The above product is Ality Chemical's strong item with best price, good quality and fast supply. Ality Chemical has been focusing on the research and production of this field for over 14 years. At the same time, we are always committed to providi
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Cas:1066-51-9
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inquiryOur Advantage Rich Experience Our products are sold all over Europe,North&South America, Sino-East, Asia and pacific area as well as Africa,we establish long term. Quality service Company cooperates with research institutes. We strictly con
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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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inquiry(Aminomethyl)phosphonic acid Basic information Product Name: (Aminomethyl)phosphonic acid Synonyms: AMINOMETHYLPHOSPHONATE;(Aminomethyl)phosphonic acid, 98 %;(Aminomethyl)phosphonic acid,99%;Aminomethyl phosphonic acid 100mg [1066-51-9];(Amino
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inquiryStock products, own laboratory Package:Grams, Kilograms Application:For R&D Transportation:According to customer request Port:Shanghai
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inquiryhigh purity lowest priceAppearance:solid or liquid Storage:in sealed air resistant place Package:drum and bag Application:for pharma use Transportation:by sea or air Port:Beijing or Guangzhou
Jinhua huayi chemical co., ltd. is dedicated to the development, production and marketing of chemicals. On the basis of equality and mutual benefit, and under the principle of customer first, credit first, quality first, we are ready to join hands
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inquiryAcmec is a leading manufacturer and supplier of biochemical reagents and life science products. We have over 40,000 items in stock (real-time inventory) and offer discounted prices to registered members of the online store ( www.acmec.com.cn ) Appea
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high purity lowest priceAppearance:solid or liquid Storage:in sealed air resistant place Package:Foil bag; Drum; Plastic bottle Application:Pharma;Industry;Agricultural Transportation:by sea or air Port:Beijing or Guangzhou
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inquiryHunan chemfish Pharmaceutical co.,Ltd.located in Lugu High-tech industral park ,Hunan province . with its own R&D center and more than 10000㎡manufacture plant . Chemfish owns 40 reactors from 1000L to 8000L. With complete auxiliary equipment as
(Aminomethyl)phosphonic acidAppearance:powder Storage:Store in dry, dark and ventilated place Package:depended Application:Aminomethanephosphonic acid is a degradation product of glyphosate (G765000), a herbicide. Transportation:by sea or by air
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inquiryFactory supply high purity low priceAppearance:solid or liquid Storage:sealed in cool and dry place Package:As customer's requested Application:Pharma Intermediate Transportation:by courier/air/sea Port:Any port in China
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inquirygood quality, competitive price, thoughtful after sale serviceAppearance:white powder Storage:Keep it in dry,shady and cool place Package:25kg,50kg,180kg,200kg,250kg,1000kg,customization Application:Pharma;Industry;Agricultural;chemical reaserch Tran
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inquiry"HANGZHOU TIANYE CHEMICALS Co.LTD , Located in Eastern Science and Innovation Park Hangzhou .We are a high-tech enterprise specialized in technical research and development, production, development and trade of chemical products. We supply Multiple s
We are committed to providing our customers with the best products and services at the most competitive prices.Appearance:crystalline powder Storage:Room temperature with sealed well Package:according to the clients requirement Application:Use as pri
(Aminomethyl)phosphonic acid cas 1066-51-9Appearance:white crystalline powder Storage:Store in dry, dark and ventilated place Package:25KG drum Application:intermediate Transportation:by air, by sea, by express
reagent grade ex stockAppearance:white or off-white crystalline powder Storage:Keep away of light,cool place Package:1L 5L 10L 25L bottle Application:pharma intermediate Transportation:by Fedex, ship or plane
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inquiryaminomethylphosphonic acid diethyl ester
Aminomethylphosphonic acid
Conditions | Yield |
---|---|
With hydrogenchloride In water for 16h; Reflux; | 100% |
In various solvent(s) at 37℃; for 6h; phosphodiesterase I on carboxymethyl cellulose, pH 8.8; Yield given; |
Conditions | Yield |
---|---|
With hydrogenchloride for 18h; Heating; | A 93% B 97% |
N-acetylaminomethylphosphonic acid
Aminomethylphosphonic acid
Conditions | Yield |
---|---|
With hydrogenchloride at 70 - 80℃; for 1h; | 96% |
In various solvent(s) at 37℃; for 6h; α-chymotrypsin on carboxymethyl cellulose, pH 7.8; Yield given; | |
With acetic acid In methanol; water |
(acetylaminomethyl)phosphonic acid diethyl ester
Aminomethylphosphonic acid
Conditions | Yield |
---|---|
With hydrogenchloride Heating; | 96% |
diphenyl [(([(phenylmethyl)oxy]carbonyl)amino)methyl]phosphonate
Aminomethylphosphonic acid
Conditions | Yield |
---|---|
With hydrogenchloride for 4h; Heating; | 94% |
Aminomethylphosphonic acid
Conditions | Yield |
---|---|
With epichlorohydrin | 90% |
Aminomethylphosphonic acid
Conditions | Yield |
---|---|
With hydrogenchloride at 95℃; for 6h; | 88% |
O,O-diethyl-N-ethoxycarbonylaminomethylphosphate
Aminomethylphosphonic acid
Conditions | Yield |
---|---|
With hydrogenchloride for 20h; Heating; | 84.7% |
N-(triphenylmethyl)methanimine
acetic anhydride
A
Aminomethylphosphonic acid
B
(iminobismethylene)bisphosphonic acid
Conditions | Yield |
---|---|
Stage #1: acetic anhydride With phosphonic Acid at 0 - 20℃; Stage #2: N-(triphenylmethyl)methanimine at 0℃; Stage #3: With hydrogenchloride; water for 8h; Reflux; | A 74% B 6 %Spectr. |
diethyl N-benzoyl-α-aminomethylphosphonate
Aminomethylphosphonic acid
Conditions | Yield |
---|---|
With hydrogenchloride for 20h; Heating; | 70% |
(diethoxyphosphinyl)methyl trifluoromethanesulfonate
Aminomethylphosphonic acid
Conditions | Yield |
---|---|
With ammonia In ethanol at 0℃; for 0.0833333h; | 70% |
Conditions | Yield |
---|---|
With potassium hydroxide | A 60% B n/a |
N-(triphenylmethyl)methanimine
acetic anhydride
A
Aminomethylphosphonic acid
B
nitrilo-tris(methylenephosphonic acid)
C
(iminobismethylene)bisphosphonic acid
Conditions | Yield |
---|---|
Stage #1: acetic anhydride With phosphonic Acid at 0 - 20℃; Stage #2: N-(triphenylmethyl)methanimine at 0℃; Stage #3: With hydrogenchloride; water for 8h; Reflux; | A 54% B 9 %Spectr. C 13 %Spectr. |
Conditions | Yield |
---|---|
Stage #1: hydroxymethylphosphonic acid With benzylamine; ruthenium trichloride at 165℃; for 3h; Stage #2: With water Stage #3: With hydrogen | 0% |
Stage #1: hydroxymethylphosphonic acid With formamide; ruthenium(II) bis(triphenylphosphine) dichloride at 180℃; for 1h; Stage #2: With water | 0% |
Stage #1: hydroxymethylphosphonic acid With acetamide; ruthenium(II) bis(triphenylphosphine) dichloride at 180℃; for 16h; Stage #2: With water | 0.7% |
Stage #1: hydroxymethylphosphonic acid With dibenzylamine; ruthenium trichloride at 165℃; for 3h; Stage #2: With water Stage #3: With hydrogen | 0% |
Stage #1: hydroxymethylphosphonic acid With dibenzylamine; osmium (III) chloride In N,N-dimethyl acetamide at 150℃; for 3h; Stage #2: With water Stage #3: With hydrogen | 0% |
di-tert-butyl (hydroxymethyl)phosphonate
Aminomethylphosphonic acid
Conditions | Yield |
---|---|
Stage #1: di-t-butyl hydroxymethylphosphonate With dibenzylamine; ruthenium(II) bis(triphenylphosphine) dichloride In N,N-dimethyl acetamide at 150℃; for 3h; Stage #2: With water Stage #3: With hydrogen | 0.3% |
N-(bromomethyl)phtalimide
triethyl phosphite
Aminomethylphosphonic acid
Conditions | Yield |
---|---|
und anschliessend mit wss.Bromwasserstoffsaeure; |
aminomethyl-phosphonic acid monoethyl ester
Aminomethylphosphonic acid
Conditions | Yield |
---|---|
With hydrogenchloride at 140℃; | |
In various solvent(s) at 37℃; for 6h; phosphodiesterase I on carboxymethyl cellulose, pH 8.8; Yield given; |
Conditions | Yield |
---|---|
With chloroform; phosphorus trichloride unter Ausschluss von Feuchtigkeit und anschliessendes Kochen mit Salzsaeure; | |
Stage #1: N-(hydroxymethyl)acetamide With phosphorus(III) oxide In acetonitrile at 80℃; for 1h; Stage #2: With trifluorormethanesulfonic acid In acetonitrile at 80℃; for 2h; Stage #3: With water; sodium hydroxide In acetonitrile at 100℃; for 2h; | |
With chloroform; phosphorus trichloride unter Ausschluss von Feuchtigkeit und anschliessendes Kochen mit Salzsaeure; |
Conditions | Yield |
---|---|
(i) N2H4, (ii) NaNO2, aq. HCl, (iii) aq. HCl; Multistep reaction; |
Conditions | Yield |
---|---|
Yield given. Multistep reaction; |
Conditions | Yield |
---|---|
With trimethylsilyl bromide; water; triethyl phosphite 1.) 130-135 deg C, 12 h, 2.) room t., 5 h, 3.) 15 h, reflux; Yield given. Multistep reaction; |
diethyl (phthalimidomethyl)phosphonate
Aminomethylphosphonic acid
Conditions | Yield |
---|---|
With hydrogenchloride; hydrazine hydrate 1.) MeOH, overnight, room temp.; 2 h, reflux, 2.) 6 h, reflux; Multistep reaction; | |
With hydrogenchloride Yield given; |
N,N-methylenediacetamide
A
Aminomethylphosphonic acid
B
nitrilo-tris(methylenephosphonic acid)
Conditions | Yield |
---|---|
With hydrogenchloride; acetic acid; phosphorus trichloride 1) 1h, reflux 2) 12h, reflux; Yield given. Multistep reaction. Yields of byproduct given; |
nitrilo-tris(methylenephosphonic acid)
A
Aminomethylphosphonic acid
B
hydroxymethylphosphonic acid
C
(N,N-dimethylamino)methylphosphonic acid
Conditions | Yield |
---|---|
at 200℃; for 3h; Product distribution; 5 M HCl, sealed ampul, other temperature (250 deg C); |
phosphonomethylimino-di-acetic acid
A
formic acid
B
Aminomethylphosphonic acid
C
N-methylaminomethanephosphonic acid
D
N-(phosphonemethyl)glycine
E
N-formyl-N-(phosphonomethyl)glycine
F
N,N-dimethyl-formamide
Conditions | Yield |
---|---|
With cobalt(II) sulfate; oxygen In water at 85℃; under 41371.8 Torr; Product distribution; Rate constant; Mechanism; var. temp., pressure and reagents; deuterium isotope effect; |
formaldehyd
hexamethylenetetramine
A
Aminomethylphosphonic acid
B
nitrilo-tris(methylenephosphonic acid)
C
(iminobismethylene)bisphosphonic acid
D
N-methyliminobis(methylphosphonic acid)
Conditions | Yield |
---|---|
With phosphoric acid Mechanism; Product distribution; |
Aminomethylphosphonic acid
acetic anhydride
N-acetylaminomethylphosphonic acid
Conditions | Yield |
---|---|
With acetic acid at 100℃; for 0.5h; | 96% |
for 2.5h; Heating; | 81% |
Aminomethylphosphonic acid
glyoxalic acid monohydrate
N-(phosphonemethyl)glycine
Conditions | Yield |
---|---|
96% | |
In water |
Conditions | Yield |
---|---|
With water; propionic acid at 100℃; for 0.5h; | 95% |
Aminomethylphosphonic acid
1,1,1,3,3,3-hexamethyl-disilazane
Tri-N,O,O-(trimethylsilyl)-aminomethylphosphonsaeure
Conditions | Yield |
---|---|
at 150 - 160℃; | 91% |
Yield given; |
Conditions | Yield |
---|---|
Stage #1: formaldehyd; Aminomethylphosphonic acid With N-ethyl-N,N-diisopropylamine In water; acetonitrile at 20℃; for 0.333333h; Mannich Aminomethylation; Stage #2: N-4-(4’-chlorobiphenyl)methyl vancomycin In water; acetonitrile at -10℃; for 12h; Mannich Aminomethylation; | 81% |
Conditions | Yield |
---|---|
Stage #1: formaldehyd; Aminomethylphosphonic acid With N-ethyl-N,N-diisopropylamine In water; acetonitrile at 20℃; for 0.333333h; Mannich Aminomethylation; Stage #2: N3-decylaminoethylvancomycin In water; acetonitrile at -10℃; for 4h; Mannich Aminomethylation; | 79% |
Stage #1: formaldehyd; Aminomethylphosphonic acid With N-ethyl-N,N-diisopropylamine In water; acetonitrile at 0℃; for 1h; Inert atmosphere; Stage #2: N3-decylaminoethylvancomycin In water; acetonitrile | 57% |
Aminomethylphosphonic acid
pivaloyl chloride
[(2,2-Dimethyl-propionylamino)-methyl]-phosphonic acid
Conditions | Yield |
---|---|
With triethylamine In 1,4-dioxane; water at 20℃; for 2h; | 78% |
Conditions | Yield |
---|---|
With water; butyric acid at 100℃; for 0.5h; | 76% |
Aminomethylphosphonic acid
8-bromoadenosine
{[6-amino-9-((2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyltetrahydrofuran-2-yl)-9H-purin-8-ylamino]methyl}phosphonic acid
Conditions | Yield |
---|---|
With potassium carbonate In water at 100℃; for 48h; | 75% |
Conditions | Yield |
---|---|
Stage #1: formaldehyd; Aminomethylphosphonic acid; 3′-(methylthio)propyl vancomycin With N-ethyl-N,N-diisopropylamine In water; acetonitrile at -10℃; for 8h; Stage #2: trifluoroacetic acid | 72% |
Aminomethylphosphonic acid
S-methylisothiourea hydrochloride
guanidinomethanephosphonic acid
Conditions | Yield |
---|---|
With potassium hydroxide at 60℃; for 4h; | 70.1% |
Aminomethylphosphonic acid
di-tert-butyl dicarbonate
Conditions | Yield |
---|---|
With triethylamine In tetrahydrofuran; water for 72h; Ambient temperature; | 61% |
Aminomethylphosphonic acid
(3R)-4-tert-butoxy-3-[(tert-butoxycarbonyl)amino]-4-oxobutanoic acid
Boc-D-Asp(NH-CH2-PO3H2)-OBut
Conditions | Yield |
---|---|
With diphenyl phosphoryl azide; triethylamine In N,N-dimethyl-formamide at 0℃; for 96h; | 60% |
Aminomethylphosphonic acid
zinc(II) chloride
[Zn(aminomethylphosphonate)Cl]n
Conditions | Yield |
---|---|
In water stirred and heated at 70 °C for 1 h; filtered, crystd. by slow evapn. at ambient temp.; | 52% |
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