Conditions | Yield |
---|---|
In water concentration of aq. soln. at 55°C, 8.6 Torr; pptn.; temp. must be >47°C;; centrifuging;; | |
In water concentration of aq. soln. at 55°C, 8.6 Torr; pptn.; temp. must be >47°C;; centrifuging;; |
citric acid ; trisodium-salt pentahydrate
A
water
B
trisodium citrate dihydrate
Conditions | Yield |
---|---|
In neat (no solvent) heating at temp. above 145°C;; | |
In neat (no solvent) heating at temp. above 145°C;; |
trisodium citrate dihydrate
Conditions | Yield |
---|---|
In water crystn. from Na2HC6H5O7 soln. under ethanol at 23°C;; |
trisodium citrate dihydrate
Conditions | Yield |
---|---|
In neat (no solvent) byproducts: H2O; dehydration at 100°C;; | |
In neat (no solvent) byproducts: H2O; dehydration at 100°C;; |
Conditions | Yield |
---|---|
In neat (no solvent) heating at temp. above 145°C;; | |
In neat (no solvent) heating at temp. above 145°C;; |
cis-α-dichloro(triethylenetetramine)cobalt(III) chloride
trisodium citrate dihydrate
β-[(citrato)(triethylenetetramine)cobalt(III)] pentahydrate
Conditions | Yield |
---|---|
With (C2H5)3N; H2O In methanol ligand salt, complex and (C2H5)3N refluxed for 40 h in MeOH; evapd. (vac.), solids dissolved in H2O, chromd. (cation-exchange, H(1+)-form, aq. NH3), evapd. (vac.), recrystd. (H2O/MeOH) at 70°C, dried at 100°C overnight; elem. anal.; | 55.4% |
cis,trans-2,5-dimethoxytetrahydrofuran
acetonedicarboxylic acid
ethylamine
trisodium citrate dihydrate
N-ethylnortropinone
Conditions | Yield |
---|---|
With hydrogenchloride In water | 46% |
acetonedicarboxylic acid
trisodium citrate dihydrate
benzylamine
N-benzyltropinone
Conditions | Yield |
---|---|
With hydrogenchloride In water | 44% |
isopropylamine
trisodium citrate dihydrate
8-aza-8-isopropyl-bicyclo<3.2.1>octan-3-one
Conditions | Yield |
---|---|
With hydrogenchloride In water | 40% |
acetonedicarboxylic acid
trisodium citrate dihydrate
Cyclopropylamine
8-cyclopropyl-8-azabicyclo-[3.2.1]-octan-3-one
Conditions | Yield |
---|---|
With hydrogenchloride In water | 33% |
Conditions | Yield |
---|---|
With NaOH; air In water a soln. of sodium citrate dihydrate added to TiCl3 under N2, air-oxidized, pH increased to 7 using NaOH; crystd. by diffusion of MeOH into the soln. at 4°C; elem. anal.; | 22.5% |
trisodium citrate dihydrate
Conditions | Yield |
---|---|
With quinoline In water Al(NO3)3*9H2O, Na3C6H5O7*2H2O (1:1 or 10:1 Al to citrate ratios) dissolved in H2O; quinoline added dropwise with const. stirring; soln. stirred for 30 min (optimum pH 1.660, but complex also formed in the pH range 1.2 to 3.0); crystals formed after 48 h; elem. anal.; | 22% |
trisodium citrate dihydrate
Conditions | Yield |
---|---|
In water byproducts: neocuproinium nitrate; equimolar amts., stirring at 60°C for 30 min; standing at room temp. for 24 h, filtration off of neocuproininum nitrate, crystn. at 27°C (several d); | 15% |
1,4,8,11-tetra(4-pyridylmethyl)-1,4,8,11-tetraazacyclotetradecane
water
trisodium citrate dihydrate
Conditions | Yield |
---|---|
In water High Pressure; Cd:citate:amine=0.14:0.071:0.071 molar ratio, heated at 110°C for3 d; mechanical separated; elem. anal.; | 12% |
1-(1-phenylcyclohexyl)-4-hydroxypiperidine
sulfuric acid
mercury (II) chloride
trisodium citrate dihydrate
isopropyl alcohol
1-(1-phenylcyclohexyl)-4-piperidone
Conditions | Yield |
---|---|
With hydrogenchloride In methanol; chloroform; water; acetic acid |
1-(1-phenylcyclohexyl)-4-hydroxypiperidine
mercury (II) chloride
trisodium citrate dihydrate
isopropyl alcohol
1-(1-phenylcyclohexyl)-4-piperidone
Conditions | Yield |
---|---|
With hydrogenchloride; sulfuric acid In methanol; chloroform; water; acetic acid |
trisodium citrate dihydrate
Conditions | Yield |
---|---|
In water soln. of HAuCl4 added 1% citrate within period of 5 s while refluxing with vigorous stirring under N2 atm.; Au soln. kept refluxing for period of 1 h and then left to cool to room temp.; detd. by absorption spect.; |
trisodium citrate dihydrate
Conditions | Yield |
---|---|
In water |
trisodium citrate dihydrate
Conditions | Yield |
---|---|
In water dissoln. in H2O; crystn. at ambient temp.;; | |
In water dissoln. in H2O; crystn. at ambient temp.;; |
Conditions | Yield |
---|---|
In water sodium citrate soln. in water added dropwise into the silver nitrate soln. in water; centrifugation, washed with distilled water, absolute alcohol in sequence and dried in air; |
trisodium citrate dihydrate
Conditions | Yield |
---|---|
With sodium carbonate In water mixing of solns. of equimolar amts. of salts, adjusting pH to 5.5 with Na2CO3, refluxed; pptn. with methanol, washing with 80% methanol-water, drying in vac.; elem. anal.; |
Conditions | Yield |
---|---|
With Na3H2MoO4(C6H5O7) In water soln. of Na2MoO4 and Na3C6H5O7 mixed in various proportions, pH adjusted by H2SO4 to 5.00; |
trisodium citrate dihydrate
Conditions | Yield |
---|---|
In water aq. soln. of sodium citrate and 0.1 wt.-% of CuSO4*5H2O slowly evapd. for a few days; |
trisodium citrate dihydrate
Conditions | Yield |
---|---|
In water VOSO4*3H2O (0.01 mol%) mixed with aq. soln. of sodium citrate; crystd. by slow evapn. of satd. soln.; single crystals obtained; |
trisodium citrate dihydrate
Conditions | Yield |
---|---|
With citric acid; polyethylene glycol 400; NH3 In water sol-gel method: salts dissolved in aq. citric acid, polyethylene glycol 400 added, NH3 added to adjust pH to 1.0-2.0, mixt. stirred, heated to m80 °C for 24 h, dried at 120 °C for 12 h, xerogel cacined (750 °C, 4 h, air); detd. by XRD; |
trisodium citrate dihydrate
Conditions | Yield |
---|---|
With citric acid; polyethylene glycol 400; NH3 In water sol-gel method: salts dissolved in aq. citric acid, polyethylene glycol 400 added, NH3 added to adjust pH to 1.0-2.0, mixt. stirred, heated to m80 °C for 24 h, dried at 120 °C for 12 h, xerogel cacined (750 °C, 4 h, air); detd. by XRD; |
Conditions | Yield |
---|---|
With aq. NH3 In water High Pressure; Mn salt and citrate were added to H2O under stirring; aq. NH3 added at room temp. soln. stirred for several min; transferred in Teflon lined stainless steel autoclave; sealed; heated at 160°C for 2 h; collected; washed; dried in vac.; |
Conditions | Yield |
---|---|
at 95℃; for 12h; Temperature; Time; Autoclave; |
1. Introduction of Trisodium citrate dihydrate
Trisodium citrate dihydrate is also called citric acid trisodium salt dehydrate, it is the sodium salt of citric acid combined with 2 water molecules. The IUPAC name of Trisodium citrate dihydrate is trisodium 2-hydroxypropane-1,2,3-tricarboxylate dehydrate. It is white powder or colourless crystals,odorless and salty cool. And the product categories are inorganic & organic chemicals;food additives;food and feed additive.
2. Properties of Trisodium citrate dihydrate
Nominal Mass: 294 Da
Average Mass: 294.0996 Da
Monoisotopic Mass: 293.993967 Da
Flash Point: 155.2 °C
Enthalpy of Vaporization: 63.82 kJ/mol
Boiling Point: 309.6 °C at 760 mmHg
Storage temp: Store at RT.
Water Solubility: 720 g/L (25 ºC)
Merck: 14,8602
BRN: 6104939
Stability: Stable. Incompatible with bases, reducing agents, oxidizing agents.
Vapour Pressure: 5.73E-05 mmHg at 25°C
3. Structure Descriptors of Trisodium citrate dihydrate
InChI=1/C6H8O7.3Na.2H2O/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);;;;2*1H2/q;3*+1;;/p-3
Smiles
O=C([O-])CC(C([O-])=O)(O)CC([O-])=O.[Na+].[Na+].[Na+].O.O
Classification Code: Alkalizer [systemic]
4. Safety Information of Trisodium citrate dihydrate
Hazard Codes: Xi
Risk Statements: 37/38-41-36/37/38
R37/38: Irritating to respiratory system and skin
R41: Risk of serious damage to the eyes
R36/37/38: Irritating to eyes, respiratory system and skin
Safety Statements: 26-36/37/39-24/25-36
S26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice
S36/37/39: Wear suitable protective clothing, gloves and eye/face protection
S24/25: Avoid contact with skin and eyes
S36: Wear suitable protective clothing
WGK Germany: 1
RTECS: GE7810000
5. Use of Trisodium citrate dihydrate
Trisodium citrate dihydrate has a sour taste similar to citric acid, and is salty as well. It is often used as a food preservative, and as a flavoring in the food industry. In the pharmaceutical industry it is used to control pH. And trisodium citrate dihydrate may be used as an alkalizing agent, buffering agent, emulsifier, or sequestering agent. What’s more, it is used in nonhydrogen electroplation as well as widely in tail gas absorption process of sulfur dioxide for chemical and metallurgy industries. Its absorptivity reaches 99%. The waste absorbed may be regenerated into sulfur dioxide liquid and potassium citrate for cyclic utilization. The daily-use chemical detergent with potassium citrate. As raw material instead of sodium phosphate trimer, it is non-toxic and non-pollution.
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