Our perovskite materials include Spiro, MAPbI3, MAPbI2Cl, MAPbICl2, MAPbBrCl2, MAPbI2Cl, MAPbBr2I, MAPbBrI2, MAPbBr3, FAPbI3, FAPbBr3, Super PbI2, PbCI2, PbBr2, etc., Very often, you can see the publications in Science, Nature, Joule, Advanced Energ
high quality Appearance:White or off-white Solid Storage:Sealed, dry, microtherm , avoid light and smell. Package:According to the demand of customer Application:Organic synthesis Transportation:by air or by sea Port:shanghai
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inquiryHigh purity CAS 14965-49-2 methylammonium iodide in stock Our main business covers the fields below: 1.Noble Metal Catalysts (Pt.Pd...) 2.Organic Phosphine Ligands (Tert-butyl-phosphine.Cyclohexyl-phosphine...) 3.OLED intermediates (Flu
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inquiryWITH US,YOUR MONEY IN SAFE,YOUR BUSINESS IN SAFE 1)Quick Response Within 12 hours; 2)Quality Guarantee: All products are strictly tested by our QC, confirmed by QA and approved by third party lab in China, USA, Canada, Germany, UK, Italy, France et
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inquiryProduct Name: methylammonium iodide Synonyms: MAI;LT-S9126;methylammonium iodide;Methylamine·hydriodic acid;CH3NH3I (MAI);MethylazaniuM;Methanamine hydriodide;Methylamine Hydroiodide CAS: 14965-49-2 MF: CH6IN MW: 158.96951 EINEC
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inquiryMethylammonium iodide CAS 14965-49-2 Description Purity: 99% Min Application: Intermediates Appearance: Powder Package: Bag Delivery: 3-5days Our Advantage & Service 1.Top quality: Using high quality material and establishing a str
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inquiryProduct Details Grade: pharmaceutical grade Purity:99%+ ProductionCapacity: 1000 Kilogram/Month Scope of use: For scientific research only(The product must be used legally) Our Advantage 1. Best quality with competitive price. 2. Quick shipping,
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factory?direct?saleAppearance:White Powder Storage:Store In Dry, Cool And Ventilated Place Package:25kg/drum, also according to the clients requirement Application:It is widely used as a thickener, emulsifier and stabilizer Transportation:By Sea Or B
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inquirymethylamine
methylamine hydroiodide
Conditions | Yield |
---|---|
With hydrogen iodide In methanol; water at 0℃; for 2h; | 97% |
With hydrogen iodide; phosphorous acid In ethanol; water at 0℃; | 89% |
With hydrogen iodide In ethanol; water at 0℃; for 1h; | 87% |
triethylsilane
nitromethane
trimethylsilyl iodide
A
triethylsilyl iodide
B
Hexamethyldisiloxane
C
1,1,1-triethyl-3,3,3-trimethyl-disiloxane
D
hexaethyl disiloxane
E
methylamine hydroiodide
Conditions | Yield |
---|---|
Product distribution; Mechanism; 2 h at -5 deg C, then 5 h at 30 deg C; | A n/a B n/a C n/a D n/a E 80% |
methanol
6-methyl-[1,3,5]triazinane-2,4-dione
methyl iodide
A
methylamine hydroiodide
B
methylammonium carbonate
Conditions | Yield |
---|---|
at 120 - 130℃; |
B
methylamine hydroiodide
C
platinum
Conditions | Yield |
---|---|
In neat (no solvent) decomp. (207°C); thermal analysis; X-ray diffraction; |
Conditions | Yield |
---|---|
In methanol; water at 0℃; for 2h; | |
In water at 0℃; for 4h; | |
In ethanol; water at 20℃; for 2h; | |
In water |
methyl iodide
methylamine hydroiodide
Conditions | Yield |
---|---|
With hydrogen iodide In ethanol; water at 50℃; for 24h; |
formaldehyd
methylamine hydroiodide
Conditions | Yield |
---|---|
With ammonium iodide at 120 - 210℃; |
methylamine hydrochloride
methylamine hydroiodide
Conditions | Yield |
---|---|
With hydrogen iodide In ethanol; water at 0℃; for 2h; | |
With hydrogen iodide In ethanol at 50℃; for 0.0833333h; |
methanol
methylamine
A
isopropyl ammonium ion
B
methylamine hydroiodide
Conditions | Yield |
---|---|
With hydrogen iodide In water at 0℃; for 2h; |
Conditions | Yield |
---|---|
With hydrogen iodide In water |
Conditions | Yield |
---|---|
In dichloromethane; N,N-dimethyl-formamide | 100% |
sulfolane
methylamine hydroiodide
Conditions | Yield |
---|---|
at 80℃; for 0.5h; | 97% |
1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone
methylamine hydroiodide
Conditions | Yield |
---|---|
at 80℃; for 0.5h; | 96% |
CYANAMID
methylamine hydroiodide
Conditions | Yield |
---|---|
In water (Ar); dwelling (-10°C, 10 h); | 95% |
methylamine hydroiodide
N,N-dimethyl-formamide
Conditions | Yield |
---|---|
at 70℃; Glovebox; Inert atmosphere; | 94% |
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide under N2; stoich. amts.; soln. of alkylammonium salt and Pb salt in DMF at room temp.; soln. poured into nitromethane; | 90% |
In neat (no solvent) simultaneous deposition of MeNH3I and PbI2 on quartz substrate; | |
In further solvent(s) in γ-butyrolactone; obtained as a film on TiO2; |
Conditions | Yield |
---|---|
With HI In further solvent(s) solns. of SnI2 and org. compd. in aq. HI heated gently to 90.0°C(water/ethylene glycol bath); warm solns. mixed, pptn. on cooling to room temp.; filtration under N2 flow, ppt. dried (100°C, 5 h, Ar flow); | 67% |
In neat (no solvent, solid phase) at 200°C, solid state reaction, for several days; | |
In ethanol slow cooling (from 65 to 5°C) soln. SnI2 and MeNH3I (1:1) in EtOH; |
methylamine hydroiodide
hexylammonium iodide
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide under N2; stoich. amts.; alkylammonium salts dissolved in DMF at 35°C, Pb salt added, soln. stirred for 1 h; soln. poured into nitromethane, ppt. sepd. by centrifugation; | 60% |
methylamine hydroiodide
hexylammonium iodide
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide under N2; alkylammonium salts dissolved in DMF at 35°C, Pb salt added; ratio of C6H13NH3I:CH3NH3I:PbI2 = 2:3:3; soln. poured into nitromethane, ppt. sepd. by centrifugation; | 60% |
2-Aminomethylthiophene
methylamine hydroiodide
Conditions | Yield |
---|---|
Stage #1: methylamine hydroiodide; lead(II) iodide With hydrogen iodide; hypophosphorous acid In water at 0.9℃; for 0h; Stage #2: 2-Aminomethylthiophene With hydrogen iodide In water at 80℃; for 0.5h; | 60% |
Conditions | Yield |
---|---|
With H3PO2 In water 57 % aq. HI, heating at reflux temp.; soln. was cooled to ca. 20 °C, crystals were filtered, dried in air, elem. anal.; | 56% |
methylamine hydroiodide
hydrogen iodide
lead(II) acetate trihydrate
thiourea
Conditions | Yield |
---|---|
In water at 40 - 60℃; for 20h; Sealed tube; | 54% |
methylamine hydroiodide
Conditions | Yield |
---|---|
In water addn. of N2H4*2HCl to soln. of Pt-compd. in H2O, heating (60°C), cooling, addn. of org. compd. in H2O; addn. of EtOH, filtn., crystn. on standing (room temp., P4O10); elem. anal.; | A n/a B 50% |
methylamine hydroiodide
hydrogen iodide
lead(II) acetate trihydrate
thiourea
Conditions | Yield |
---|---|
In water at 40 - 60℃; for 20h; Sealed tube; | 47% |
methylamine hydroiodide
hydrogen iodide
lead(II) acetate trihydrate
thiourea
Conditions | Yield |
---|---|
In water at 40 - 60℃; for 20h; Sealed tube; | 42% |
methylamine hydroiodide
copper
Cu(CH3NH2)4I2
Conditions | Yield |
---|---|
In acetonitrile 1-1.5 h; elem. anal.; | 40% |
In methanol 1-1.5 h; elem. anal.; | 40% |
Conditions | Yield |
---|---|
Stage #1: hydrogen iodide; lead(II) oxide With hypophosphorous acid In water at 130℃; for 0.0833333 - 0.166667h; Stage #2: methylamine hydroiodide; 4-Aminomethylpiperidine In water at 240℃; for 0.0833333h; | 31.5% |
Conditions | Yield |
---|---|
Stage #1: hydrogen iodide; lead(II) oxide With hypophosphorous acid In water at 130℃; for 0.0833333 - 0.166667h; Stage #2: methylamine hydroiodide; 4-Aminomethylpiperidine In water at 240℃; for 0.0833333h; | 25.6% |
Conditions | Yield |
---|---|
Stage #1: hydrogen iodide; lead(II) oxide With hypophosphorous acid In water at 130℃; for 0.0833333 - 0.166667h; Stage #2: 3-Aminomethylpiperidine; methylamine hydroiodide In water at 240℃; for 0.0833333h; | 22.4% |
Conditions | Yield |
---|---|
Stage #1: hydrogen iodide; lead(II) oxide With hypophosphorous acid In water at 130℃; for 0.0833333 - 0.166667h; Stage #2: methylamine hydroiodide; 4-Aminomethylpiperidine In water at 240℃; for 0.0833333h; | 17.7% |
Conditions | Yield |
---|---|
Stage #1: hydrogen iodide; lead(II) oxide With hypophosphorous acid In water at 130℃; for 0.0833333 - 0.166667h; Stage #2: 3-Aminomethylpiperidine; methylamine hydroiodide In water at 240℃; for 0.0833333h; | 12.2% |
Conditions | Yield |
---|---|
Stage #1: hydrogen iodide; lead(II) oxide With hypophosphorous acid In water at 130℃; Stage #2: methylamine hydroiodide; 4-Aminomethylpiperidine With hydrogen iodide In water for 0.0833333h; Heating; | 12% |
Conditions | Yield |
---|---|
Stage #1: hydrogen iodide; lead(II) oxide With hypophosphorous acid In water at 130℃; for 0.0833333 - 0.166667h; Stage #2: 3-Aminomethylpiperidine; methylamine hydroiodide In water at 240℃; for 0.0833333h; | 11.2% |
Conditions | Yield |
---|---|
With ethanol at 50 - 60℃; |
methylamine hydroiodide
Conditions | Yield |
---|---|
With acetone; silver(I) iodide |
methylamine hydroiodide
Conditions | Yield |
---|---|
at -196.1℃; Irradiation; |
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