B
magnesium chloride
Conditions | Yield |
---|---|
In tetrahydrofuran Ar atm.; hot THF; | A 100% B 100% |
Conditions | Yield |
---|---|
In melt melting the starting materials in an evacuated silica ampoule at 900°C for 48 h, cracking the ampoule under Ar; | 95% |
In neat (no solvent) reduction of molten ZnCl2 with Mg forming MgCl2;; | |
In neat (no solvent) reduction of molten ZnCl2 with Mg forming MgCl2;; |
zirconium(IV) chloride
magnesium
A
zirconium
B
magnesium chloride
Conditions | Yield |
---|---|
In melt heating at 800°C under inert gas in a closed vessel, Kroll-process; apparatus described;; separation of Mg and MgCl2 by vacuum destillation;; | A 93% B n/a |
In melt heating at 800°C under inert gas in a closed vessel, Kroll-process; apparatus described;; separation of Mg and MgCl2 by vacuum destillation;; | A 93% B n/a |
Conditions | Yield |
---|---|
In neat (no solvent) High Pressure; mixed, sealed in autoclave under Ar, heated at 450, 500, 550, and 600 °C for 10 h; washed with water, dried in vac. at 70 °C for 12 h; powder XRD; | A 93% B n/a C n/a D n/a |
dichlorobis(3,5-di-tert-butylpyrazolylato)titanium(IV)
methylmagnesium chloride
A
dimethylbis(3,5-di-tert-butylpyrazolylato)titanium(IV)
B
magnesium chloride
Conditions | Yield |
---|---|
In tetrahydrofuran; hexane Ar-atmosphere; MeMgCl soln. (THF) addn. (0°C), stirring (room temp., 20 h), evapn. (reduced pressure); extg. (hexane), filtering, evapn. (reduced pressure); elem. anal.; | A 93% B n/a |
(trimethylsilyl)methylmagnesium chloride
tantalum pentachloride
trimethylphosphane
B
magnesium chloride
Conditions | Yield |
---|---|
In diethyl ether; hexane under N2 atm. slurry TaCl5 in hexane at -20°C was treated dropwise with Me3SiCH2MgCl in Et2O, solvent was removed in vacuo, residue was taken up in hexane at 0°C and filtered, PMe3 was added and heated to 50°C for 1 h; soln. was filtered, concd. and cooled to -20°C; | A 92% B n/a |
rac-ethanediyl-bis(1-indenyl)zirconium dichloride
methylmagnesium bromide
B
magnesium chloride
Conditions | Yield |
---|---|
In 1,4-dioxane; diethyl ether; hexane (N2); dioxane was added to 3 M soln. MeMgBr in hexane and Et2O, stirred for 1 h, filtered, filtrate was added to soln. of zirconium complex in Et2O at -78°C, warmed to room temp. overnight; evapd., dissolved in benzene, filtered, evapd. in vac., crystd. from toluene/hexanes; | A 91% B n/a |
ethylmagnesium bromide
A
ethane
B
ethene
C
palladium
E
magnesium chloride
Conditions | Yield |
---|---|
In tetrahydrofuran To a soln. of anhydrous salt is added C2H5MgBr at 20°C with stirring. The reaction mixture is left for 5 - 6 h at room temp.; decantation, washing with THF, water and ethanol; electron diffraction; | A n/a B n/a C 90% D n/a E n/a |
bis(η5-tetramethyl(trimethylsilyl)cyclopentadienyl)titanium dichloride
magnesium
Bis(trimethylsilyl)ethyne
A
(η2-bis(trimethylsilyl)ethyne)bis(η5-tetramethyl(trimethylsilyl)cyclopentadienyl)titanium(II)
B
magnesium chloride
Conditions | Yield |
---|---|
In tetrahydrofuran -18°C (40 h), filtering, evapn. (vac.); extg. (hexane), MgCl2 pptn. (-5°C, overnight), concg., crystn. (-18°C, overnight); elem. anal.; | A 80% B n/a |
gallium
magnesium
methyl iodide
A
magnesium chloride
B
trimethyl gallium
Conditions | Yield |
---|---|
In neat (no solvent) inert gas atmosphere; mixing, heating in autoclave (100 - 160°C, stirring, 12 h); distillation; | A n/a B 65% |
gallium
magnesium
ethyl iodide
A
triethyl gallium
B
magnesium chloride
Conditions | Yield |
---|---|
In hexane inert condition; addn. of hexane to mixt. of Mg and Ga (vac.), addn. of hexane, dropwise addn. of EtI (boiling hexane); distillation; | A 65% B n/a |
gallium
iodine
magnesium
ethyl iodide
A
triethyl gallium
B
magnesium chloride
Conditions | Yield |
---|---|
In neat (no solvent) inert condition; addn. of I2 to mixt. of Mg and Ga, heating in vac. (150°C), chilling, addn. of EtI (50 - 70°C, 1 h), heating (90 °C, 4 h); distillation; | A 61% B n/a |
[ZrCl2(C32H38N4)]
dibenzylmagnesium
A
C39H45N4Zr(C4H8O)(CH2C6H5)
B
magnesium chloride
Conditions | Yield |
---|---|
In tetrahydrofuran; toluene stirring (room temp., 1 h); evapn., toluene addn., filtering, evapn., n-pentane addn., filtering, drying (vac.); elem. anal.; | A 61% B n/a |
Conditions | Yield |
---|---|
In neat (no solvent) inert condition; addn. of I2 to alloy Mg-Ga, heating in vac. (150 °C), chilling, addn. of EtI), heating (85°C, 4 h); distillation; | A 57% B n/a |
dimethylbis(3,5-di-tert-butylpyrazolylato)titanium(IV)
tert-butylamine
A
chlorotris(3,5-di-tert-butylpyrazolato)titanium(IV)
B
(tert-butylimido(chloro)(3,5-di-tert-butylpyrazolato)titanium)2
C
magnesium chloride
Conditions | Yield |
---|---|
In hexane byproducts: tert-butylammonium chloride; Ar-atmosphere; stirring (room temp., 16 h); filtering, evapn. (reduced pressure), crystn. (hexane, -15°C, -20°C); elem. anal.; | A 56% B 10% C n/a |
chlorotris(3,5-di-tert-butylpyrazolato)titanium(IV)
methylmagnesium chloride
A
methyltris(3,5-di-tert-butylpyrazolylato)titanium(IV)
B
magnesium chloride
Conditions | Yield |
---|---|
In tetrahydrofuran Ar-atmosphere; MeMgCl soln. (THF) addn. (0°C), stirring (room temp., 20 h), evapn. (reduced pressure); extg. (hexane), filtering, evapn. (reduced pressure); elem. anal.; | A 52% B n/a |
Conditions | Yield |
---|---|
With water In neat (no solvent) reduction of dry CaCl2 in H2-atmosphere on calcination with Mg; treatment of the reaction-products with H2O under formation of H2;; | A 50% B n/a C n/a |
With water In neat (no solvent) reduction of dry CaCl2 in H2-atmosphere on calcination with Mg; treatment of the reaction-products with H2O under formation of H2;; | A 50% B n/a C n/a |
With water In neat (no solvent) reduction of dry CaCl2 in CO2-atmosphere on calcination with Mg; treatment of the reaction-products with H2O under formation of H2;; | A 30% B n/a C n/a |
With water In neat (no solvent) reduction of dry CaCl2 in CO2-atmosphere on calcination with Mg; treatment of the reaction-products with H2O under formation of H2;; | A 30% B n/a C n/a |
Conditions | Yield |
---|---|
In diethyl ether under Ar, -80°C, molar ratio arsacarbollyl:(CH3)2CHMgCl=4.50:4.44, 1h stirring at room temp.; colorless ppt. is filtered off, solvent removed, extd. with hot hexane, evapd. to dryness, subl. in high vac. at 50°C, elem. anal.; | A 50% B n/a |
Vanadium (III) chloride-(tris-tetrahydrofuran)
pentafluorophenylmagnesium chloride
B
Tetrakis(pyridin)-dichlorovanadin(II)
C
magnesium chloride
Conditions | Yield |
---|---|
In tetrahydrofuran 1 mol of complex was slowly added to an THF soln. of 2 mol RMgCl at -15°C, after 1 h the temp. was raised to room temp. (Ar atm.);; dioxane in Et2O was added, evapd., ppt. was washed with Et2O;; | A 43% B 47% C n/a |
Vanadium (III) chloride-(tris-tetrahydrofuran)
(trimethylsilyl)methylmagnesium chloride
A
Tetrakis(pyridin)-dichlorovanadin(II)
B
tetrakis(trimethylsilylmethyl)vanadium
C
magnesium chloride
Conditions | Yield |
---|---|
In diethyl ether 1 mol of complex was slowly added to an ether soln. of 2 mol RMgCl at -15°C, after 1 h the temp. was raised to room temp. (Ar atm.);; dioxane was added, ppt. was extd. with pentane; elem. anal.;; | A 43% B 45% C n/a |
dichlorobis(3,5-di-tert-butylpyrazolylato)titanium(IV)
benzylmagnesium chloride
A
dibenzylbis(3,5-di-tert-butylpyrazolylato)titanium(IV)
B
magnesium chloride
Conditions | Yield |
---|---|
In diethyl ether; toluene Ar-atmosphere; BnMgCl soln. (Et2O) addn. (0°C), stirring (room temp., 16 h), evapn. (reduced pressure); extg. (hexane), filtering, concg. (reduced pressure), crystn. (-20°C, 2 d); elem. anal.; | A 43% B n/a |
trichloro-(3,5-di-tert-butylpyrazolylato)titanium(IV)
methylmagnesium chloride
A
dimethylbis(3,5-di-tert-butylpyrazolylato)titanium(IV)
B
magnesium chloride
Conditions | Yield |
---|---|
In tetrahydrofuran; hexane Ar-atmosphere; pptn. on mixing reagents (-78°C, 0.25 h), stirring(room temp., 3 h), evapn. (reduced pressure); extg. (hexane), filtering, evapn. (reduced pressure); | A 35% B n/a |
boron trifluoride
boron trichloride
B
boron nitride
C
magnesium chloride
Conditions | Yield |
---|---|
700-1000°C; diluterd with N2; washing with HCl at 1000°C; | A n/a B 34% C n/a |
Conditions | Yield |
---|---|
In diethyl ether under Ar, -80°C, molar ratio ClP((CH3)2C2B9H9):(CH3)2CHMgCl=1:1, warmed to -20°C; colorless ppt. is filtered off, solvent removed, extd. with hot hexane, evapd. to dryness, subl. in high vac. at room temp., elem. anal.; | A 33% B n/a |
magnesium chloride
Conditions | Yield |
---|---|
With hydrogenchloride In neat (no solvent) heating of brucite at 383-412 °C in a stream of dry HCl with formation of MgCl2; | 10.33% |
With HCl In neat (no solvent) heating of brucite at 383-412 °C in a stream of dry HCl with formation of MgCl2; | 10.33% |
Conditions | Yield |
---|---|
In butyldiglyme; ethyldiglym at 40℃; for 3h; |
isopropylmagnesium chloride
methyltrichlorogermane
B
magnesium chloride
Conditions | Yield |
---|---|
In butyldiglyme; ethyldiglym at 40℃; for 3h; |
isopropylmagnesium chloride
methyltrichlorogermane
B
magnesium chloride
Conditions | Yield |
---|---|
In butyldiglyme; ethyldiglym at 40℃; for 3h; |
Conditions | Yield |
---|---|
In butyldiglyme; ethyldiglym for 1h; |
triethylaluminum
n-butyl-ethylmagnesium
A
hydridomagnesium chloride
C
butyl magnesium bromide
D
ethylmagnesium chloride
E
magnesium chloride
Conditions | Yield |
---|---|
In 2-Methylpentane for 4383h; Reactivity; |
Conditions | Yield |
---|---|
With copper In glycerol byproducts: CuCl; Electrolysis; electrolysis of MgCl2 in anhydrous glycerin, copper electrodes, formation of CuCl at the anode and of C3H6O3Mg at the cathode;; | 100% |
With Cu In glycerol byproducts: CuCl; Electrolysis; electrolysis of MgCl2 in anhydrous glycerin, copper electrodes, formation of CuCl at the anode and of C3H6O3Mg at the cathode;; | 100% |
Conditions | Yield |
---|---|
In tetrachloromethane stirred vigorously for 3 d under N2; filtd. or evapn. of solvent under reduced pressure; | 99% |
magnesium chloride
MgCl(Zr2(OC3H7)9)
Conditions | Yield |
---|---|
In isopropyl alcohol; benzene byproducts: KCl; reflux (2 h), volatiles removal, stirring (70°C, 10 h), KCl pptn.; filtration, volatiles removal (27°C, red. pressure), pptn., recrystn. (n-hexane/toluene) or volatilization (210°C, 0.01 mmHg); elem. anal.; | 99% |
magnesium chloride
Mg(Zr2(OC3H7)9)2
Conditions | Yield |
---|---|
In isopropyl alcohol; benzene byproducts: KCl; reflux (2 h), volatiles removal, stirring (70°C, 10 h), KCl pptn., filtration, volatiles removal, (27°C, red. pressure), pptn.; volatilization (175°C, 0.1 mmHg) (70%); elem. anal.; | 99% |
aluminum isopropoxide
magnesium chloride
Mg(2+)*Cl(1-)*Al(OC3H7)4(1-)=MgCl(Al(OC3H7)4)
Conditions | Yield |
---|---|
In isopropyl alcohol; benzene byproducts: KCl; stirring (27°C, 12 h), pptn. (KCl), filtration; volatiles removal (reduced pressure, 27°C), recrystn. (hexane/toluene, -10°C); elem. anal.; | 99% |
Conditions | Yield |
---|---|
In diethyl ether under Ar atm. soln. Mg(BH4)2 in Et2O was prepared by react. MgCl2 and NaBH4 (V.N.Konoplev, Zh.Neorg.Khim., 1980, 25 (7), 1737-1740), anhydrous ammonia was passed through soln. at -10°C; react. mixt. was allowed to warm to room temp., volatiles were removed in vacuo; elem. anal.; | 99% |
Conditions | Yield |
---|---|
In tetrahydrofuran at 20℃; for 1h; Reagent/catalyst; Inert atmosphere; Schlenk technique; | 99% |
Conditions | Yield |
---|---|
With pyrographite In neat (no solvent) byproducts: MgO; heating of a mixture of SnO2 with double excess of MgCl2 forms 98.3 % SnCl4 at 800°C in presence of C;; | 98.3% |
In neat (no solvent) byproducts: MgO; heating of a mixture of SnO2 with double excess of MgCl2 forms 74.60 % SnCl4 at 800°C;; | 74.6% |
In neat (no solvent) byproducts: MgO; heating of a mixture of SnO2 with double excess of MgCl2 forms 58.79 % SnCl4 at 700°C; equilibrium reaction examinated;; | 58.79% |
Conditions | Yield |
---|---|
With pyrographite In neat (no solvent) byproducts: MgO, CO; formation at reaction of SnO2, MgCl2 and C under exclusion of air for 2 h at 800°C;; collecting of formed SnCl2 at 300-330°C in a condensator at exclusion of air;; | 98.3% |
With C In neat (no solvent) byproducts: MgO, CO; formation at reaction of SnO2, MgCl2 and C under exclusion of air for 2 h at 800°C;; collecting of formed SnCl2 at 300-330°C in a condensator at exclusion of air;; | 98.3% |
With pyrographite In neat (no solvent) byproducts: MgO, CO; heating of a mixture of SnO2 with double excess of MgCl2 in presence of C in 2 h at 523, 548 and 573°C forms liquid SnCl2; examination of the equilibrium reaction;; |
Conditions | Yield |
---|---|
With tetrahydrofuran In tetrahydrofuran addn. of soln. of MgCl2 in THF to suspn. of Mg powder and catalyst in THF (under Ar), hydrogenation (H2-pressure 40-60 bar, 0°C, 18 h); centrifugation; not isolated; | 96% |
With tetrahydrofuran In tetrahydrofuran addn. of soln. of MgCl2 in THF to suspn. of Mg powder and catalyst in THF (under Ar), hydrogenation (H2-pressure 50-70 bar, 0°C, 8 h); centrifugation; not isolated; | 59% |
With tetrahydrofuran In tetrahydrofuran addn. of soln. of MgCl2 in THF to suspn. of Mg powder and catalyst in THF (under Ar), hydrogenation (H2-pressure 50-70 bar, 25°C, 40 h); centrifugation; not isolated; | 41% |
With catalyst: TiCl4*2THF/ Mg-anthracene In tetrahydrofuran addn. of soln. of MgCl2 in THF to suspn. of Mg powder and catalyst in THF (under Ar), hydrogenation (H2-pressure 50-70 bar, 0°C, 40 h); centrifugation; not isolated; | 22% |
With tetrahydrofuran In tetrahydrofuran addn. of soln. of MgCl2 in THF to suspn. of Mg powder and catalyst in THF (under Ar), hydrogenation (H2-pressure 50-70 bar, 60°C, 48 h); centrifugation; not isolated; | 15% |
magnesium chloride
Mg[Al(ONC(CH3)2)4]2
Conditions | Yield |
---|---|
In tetrahydrofuran byproducts: NaCl; (moisture free); reflux (4 h), NaCl pptn.; filtration, excess solvent removal (red. pressure), crystn., recrystn. (toluene, -20°C); elem anal.; | 96% |
Conditions | Yield |
---|---|
Stage #1: levodopa With potassium tert-butylate In tetrahydrofuran; N,N-dimethyl acetamide for 0.25h; Stage #2: magnesium chloride In tetrahydrofuran; N,N-dimethyl acetamide | 96% |
trifluoroacetic acid
magnesium chloride
magnesium(II) 2,2,2-trifluoroacetate
Conditions | Yield |
---|---|
at 20 - 100℃; for 1h; | 95% |
Conditions | Yield |
---|---|
In water byproducts: NaCl; Trofimenko, S., J. Am. Chem. Soc., 89 (1967), 3170; crystd. (toluene/CH2Cl2), sublimed (vac.); elem. anal., TGA; | 94% |
Conditions | Yield |
---|---|
Stage #1: [Rh(1,10-phenanthroline)(NH3)4](CF3SO3)3; 5,6-chrysenedione; sodium hydroxide In water; acetonitrile Stage #2: magnesium chloride With sephadex QAE anionexchange column | 94% |
tetrahydrofuran
tert-butyl acetoacetate sodium salt
magnesium chloride
Conditions | Yield |
---|---|
at 20℃; for 72h; Inert atmosphere; Schlenk technique; Glovebox; | 94% |
Conditions | Yield |
---|---|
In 1,2-dimethoxyethane mixt. of MgCl2, NaBH4 in DME was stirred for 10 h under inert atm; filtered, washed with DME, solvent was vac. distilled, extd. with CH2Cl2, CH2Cl2 was distilled in vacuo; elem. anal.; | 93% |
for 7 - 22h; Inert atmosphere; Glovebox; Schlenk technique; | 85% |
2,5‐dihydroxyterephthalate
magnesium chloride
Conditions | Yield |
---|---|
Stage #1: 2,5‐dihydroxyterephthalate; magnesium chloride; iron(II) chloride In methanol; N,N-dimethyl-formamide at 120℃; for 16h; Stage #2: In N,N-dimethyl-formamide at 120℃; for 9h; Stage #3: In methanol at 60℃; | 93% |
Conditions | Yield |
---|---|
In methanol; N,N-dimethyl-formamide at 120℃; for 16h; | 93% |
Conditions | Yield |
---|---|
In benzene soln. of Ti(OPr-i)4 (6.37 mol) in benzene added to slurry of MgCl2 (3.15mol) in benzene; stirred at room temp. until dissolution of MgCl2 (24 h ); reflux for 1 h; evapd. (vac. 0.5 mm, room temp.); crystd. at -20°C (hexane/CH2Cl2= 2:1); elem. anal.; | 91% |
Conditions | Yield |
---|---|
In diethyl ether ball milled and refluxed in Et2O; | 90% |
In neat (no solvent) (Ar); mechanical action (3 h, room temp.); extn. (Et2O); | 76% |
In not given |
Conditions | Yield |
---|---|
750 °C for 1 h in inert gas, molar ratio of K2TaF4:chloride = 1:2; | 90% |
700-1000 °C in inert gas, molar ratio of K2TaF7:chloride = 1:2; |
Molecule structure of Magnesium chloride anhydrous (CAS NO.7786-30-3):
IUPAC Name: Magnesium dichloride
Molecular Weight: 95.211 g/mol
Molecular Formula: Cl2Mg
Density: 2.32 g/mL at 25 °C(lit.)
Melting Point: 714 °C(lit.)
Boiling Point: 1412 °C
Refractive Index: n20/D 1.336
Storage Temp.: 2-8 °C
Water Solubility: 400 G/L (20 °C)
Sensitive: hygroscopic
H-Bond Acceptor: 2
Exact Mass: 93.922747
MonoIsotopic Mass: 93.922747
Heavy Atom Count: 3
Complexity: 2.8
Canonical SMILES: [Mg+2].[Cl-].[Cl-]
InChI: InChI=1S/2ClH.Mg/h2*1H;/q;;+2/p-2
InChIKey: TWRXJAOTZQYOKJ-UHFFFAOYSA-L
EINECS: 232-094-6
Product Categories: Inorganics;Crystal Grade Inorganics;Inorganic Salts;Magnesium Salts;MagnesiumMetal and Ceramic Science;Salts;Synthetic Reagents;G - M;Salt Solutions;Volumetric Solutions;PCR OptimizationMolecular Biology;PCR Reaction Components;PCR/Amplification;Optimization Reagents;BioUltraProtein Structural Analysis;DNA&RNA Purification;Molecular Biology;Molecular Biology Reagents;Optimization ReagentsMolecular Biology;Reagents;X-Ray Crystallography;BiochemicalsSynthetic Reagents;Magnesium;Companion Products and ReagentsSynthetic Reagents;Insect Platform;Serum-free Media
Magnesium chloride anhydrous (CAS NO.7786-30-3) is used for the manufacture of metal magnesium, disinfectants, fire extinguishing agents, frozen brine, ceramics and also used in flipper fabric, paper making, and in the manufacture of oxychloride cement, etc.
In the Dow process, Magnesium chloride anhydrous is regenerated from magnesium hydroxide using hydrochloric acid:
Mg(OH)2(s) + 2 HCl → MgCl2(aq) + 2 H2O(l)
It can also be prepared from magnesium carbonate by a similar reaction.
1. | mmo-omi 8000 ppm | APMBAY Applied Microbiology. 6 (1958),45. | ||
2. | cyt-hmn:hla 2 mmol/L | JCLLAX Journal of Cellular Physiology. 78 (1971),217. | ||
3. | dns-rat-ipr 2500 µmol/kg | JOENAK Journal of Endocrinology. 65 (1975),45. | ||
4. | dni-rat:lvr 3300 µmol/L | BIJOAK Biochemical Journal. 146 (1975),697. | ||
5. | oms-mus:ast 4 mmol/L | AMOKAG Acta Medicia Okayama. 33 (1979),141. | ||
6. | orl-rat LD50:2800 mg/kg | JPETAB Journal of Pharmacology and Experimental Therapeutics. 35 (1929),1. | ||
7. | ipr-rat LDLo:225 mg/kg | JPETAB Journal of Pharmacology and Experimental Therapeutics. 35 (1929),1. | ||
8. | scu-rat LDLo:900 mg/kg | ENDOAO Endocrinology (Baltimore). 24 (1939),523. | ||
9. | ipr-mus LD50:1338 mg/kg | COREAF Comptes Rendus Hebdomadaires des Seances de lAcademie des Sciences. 256 (1963),1043. | ||
10. | ivn-mus LD50:14 mg/kg | TXAPA9 Toxicology and Applied Pharmacology. 22 (1972),150. | ||
11. |
|
Reported in EPA TSCA Inventory. EPA Genetic Toxicology Program.
Hazard Codes: Xi
Risk Statements: 36/37/38-43-36/37
R36/37/38:Irritating to eyes, respiratory system and skin.
R43:May cause sensitization by skin contact.
R36/37:Irritating to eyes and respiratory system.
Safety Statements: 26-36-24/25-22-36/37-39
S26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S36:Wear suitable protective clothing.
S24/25:Avoid contact with skin and eyes.
S22:Do not breathe dust.
S36/37:Wear suitable protective clothing and gloves.
S39:Wear eye / face protection.
WGK Germany: 1
RTECS: OM2800000
F: 3-10
Poison by intraperitoneal and intravenous routes. Moderately toxic by ingestion and subcutaneous routes. Human mutation data reported. In humid environments it causes steel to rust very rapidly. When heated to decomposition it emits toxic fumes of Cl−. See also MAGNESIUM.
Magnesium chloride anhydrous (CAS NO.7786-30-3) is also named as Aerotex Accelerator MX ; CCRIS 3961 ; Caswell No. 531 ; DUS-top ; EPA Pesticide Chemical Code 013902 ; HSDB 657 ; Magnesium chloride ; Magnesium chloride (Mg2Cl4) ; Magnesium chloride (MgCl2) ; Magnogene ; NSC 529832 ; TMT 2 ; UNII-59XN63C8VM . Magnesium chloride anhydrous (CAS NO.7786-30-3) is colorless, odorless and a small piece, particle, block-type monoclinic crystal. Its various hydrates MgCl2(H2O)x. These salts are typical ionic halides, being highly soluble in water.
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