrogen (VNS) with 1,1,1-trimethylhydrazinium iodide (TMHI) in the presence of t-BuOK or NaOMe in DMSO was studied. It was observed (when X = OMe, OCH(2)CF(3), OCH(2)CF(2)CF(2)H, OPh) that the amination
Carles Miró Sabaté et al.
Chemistry, an Asian journal, 7(9), 2080-2089 (2012-06-29)
1,1,1-Trimethylhydrazinium iodide ([(CH(3))(3)N-NH(2)]I, 1) was reacted with a silver salt to form the corresponding nitrate ([(CH(3))(3)N-NH(2)][NO(3)], 2), perchlorate ([(CH(3))(3)N-NH(2)][ClO(4)], 3), azide ([(CH(3))(3)N-NH(2)][N(3)], 4), 5-amino-1H-tetrazolate ([(CH(3))(3)N-NH(2)][H(2)N-CN(4)], 5), and sulfate ([(CH(3))(3)N-NH(2)](2)[SO(4)]·2H(2)O, 6·2H(2)O) salts. The metathesis reaction of compound 6·2H(2)O with barium salts

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