Conditions | Yield |
---|---|
With sodium hydroxide |
citric acid monohydrate
Conditions | Yield |
---|---|
In methanol at 20℃; for 0.166667h; | 98.8% |
citric acid monohydrate
Conditions | Yield |
---|---|
In methanol at 20℃; for 0.166667h; | 97.8% |
Conditions | Yield |
---|---|
Stage #1: citric acid monohydrate With calcium oxide In water at 20℃; Stage #2: L-lysine In water at 70 - 80℃; for 4h; | 97.1% |
Conditions | Yield |
---|---|
Stage #1: citric acid monohydrate With calcium hydroxide In water at 20℃; Stage #2: L-arginine In water at 70 - 80℃; for 4h; | 96% |
Conditions | Yield |
---|---|
Stage #1: citric acid monohydrate With calcium carbonate In water at 20℃; Stage #2: Acetyl-L-carnitine In water at 70 - 80℃; for 4h; | 95.8% |
citric acid monohydrate
propionyl-L-carnitine
Conditions | Yield |
---|---|
Stage #1: citric acid monohydrate With calcium hydroxide In water at 20℃; Stage #2: propionyl-L-carnitine In water at 70 - 80℃; for 4h; | 95.3% |
ammonia
dihydrogen peroxide
titanium tetrachloride
citric acid monohydrate
zinc(II) carbonate
Conditions | Yield |
---|---|
In water TiCl4 added dropwise to a water on ice bath, H2O2 and acid added, allowed to warm to room temp., carbonate added, pH adjusted to 2 (aq. ammonia); crystd. (THF/water) for several d at 4°C; elem. anal.; | 94.6% |
water
titanium tetrachloride
citric acid monohydrate
lithium hydroxide
Conditions | Yield |
---|---|
In water TiCl4 added dropwise to a water on ice bath, acid added at room temp., pH adjusted to 2 (LiOH); stored for several d at room temp.; elem. anal.; | 93.7% |
citric acid monohydrate
Conditions | Yield |
---|---|
In ethyl acetate at 70℃; for 2h; | 89.5% |
ammonia
dihydrogen peroxide
titanium tetrachloride
citric acid monohydrate
Conditions | Yield |
---|---|
In water addn. of titanium chloride to water at 0°C, addn. of hydrogen peroxide and citric acid, warming to room temp., addn. of gold compd., adjusting pH to 2 by aq. ammonia; crystn. at 4°C from aq. THF, elem. anal.; | 89% |
Conditions | Yield |
---|---|
In water byproducts: H2O; dissolving of Al(NO3)3*9H2O and citric acid monohydrate with 1:2 molar ratio in nano-pure water; stirring at 50°C overnight, rotary evapn. to dryness, redissolving in min. amt. of H2O, adjusting of pH to 4.5 with aq. ammonia; crystn. at 4°C in abs. ethanol, filtration; elem. anal.; | 88.4% |
ammonia
dihydrogen peroxide
titanium tetrachloride
citric acid monohydrate
caesium carbonate
Conditions | Yield |
---|---|
In water TiCl4 added dropwise to H2O, cooled in an ice bath, H2O2 soln. and citric acid monohydrate added, warmed to room temp., treated with Cs2CO3, pH adjusted to 2 using NH3 soln.; crystd. from H2O/THF at 4°C for days; elem. anal.; | 87.4% |
ammonia
dihydrogen peroxide
titanium tetrachloride
lithium carbonate
citric acid monohydrate
Conditions | Yield |
---|---|
In water TiCl4 added dropwise to a water on ice bath, H2O2 and acid added, allowed to warm to room temp., carbonate added, pH adjusted to 2 (aq. ammonia); crystd. (THF/water) for several d at 4°C; elem. anal.; | 86.4% |
water
citric acid monohydrate
[La(citric acis(-3H))(H2O)]
Conditions | Yield |
---|---|
In water High Pressure; under hydrothermal conditions; equimolar mixt. of La2O3 and citric acid in water (pH 2.2-2.5) heated at 120°C for 5 d; ppt. sepd. from hot mixt.; washed with cold water; dried under vac.; elem. anal.; | 85% |
citric acid monohydrate
p-nitrobenzyl (4R,5S,6S)-3-<(3S,5S)-5-dimethylaminocarbonyl-1-(p-nitrobenzyloxycarbonyl)pyrrolidin-3-ylthio>-4-methyl-7-oxo-6-<(1R)-1-trimethylsilyloxoethyl>-1-azabicyclo<3.2.0>hept-2-en-2-carboxylate
p-nitrobenzyl (4R,5S,6S)-3-<(3S,5S)-5-dimethylaminocarbonyl-1-(p-nitrobenzyloxycarbonyl)pyrrolidin-3-ylthio>-6-<(1R)-1-hydroxyethyl>-4-methyl-7-oxo-1-azabicyclo<3.2.0>hept-2-en-2-carboxylate
Conditions | Yield |
---|---|
In methanol | 84% |
In methanol | 84% |
Conditions | Yield |
---|---|
In water High Pressure; under aerobic conditions; citric acid hydrate (2 mmol) and MnCO3 (1 mmol) dissolved in H2O, mixt. heated at 160°C in sealed teflon tube for 3 d; elem. anal.; | 84% |
With Ca(NO3)2 In water High Pressure; under aerobic conditions; citric acid hydrate, Ca(NO3)2, and MnCO3 (molar ratio = 8:1:4-5) dissolved in H2O, mixt. heated at 160°C in sealed teflon tube for 3 d; elem. anal.; |
ethanol
silver(I) citrate
citric acid monohydrate
triphenylphosphine
[(Ph3P)2Ag(H2cit)]*EtOH
Conditions | Yield |
---|---|
In ethanol mixt. Ag3cit, citric acid monohydrate, PPh3 and EtOH was heated with stirring; soln. was filtered hot and allowed to cool slowly, ppt. was colledcted and washed with ice-cold EtOH; elem. anal.; | 84% |
citric acid monohydrate
Conditions | Yield |
---|---|
In ethyl acetate at 70℃; for 1.5h; | 83.1% |
citric acid monohydrate
Conditions | Yield |
---|---|
In ethyl acetate at 70℃; for 1.5h; | 82% |
Conditions | Yield |
---|---|
With KOH In ethanol; water V2O5 dissolved in KOH soln., mixed with an aq. soln. of citric acid monohydrate, 1,10-phenanthroline monohydrate in EtOH added, brought to pH 4.0 with a KOH soln.; crystd. for 2 wk, sepd., washed with EtOH; elem. anal.; | 81% |
citric acid monohydrate
2,2-difluoroethyl triflate
1-(2,2-difluoroethyl)-7-methyl-2-oxo-1,2,3,4-tetrahydroquinoline-6-carboxylic acid ethyl ester
Conditions | Yield |
---|---|
With sodium hydride In N,N-dimethyl-formamide | 81% |
[(1R)-1-{2-[(2,5-difluorophenyl)formamido]acetamido}-3-methylbutyl]boronic acid
citric acid monohydrate
Conditions | Yield |
---|---|
In ethyl acetate at 70℃; for 2h; | 80.5% |
Conditions | Yield |
---|---|
In water aq. KOH was added to an aq. soln. to pH about 2; recrystd. from hot water; elem. anal.; | 80% |
Conditions | Yield |
---|---|
In water pH of aq. soln. of TiCl4 and citric acid monohydrate adjusted to 2.0 by addn. aq. ammonia, stirred for 30 min; ppt. collected and recrystd. from hot water; elem. anal.; | 80% |
Conditions | Yield |
---|---|
In water ZnO (5 mmol) added to aq. soln. of TiCl4 (10 mmol) and citric acid monohydrate (30 mmol); pH adjusted to 2.0 by addn. of NH4OH; elem. anal.; | 80% |
Conditions | Yield |
---|---|
In water Fe (5 mmol) added to aq. soln. of TiCl4 (10 mmol) and citric acid monohydrate (30 mmol); pH adjusted to 2.0 by addn. of NH4OH; elem. anal.; | 80% |
citric acid monohydrate
Conditions | Yield |
---|---|
In ethyl acetate at 70℃; for 0.5h; | 80% |
Conditions | Yield |
---|---|
Stage #1: (5-((2,5-difluorobenzyl)oxy)-1-(3,3-dimethylbutyl)-1H-pyrazol-3-yl)methylmethanesulfonate; methylamine In methanol; toluene at 5℃; for 1.25h; Stage #2: citric acid monohydrate In isopropyl alcohol | 76.3% |
manganese (II) acetate tetrahydrate
tripotassium citrate monohydrate
citric acid monohydrate
KMn(citrate)(H2O)
Conditions | Yield |
---|---|
In ethanol; water High Pressure; 2 equiv. of Mn-salt, 1.5 equiv. of K-citrate and 1.0 equiv. of citric acid were heated in alcohol/H2O at 160 °C for 3 d in a teflon-linedstainless steel autoclave; cooling, crystals were air-dried, elem. anal.; | 76% |
citric acid monohydrate
Conditions | Yield |
---|---|
With ammonium hydroxide In water a soln. of Ce-complex and citric acid in water was stirred for 0.5 h, pHwas adjusted to 5.5 by 5% NH4OH, heated at 70°C for 2 days; evapd., washed with cold water and ethanol, dried in air; elem. anal.; | 76% |
The Citric acid monohydrate, with the CAS registry number 5949-29-1, is also known as cis-Permethric acid; cis-(Dichlorovinyl)dimethylcyclopropanecarboxylic acid; cis-DL-3-(2,2-Dichlorovinyl)-2,2-dimethylcyclopropanecarboxylic acid. It belongs to the product categories of Organic matters.This chemical's molecular formula is C6H8O7.H2O and molecular weight is 210.14.What's more,Its systematic name is Citric acid monohydrate. It is white crystals or powder,Stable.Incompatible with oxidizing agents, bases, reducing agents, nitrates.
Physical properties about CIS-Cypermethric Acid are:(1)ACD/LogP: -1.721; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): -6.53; (4)ACD/LogD (pH 7.4): -7.46; (5)ACD/BCF (pH 5.5): 1.00; (6)ACD/BCF (pH 7.4): 1.00; (7)ACD/KOC (pH 5.5): 1.00; (8)ACD/KOC (pH 7.4): 1.00; (9)#H bond acceptors: 7; (10)#H bond donors: 4; (11)#Freely Rotating Bonds: 6; (12)Flash Point: 155.2 °C; (13)Enthalpy of Vaporization: 63.82 kJ/mol ; (14)Boiling Point: 309.6 °C at 760 mmHg; (15)Vapour Pressure: 5.73E-05 mmHg at 25°C;
The Citric acid monohydrate is highly Flammable,risk of serious damage to eyes. It is Irritating to eyes, respiratory system and skin. Its Vapors may cause drowsiness and dizziness.When you use it, wear suitable protective clothing, gloves and eye/face protection,Keep away from sources of ignition - No smoking .In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.Keep container in a well-ventilated place.
You can still convert the following datas into molecular structure:
(1)SMILES:O=C(O)CC(O)(C(=O)O)CC(=O)O.O;
(2)Std. InChI:InChI=1S/C6H8O7.H2O/c7-3(8)1-6(13,5(11)12)2-4(9)10;/h13H,1-2H2,(H,7,8)(H,9,10)(H,11,12);1H2;
(3)Std. InChIKey:YASYEJJMZJALEJ-UHFFFAOYSA-N.
The toxicity data of Citric acid monohydrate as follows:
Organism | Test Type | Route | Reported Dose (Normalized Dose) | Effect | Source |
---|---|---|---|---|---|
rat | LD50 | intraperitoneal | 375mg/kg (375mg/kg) | National Technical Information Service. Vol. AD-A121-876, |
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