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Cas:5329-14-6
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inquiryItems Standard Result Purity(%) ≥99.5 99.68 Sulphate(%) ≤0.05 0.020
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inquiryProduct description: Product name Sulfamic acid CAS number 5329-14-6 Assay ≥99.5% Appearance White crystal Capacity 2000mt/year Application Sweeting agent,diionic cleaning ag
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inquiryProduct Name: Sulfamic acid Synonyms: SULFAMIC ACID, CERTIFIED, PRIMARY STANDARDSULFAMIC ACID, CERTIFIED, PRIMARY STANDARDSULFAMIC ACID, CERTIFIED, PRIMARY STANDARDSULFAMIC ACID, CERTIFIED, PRIMARY STANDARD;aminosulfuricacid;Imidosulfonic acid;Jum
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inquiryCAS 5329-14-6 Name Sulfamic acid Appearance White Crystals or Crystalline Powder Application Can be used as bleaching AIDS, also as herbicide, fire retardant
High purity Sulfamic Acid with high quality cas:5329-14-6 1. Guaranteed purity; 2. Large quantity in stock; 3. Largest manufacturer; 4. Best service after shipment with email; 5. High quality & competitive price; Appearance:White
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inquirySulfamic Acid CAS:5329-14-6 items standard result purity(%) ≥99.5 99.68 sulphate(%) ≤0.05 0.020 iron(%)
Appearance:white or yellowish white flaky crystal Storage:Keep the sun from direct sunlight ;prevention against high temperature Package:As customer request Application:Used for research and industrial manufacture. Transportatio
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inquirySuperior quality, moderate price & quick delivery. Appearance:white crystal powder Storage:Stored in cool, dry and ventilation place; Away from fire and heat Package:25kg/drum, or as per your request. Application:Used as Pharmaceutical Intermed
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inquiryProduct name: Sulfamic Acid CAS No.: 5329-14-6 Molecule Formula:H3NO3S Molecule Weight:97.09 Purity: 99.5% Package: 25kg/bag Description:White quadrature crystals Manufacture Standards:Enterprise Standard TESTING I
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inquiryAnsciep Chemical is a professional enterprise manufacturing and distributing fine chemicals and speciality chemicals. We have been dedicated to heterocycle compounds and phenyl rings for tens of years. This is our mature product for export. Our quali
Conditions | Yield |
---|---|
In sulfuric acid byproducts: CO2; urea dild. in 100% H2SO4 (stirring/cooling); addn. of small portions of fuming H2SO4 (temp. shouldn't exceed 45°C/stirring/cooling); heating carefully to 80°C; evolution of CO2; addn. of next portion fuming H2SO4 and repeating;; left for some time; filtration, washing (concd. H2SO4); drying on clay; left overnight in air; recrystn. from water;; | 94% |
In sulfuric acid heating with excess fuming H2SO4 (80-90°C, depending on SO3-content); vigorous reaction, evolution of heat;; |
Conditions | Yield |
---|---|
With air In melt two salts was reacted in melt in air; | A n/a B n/a C 92% |
Conditions | Yield |
---|---|
In water aq. acetoxim soln., containing liquid SO2, (25°C) left for 5 h in autoclave;; | 90% |
In water aq. acetoxim soln. cooled to -80°C; excess of SO2 condensed; sealing of tube; warming up to 0°C (pressure increases); left for 5.5 h at that temp.;; opened flask releases excess of SO2; filtration; dried by washing (alc., ether);; | 77% |
In ethanol; water acetoxim dild. in water/ethanol is satd. with SO2 gas (0°C); leftfor three days (0°C); (pptd. solid HSO3NH2 will be removed);; filtration, addn. of SO2; washing (alc., ether); dried in air;; | 76% |
In water aq. medium; dependence of pressure (1.14-3.52 kg/cm*cm more than atm.) and temp. (5-30°C); formation of liquid SO2 should be avoided; pptn.;; | |
In water aq. medium; dependence of pressure (1.14-3.52 kg/cm*cm more than atm.) and temp. (5-30°C); formation of liquid SO2 should be avoided; pptn.;; |
Conditions | Yield |
---|---|
In water byproducts: pyridine; diln. of C5H5NSO3 in ammonia water (10% NH3) under sepn. of pyridine;; extraction of pyridine (ether); evapn. (water bath); addn. of concd. H2SO4 (cooling); filtration; drying on clay; recrystn from water;; | 80% |
Conditions | Yield |
---|---|
In water byproducts: trimethylamine; diln. in ammonia water by short heating under sepn. of (CH3)N;; evapn.; removal of exceeding NH3 and (CH3)3N; addn. of concd. H2SO4; sepn. of HSO3NH2;; | 80% |
Conditions | Yield |
---|---|
With sodium carbonate In water byproducts: sodium sulfate; aq. soln. of NaNO2/Na2CO3; introduction of SO2 (until acidic/litmus); addn. of a drop concd. H2SO4; formation of N(SO3)(3-); hydrolysis; short heating or left for several hours (stream of air); neutralization (Na2CO3); evapn.; left (12h/0°C);; filtration from sodium sulfate; addn. of concd. H2SO4; immediate pptn. of most HSO3NH2 (left for another day/cooling); dried on clay; washed (ice cold water); recrystn. (hot water);; | 75% |
With Na2CO3 In water byproducts: sodium sulfate; aq. soln. of NaNO2/Na2CO3; introduction of SO2 (until acidic/litmus); addn. of a drop concd. H2SO4; formation of N(SO3)(3-); hydrolysis; short heating or left for several hours (stream of air); neutralization (Na2CO3); evapn.; left (12h/0°C);; filtration from sodium sulfate; addn. of concd. H2SO4; immediate pptn. of most HSO3NH2 (left for another day/cooling); dried on clay; washed (ice cold water); recrystn. (hot water);; | 75% |
Conditions | Yield |
---|---|
In neat (no solvent) byproducts: CO2; vigorous reaction (careful heating/cooling/stirring); temp. dependence on mechanism discussed;; | 73.4% |
In neat (no solvent) byproducts: CO2; vigorous reaction (careful heating/cooling/stirring); temp. dependence on mechanism discussed;; | 73.4% |
In not given equimolar amounts;; |
Conditions | Yield |
---|---|
In water aq. hydroxylammonium sulfate soln. cooled to -30°C; excess of SO2 condensed into vessel and left for 24 h in autoclave (at common temps.);; removal of SO2 (passing air through soln.); crystallization, filtration;washing (alc., ether); drying (air); further pptn. of HSO3NH2 by addn. of concd. H2SO4 to mother lye (at 0°C);; | 72% |
In water aq. medium; dependence of pressure (1.14-3.52 kg/cm*cm more than atm.) and temp. (5-30°C); formation of liquid SO2 should be avoided; pptn.;; | |
In water aq. medium; dependence of pressure (1.14-3.52 kg/cm*cm more than atm.) and temp. (5-30°C); formation of liquid SO2 should be avoided; pptn.;; |
Conditions | Yield |
---|---|
In water K2S2O7 (contaminated with 40% KHSO4) dild. in ammonia water (25%/shakingfor 0.5 h/cooling with cold water); until evolution of heat stops; heating (3 min/water bath);; left cooling; filtration, washing (ammonia water); evapn.; addn. of concd. H2SO4; left for several hours (common temps.); filtration; drying on clay; recrystn. from water;; | 60% |
Conditions | Yield |
---|---|
In water byproducts: dimethylaniline; diln. in ice cold ammonia water (10% NH3/) left warming up to common temps. under sepn. of (CH3)2NC6H5;; evapn. (removal of exceeding NH3 and (CH3)2NC6H5/water bath); addn. of concd. H2SO4; sepn. of HSO3NH2;; | 58% |
Conditions | Yield |
---|---|
In sulfuric acid heating a soln. of 1.1g pyridinium salt of carbamidosulfonic acid in 2.5 ml 100% H2SO4 at 110 °C for 0.5 h;; | 50% |
trisulfimide
A
sulfuric acid
B
aminosulfonic acid
C
SULFAMIDE
Conditions | Yield |
---|---|
With water in the cold, 48 h, 2 M HCl; | A 33% B n/a C n/a |
With H2O in the cold, 48 h, 2 M HCl; | A 33% B n/a C n/a |
In water decompn. in aq. soln.; 0 and 22°C discussed; presece of acid discussed;; |
Conditions | Yield |
---|---|
In water introduction of SO2 into aq. hydroxylammonium salt soln.;; | A 10% B n/a |
In water introduction of SO2 into aq. hydroxylammonium salt soln.;; | A 10% B n/a |
Conditions | Yield |
---|---|
at 25℃; unter Druck; |
Conditions | Yield |
---|---|
at 0℃; unter Druck; |
(N-acetyl-acetimidoyl)-amidosulfuric acid
water
A
N-acetylacetamide
B
aminosulfonic acid
Conditions | Yield |
---|---|
In sulfuric acid react. of SO3-vapor with urea, sulfatolysis;; | |
In sulfuric acid aq. H2SO4; react. of SO3-vapor with urea, sulfatolysis;; |
Conditions | Yield |
---|---|
With sulfuric acid In sulfuric acid at 80 - 90°C; |
Conditions | Yield |
---|---|
heating on water bath; equimolar amts. of educts; forming small amt. of triuret; |
nitromethane
sulfur trioxide
A
carbon dioxide
B
aminosulfonic acid
C
hydroxylamine-O-sulfonic acid
Conditions | Yield |
---|---|
above 0°C; |
sulfur dioxide
ammonia
A
S4N2
B
aminosulfonic acid
C
sulfur
D
tetrasulfur tetranitride
Conditions | Yield |
---|---|
With water In gas excess of SO2, 50-80°C, the solid product hydrolysed by water; |
Conditions | Yield |
---|---|
In thionyl chloride amidosulfuric acid placed into a flask and suspended in thionyl dichloride under dry N2; HSO3Cl added, then the flask fitted with a reflux condenser, connected to a CaCl2 drying tube; heated at 130°C for 24 h; reaction mixture fractionally distilled under vacuum; main fraction collected at 95°C/650 Pa; | 99% |
Hippuric Acid
aminosulfonic acid
4-chloro-3-(2,2,3,3,3-pentafluoropropoxymethyl)aniline
2-phenyl-4,5-oxazoledione 4-[4-chloro-3-(2,2,3,3,3,-pentafluoropropoxymethyl)-phenylhydrazone]
Conditions | Yield |
---|---|
With hydrogenchloride; sodium acetate; acetic anhydride; acetic acid; sodium nitrite In water | 98.1% |
Conditions | Yield |
---|---|
With chlorosulfonic acid at 130℃; for 24h; Inert atmosphere; | 98% |
Hippuric Acid
aminosulfonic acid
4-chloro-3-(2,2,3,3,3-pentafluoropropoxymethyl)aniline
Conditions | Yield |
---|---|
With hydrogenchloride; sodium acetate; acetic anhydride; acetic acid; sodium nitrite In water | 97.95% |
With hydrogenchloride; sodium acetate; acetic anhydride; acetic acid; sodium nitrite In water | 97.1% |
Conditions | Yield |
---|---|
With KOH In water calcd. amts. of educts; mixing cold aq. solns. of educts under stirring; product pptd. after 2-3 d; sucking off, washing with cold H2O, drying; | 97% |
Conditions | Yield |
---|---|
With NaOH In water calcd. amts. of educts; pptn. 3-4 d; washing with alc. and ether; drying in vac. over P2O5; | 97% |
With sodium hydroxide In water 1.5 fold molar excess of NaOH; amidosulfuric acid neutralized with NaOH soln.; adding hot aq. soln. of HgCl2; pptd. after 3-4 d; washing with H2O, alc. and ether; drying in vac.; | |
With NaOH In water 1.5 fold molar excess of NaOH; amidosulfuric acid neutralized with NaOH soln.; adding hot aq. soln. of HgCl2; pptd. after 3-4 d; washing with H2O, alc. and ether; drying in vac.; |
chlorosulfonic acid
thionyl chloride
aminosulfonic acid
bis(chlorosulfonyl)amine
Conditions | Yield |
---|---|
at 70 - 130℃; for 24h; | 96% |
at 130℃; Inert atmosphere; | Ca. 449 g |
2,3-difluoroanilline
aminosulfonic acid
acrylic acid
2,4-Difluorocinnamic acid
Conditions | Yield |
---|---|
With sulfuric acid; sodium nitrite; palladium diacetate In water | 95% |
sodium chlorite
4-iodo-α-methylbenzeneacetaldehyde
aminosulfonic acid
(RS)-2-(4'-iodophenyl)propanoic acid
Conditions | Yield |
---|---|
With sodium hydroxide In water; 1,2-dichloro-ethane | 94% |
sodium chlorite
4-iodo-α-methylbenzeneacetaldehyde
aminosulfonic acid
(RS)-2-(4'-iodophenyl)propanoic acid
Conditions | Yield |
---|---|
With sodium hydroxide; sodium hydrogen sulphite In water; 1,2-dichloro-ethane | 94% |
Conditions | Yield |
---|---|
With NaOH In water calcd. amts. of educts; adding aq. suspension of freshly prepared HgO into hot neutralized soln. of amidosulfuric acid; cooling, sucking off; washing with cold H2O; drying; | 94% |
With NaOH In water calcd. amts. of educts; adding boiling aq. soln. of neutralized amidosulfuric acid dropwise into aq. suspension of yellow HgO; product pptd. by cooling after 24 h; | 79% |
Conditions | Yield |
---|---|
With KOH In water calcd. amts. of educts; mixing cold aq. solns. of educts under stirring, heating, cooling; decanting with cold H2O; sucking off; product contains Cl; | 94% |
aminosulfonic acid
3β,7β-dihydroxy-5β-cholan-24-oic acid
Conditions | Yield |
---|---|
In DMF (N,N-dimethyl-formamide) at 45 - 90℃; for 0.5h; | 93.7% |
Conditions | Yield |
---|---|
With KOH In water adding amidosulfuric acid into aq. KOH soln.; this soln. adding to aq. suspension of freshly pptd. HgO; shaking for 1 h; filtrate storing for several h; sucking off the ppt.; washing with cold H2O, drying; | 92% |
With potassium hydroxide In not given calcd. amts. of educts; amidosulfuric acid neutralized with KOH soln., adding more KOH soln. and freshly prepared HgO; heating 1 h on water bath; product pptd. from filtrate at ambient temp.; sucking off; recrystn. from 0.5 % KOH soln.; washing with alc. and ether; drying in air; storage in vac. over P2O5; | |
With KOH In not given calcd. amts. of educts; amidosulfuric acid neutralized with KOH soln., adding more KOH soln. and freshly prepared HgO; heating 1 h on water bath; product pptd. from filtrate at ambient temp.; sucking off; recrystn. from 0.5 % KOH soln.; washing with alc. and ether; drying in air; storage in vac. over P2O5; |
sodium chlorite
aminosulfonic acid
2-(benzo[1,3]dioxol-5-yl)-4-chloro-6-isopropoxy-2H-chromene-3-carbaldehyde
2-(benzo[1,3]dioxol-5-yl)-4-chloro-6-isopropoxy-2H-chromene-3-carboxylic acid
Conditions | Yield |
---|---|
With sodium hydroxide; sodium sulfite In water; toluene | 91% |
aminosulfonic acid
2-Chloronitrobenzene
B
3-nitro-4-chlorosulfonyl chloride
Conditions | Yield |
---|---|
With chlorosulfonic acid | A n/a B 90.8% |
aminosulfonic acid
3-cyclopentyloxy-4-methoxybenzylaldehyde
3-cyclopentyloxy-4-methoxy benzoic acid
Conditions | Yield |
---|---|
With sodium chloride In water; acetic acid | 90% |
With sodium In water; acetic acid |
sodium chlorite
(1-phenyl-cyclopentyl)-acetaldehyde
aminosulfonic acid
(1-phenyl-cyclopentyl)-acetic acid
Conditions | Yield |
---|---|
In tert-butyl alcohol | 90% |
sodium hydroxide
aminosulfonic acid
hydrogen bromide
N-bromosulfamic acid sodium salt
Conditions | Yield |
---|---|
Stage #1: hydrogen bromide With dihydrogen peroxide In water at 61.1011℃; Stage #2: aminosulfonic acid In water at 34.99℃; Stage #3: sodium hydroxide With sode de l'acide trichloroisocyanurique Product distribution / selectivity; more than 3 stages; | 88.4% |
Stage #1: hydrogen bromide With dihydrogen peroxide In water at 61.1011℃; Stage #2: aminosulfonic acid In water at 29.4344 - 34.99℃; Stage #3: sodium hydroxide With trichloroisocyanuric acid Product distribution / selectivity; more than 3 stages; | 80.1% |
Stage #1: hydrogen bromide With dihydrogen peroxide In water at 61.1011℃; Stage #2: aminosulfonic acid In water at 34.99℃; Stage #3: sodium hydroxide With calcium hypochlorite Product distribution / selectivity; more than 3 stages; | 70.8% |
aminosulfonic acid
2-amino-5-methoxybenzenesulfonic acid
2-sulfo-4-methoxybenzoic acid
Conditions | Yield |
---|---|
With sulfuric acid; sodium nitrite; palladium(II) chloride In water; acetonitrile | 88% |
Conditions | Yield |
---|---|
In water | 86% |
aminosulfonic acid
potassium sulfamate
Conditions | Yield |
---|---|
With potassium hydroxide In water at 20℃; for 0.416667h; | 86% |
sodium hydroxide
aminosulfonic acid
sodium bromide
N-bromosulfamic acid sodium salt
Conditions | Yield |
---|---|
Stage #1: sodium hydroxide; aminosulfonic acid; sodium bromide In water at 26.6567 - 32.2122℃; pH=2; Stage #2: With trichloroisocyanuric acid In water for 0.25 - 0.5h; Product distribution / selectivity; | 85% |
Stage #1: aminosulfonic acid; sodium bromide In water at 26.6567 - 32.2122℃; pH=2; Stage #2: With calcium hypochlorite In water for 0.25 - 0.5h; Stage #3: sodium hydroxide In water at 26.6567 - 32.2122℃; Product distribution / selectivity; |
1-(2,6-dinitro-4-trifluoromethylphenyl)-2-chloro-3-cyano-4-dichlorofluoro-methylsulfenyl-5-methylpyrrole
aminosulfonic acid
2-chloro-3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-(dichlorofluoromethylsulfenyl)-5-methylpyrrole
Conditions | Yield |
---|---|
With lithium chloride In 1-methyl-pyrrolidin-2-one | 85% |
2-amino-6-(1-hydroxyethyl)-benzoic acid (sodium salt)
aminosulfonic acid
hydrogen sulfide
7-mercapto-3-methyl-3H-isobenzofuran-1-one
Conditions | Yield |
---|---|
With hydrogenchloride; sodium hydroxide; sodium hydrogen sulphite; acetic acid; triphenylphosphine In water; toluene | 85% |
Conditions | Yield |
---|---|
In water | 85% |
Conditions | Yield |
---|---|
With sulfuric acid; sodium nitrite; palladium diacetate In water | 84% |
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