cyanomethane-sulfonic acid
Tau
Conditions | Yield |
---|---|
With hydrogen at 55℃; under 22502.3 Torr; Temperature; Pressure; Reagent/catalyst; Inert atmosphere; | 99.98% |
Conditions | Yield |
---|---|
With 2,2,6,6-tetramethyl-piperidine In water at 140℃; under 3000.3 Torr; for 0.166667h; Reagent/catalyst; Temperature; Pressure; | 98.4% |
With dihydrogen peroxide; acetic acid |
Conditions | Yield |
---|---|
With ethanolamine pH=12.5; | 95.7% |
With sulfuric acid at 80 - 100℃; pH=7.9; Temperature; pH-value; | 75% |
With sulfur dioxide In water pH=5 - 6; Reagent/catalyst; | 110 g |
ammonium 2-nitroethane-1-sulfonate
Tau
Conditions | Yield |
---|---|
With palladium 10% on activated carbon; hydrogen at 20℃; pH=4.2; Concentration; pH-value; Temperature; Reagent/catalyst; Large scale; | 95.1% |
Conditions | Yield |
---|---|
With C22H24OP(1+)*CH3O3S(1-); ammonia; copper(l) chloride at 160℃; under 73507.4 Torr; for 0.5h; Reagent/catalyst; Temperature; Pressure; | 95% |
Stage #1: sodium 2-hydroxyethanesulfonate pH=12.5; Stage #2: With ammonia In water at 250℃; under 135014 Torr; for 2h; Autoclave; | 91% |
With ammonium hydroxide; sodium hydroxide at 250℃; for 2h; Reagent/catalyst; Temperature; Autoclave; | 78.4% |
Tau
Conditions | Yield |
---|---|
With sulfur dioxide at 20℃; pH=4.2; Concentration; Temperature; pH-value; Large scale; | 95% |
thiazolidine-2-thione
Tau
Conditions | Yield |
---|---|
With formic acid; dihydrogen peroxide In water at 0 - 5℃; | 93% |
Conditions | Yield |
---|---|
Stage #1: sulfuric acid mono-(2-amino-ethyl ester) With ammonium sulfite monohydrate at 120℃; for 18h; Autoclave; Stage #2: With ammonium sulfite monohydrate; sodium hydroxide In water pH=7.2; Temperature; | 88.1% |
With water; sodium sulfite |
Conditions | Yield |
---|---|
With ammonium sulfate; sulfuric acid; ammonium sulfite monohydrate In water at 110℃; for 24h; pH=6.2 - 7.2; Autoclave; | 85% |
Conditions | Yield |
---|---|
Stage #1: 2-nitro-1-ethanol With sulfur dioxide; sodium hydroxide for 15h; pH=5.9; Autoclave; Stage #2: sodium 2-nitroethanesulfonate With hydrogen Autoclave; | 81% |
Tau
Conditions | Yield |
---|---|
With ammonia pH=6.5; Autoclave; | 75.7% |
Tau
Conditions | Yield |
---|---|
Stage #1: monoethanolammonium hydrogensulfate With 1-butyl-3-methylimidazolium chloride at 120℃; Stage #2: With sodium sulfite at 110℃; for 8h; Temperature; Reagent/catalyst; | 72% |
Conditions | Yield |
---|---|
Stage #1: ethene With sulfur trioxide In acetonitrile under 38000 Torr; for 288h; Stage #2: With hydrogenchloride In water Heating; | 40% |
3-sulfopropanoic acid
Tau
Conditions | Yield |
---|---|
With sodium azide; chloroform; sulfuric acid at 45℃; | |
With sodium azide; sulfuric acid for 2.5h; Heating; from 3-14C labeled educt; |
cysteic acid
Tau
Conditions | Yield |
---|---|
With water at 235 - 240℃; | |
Decarboxylation; |
Conditions | Yield |
---|---|
Decarboxylierung unter anaerober Einwirkung von Leber-Extrakt; |
Conditions | Yield |
---|---|
With ammonium iron (II) sulfate; dihydrogen peroxide at 100℃; | |
With ammonium iron (II) sulfate; dihydrogen peroxide at 100℃; |
2-bromoethanesulfonyl chloride
Tau
Conditions | Yield |
---|---|
Hydrolysis.anschl. mit wss. NH3; |
2-nitro-ethanesulfonic acid
Tau
Conditions | Yield |
---|---|
With water; nickel Hydrogenation; | |
With water; nickel Hydrogenation; |
Conditions | Yield |
---|---|
at 0 - 25℃; Equilibrium constant; |
1,2-Thiazetidine 1,1-dioxide
Tau
Conditions | Yield |
---|---|
In water | |
With sodium hydroxide; potassium chloride at 30℃; Kinetics; |
1-methyl-4-(phenylacetyl)pyridinium cation
2-aminoethanesulfonate
A
Tau
B
C14H13NO
Conditions | Yield |
---|---|
In water at 25℃; Rate constant; Equilibrium constant; |
Conditions | Yield |
---|---|
In 1,4-dioxane; water at 25℃; Equilibrium constant; |
Tau
Conditions | Yield |
---|---|
With sodium hydroxide; sodium azide; sulfuric acid 1.) heating, 2 h .) heating, 2.5 h; Multistep reaction; |
Conditions | Yield |
---|---|
With sodium bromate; sodium perchlorate In water at 25℃; Product distribution; Mechanism; various reaction conditions; | |
With potassium iodate In water at 25℃; Mechanism; |
Conditions | Yield |
---|---|
With phosphate buffer Rate constant; also hydrolysis in physiological solution and aq. EtOH; |
Conditions | Yield |
---|---|
With chlorine dioxide; sodium perchlorate In water at 25℃; Rate constant; Mechanism; |
Conditions | Yield |
---|---|
With sodium perchlorate; hypochloric acid In water at 25℃; Rate constant; Mechanism; |
Conditions | Yield |
---|---|
With sodium hydroxide a) 0 deg C, 30 min, b) 20 deg C, 2 h; | 100% |
With sodium hydroxide In water for 0.5h; | 100% |
With sodium hydroxide In 1,4-dioxane; water at 20℃; for 1h; | 82% |
Conditions | Yield |
---|---|
With sodium hydroxide In water at 60℃; Sonication; | 100% |
With sodium hydrogencarbonate In water at 20℃; for 2h; | 100% |
With sodium hydrogencarbonate In water | |
With sodium hydroxide In water |
Conditions | Yield |
---|---|
In water; acetone at 20℃; | 100% |
In water; acetone at 20℃; | 100% |
99% | |
In water; acetone at 20℃; for 12h; | 95% |
In water; acetone at 25℃; for 16h; |
Tau
4,6,4',6'-tetrachloro-2,2'-(3,6-dioxa-octane-1,8-diyldioxy)-bis-[1,3,5]triazine
Conditions | Yield |
---|---|
With sodium carbonate In tetrahydrofuran; water at 0 - 20℃; | 100% |
Tau
Conditions | Yield |
---|---|
With calcium hydroxide In water at 20℃; for 2h; Time; Reflux; | 100% |
Conditions | Yield |
---|---|
With sodium hydroxide; nitrogen In water | 99.8% |
Conditions | Yield |
---|---|
With potassium hydroxide In water | 99.1% |
Conditions | Yield |
---|---|
With sodium hydroxide In water at 20℃; for 2h; | 98.6% |
Conditions | Yield |
---|---|
In methanol at 70℃; for 4h; Temperature; Solvent; Mannich Aminomethylation; Green chemistry; | 98.5% |
Conditions | Yield |
---|---|
With water; sodium hydroxide In 1,4-dioxane at 0 - 20℃; | 98% |
Conditions | Yield |
---|---|
With sodium hydroxide at -10 - 0℃; for 8h; | 97.6% |
Tau
1,10-phenanthroline-2,9-dicarboxaldehyde
Conditions | Yield |
---|---|
With NaHCO3 In water (Ar or N2); a flask charged with 1,10-phenanthroline-2,9-dicarboxaldehyde, sulfanilic acid, Cu2O, NaHCO3, sealed, purified of O2, H2O added, sealed, stirred at room temp.; evapd. (vac.); | 97% |
Conditions | Yield |
---|---|
With sodium hydroxide at 0 - 10℃; for 2h; | 96.9% |
Tau
di-tert-butyl dicarbonate
Conditions | Yield |
---|---|
With sodium hydrogencarbonate In tetrahydrofuran; methanol at 10℃; for 24h; Temperature; Cooling with ice; | 96% |
With sodium hydroxide; water In tetrahydrofuran for 15h; Ambient temperature; Yield given; | |
With sodium hydroxide In tetrahydrofuran; water at 20℃; | |
With dmap; triethylamine In dichloromethane at 0℃; |
Conditions | Yield |
---|---|
With sodium hydrogencarbonate; tert-butyl alcohol In water-d2 (Ar or N2); pyridine-2-carboxaldehyde, taurine, Cu2O, NaHCO3 added to flask; sealed; mag. stirring-bar added; water added; flask sealed; stirredfor 8 h at 22°C; volatiles removed under dynamic vac.; methanol and tert-butanol added; pptd.; crystals allowed to settle; supernatant removed with cannula filter; dried under dynamic vac. for 4 h; elem. anal.; | 96% |
Tau
lithium 2-aminoethanesulfonate
Conditions | Yield |
---|---|
Stage #1: Tau With lithium hydroxide monohydrate In water at 20℃; Stage #2: In toluene at 100℃; for 12h; | 96% |
Conditions | Yield |
---|---|
With potassium hydroxide In water at -10 - 0℃; for 6h; | 96% |
Conditions | Yield |
---|---|
With sodium hydroxide In ethanol for 3h; Heating; | 95.8% |
Conditions | Yield |
---|---|
Stage #1: Tau; cholic acid With N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline; triethylamine In N,N-dimethyl-formamide at 90℃; for 2h; Stage #2: With sodium hydroxide In methanol at 20℃; for 1h; | 95% |
With N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline; sodium hydroxide In water; dimethyl sulfoxide; acetonitrile; tert-butyl alcohol at 20 - 80℃; | 88% |
Conditions | Yield |
---|---|
With N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline; sodium hydroxide In water; dimethyl sulfoxide; acetonitrile; tert-butyl alcohol at 20 - 80℃; | 95% |
Conditions | Yield |
---|---|
With N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline; sodium hydroxide In water; acetonitrile; tert-butyl alcohol at 20 - 80℃; | 95% |
Conditions | Yield |
---|---|
Stage #1: Tau With sodium hydroxide In ethanol for 1h; Reflux; Stage #2: (±)-gossypol acetic acid In ethanol for 5h; Reflux; | 94% |
Stage #1: Tau With sodium hydroxide In ethanol for 1h; Reflux; Stage #2: (±)-gossypol acetic acid In ethanol for 5h; Reflux; | 94% |
Conditions | Yield |
---|---|
With N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline; sodium hydroxide In water; acetonitrile; tert-butyl alcohol at 20 - 80℃; | 93% |
Structure Descriptors of Taurine (CAS NO.107-35-7):
IUPAC Name: 2-aminoethanesulfonic acid
Molecular Formula: C2H7NO3S
Molecular Weight: 125.14g/mol
Mol File: 107-35-7.mol
EINECS: 203-483-8
Appearance: Large white crystals or white powder
Melting Point: >300 °C(lit.)
Storage Temperature: 2-8°C
Density: 1.494 g/cm3
Water Solubility: 5-10 g/100 mL at 23.5 ºC
Stability: Stable. Incompatible with strong oxidizing agents.
Surface Tension: 68.1 dyne/cm
Index of Refraction: 1.515
Molar Refractivity: 25.27 cm3
Molar Volume: 83.7 cm3
XLogP3-AA: -4.1
H-Bond Donor: 2
H-Bond Acceptor: 4
Canonical SMILES: C(CS(=O)(=O)O)N
InChI: InChI=1S/C2H7NO3S/c3-1-2-7(4,5)6/h1-3H2,(H,4,5,6)
InChIKey: XOAAWQZATWQOTB-UHFFFAOYSA-N
Product Categories: Food and Feed Additive; Food & Feed ADDITIVES; Sulphur Derivatives; pharmacetical; Natural Plant Extract; Nutritional fortification substances; Amino Acids; GABA/Glycine receptor
The uses of Taurine are as follows:
1. Taurine is an essential dietary requirement for feline health, since cats cannot synthesize the compound. The absence of taurine causes a cat's retina to slowly degenerate, causing eye problems and (eventually) irreversible blindness — a condition known as central retinal degeneration (CRD),as well as hair loss and tooth decay. It was discovered in 1987 that taurine deficiency can also cause feline dilated cardiomyopathy. Unlike CRD, the condition is reversible with supplementation. Taurine is now a requirement of the Association of American Feed Control Officials (AAFCO) and any dry or wet food product labeled approved by the AAFCO should have a minimum of 0.1% taurine in dry food and 0.2% in wet food.
2.Recent research has provided evidence that Taurine is essential in early bird development of passerines. Many passerines, regardless of spider availability, seek out many Taurine-rich spiders to feed their young particularly in their youngest stages of life. Researchers later compared the behaviors and development of birds fed a Taurine-supplemented diet to a control diet and found that juveniles that were fed Taurine-rich diets as neonates were much larger risk takers and more adept at spatial learning tasks.
3. Taurine is used as a functional food in many energy drinks and energy products. Despite being present in many energy foods, it has not been proven to be energy-giving. A study of mice hereditarily unable to transport Taurine suggests that it is needed for proper maintenance and functioning of skeletal muscles. Additionally, it has been shown to be effective in removing fatty liver deposits in humans, preventing liver disease, and reducing cirrhosis in rats.
4. Taurine is necessary for normal skeletal muscle functioning.
5.It is believed that prematurely born infants lack the enzymes needed to convert cystathionine to cysteine and may therefore become deficient in taurine. Thus, Taurine is thought to be a dietary essential nutrient in these individuals and has been added to many infant formulas as a measure of prudence, since the early 1980s.
For mammalian taurine synthesis occurs in the pancreas via the cysteine sulfinic acid pathway. In this pathway, the sulfhydryl group of cysteine is first oxidized to cysteine sulfinic acid by the enzyme cysteine dioxygenase. Cysteine sulfinic acid, in turn, is decarboxylated by sulfinoalanine decarboxylase to form hypotaurine. It is unclear whether hypotaurine is then spontaneously or enzymatically oxidized to yield taurine.
Taurine in the pharmaceutical and lab setting is synthesized through a combination of cysteine, methionine, and vitamin E.
In 1993, approximately 5,000–6,000 t. of taurine were produced; 50% for pet food manufacture, 50% in pharmaceutical applications.Synthetic taurine is obtained from isethionic acid (2-hydroxyethanesulfonic acid), which in turn is obtained from the reaction of ethylene oxide with aqueous sodium bisulfite.Another approach is the reaction of aziridine with sulfurous acid. This leads directly to taurine.
Organism | Test Type | Route | Reported Dose (Normalized Dose) | Effect | Source |
---|---|---|---|---|---|
dog | LD50 | intravenous | > 2gm/kg (2000mg/kg) | Yakuri to Chiryo. Pharmacology and Therapeutics. Vol. 19, Pg. 2677, 1991. | |
mammal (species unspecified) | LD | oral | > 10gm/kg (10000mg/kg) | Gigiena Truda i Professional'nye Zabolevaniya. Labor Hygiene and Occupational Diseases. Vol. 33(10), Pg. 57, 1989. | |
mouse | LD50 | intramuscular | > 7gm/kg (7000mg/kg) | Drugs in Japan Vol. -, Pg. 51, 1990. | |
mouse | LD50 | intraperitoneal | 6630mg/kg (6630mg/kg) | Yaoxue Tongbao. Bulletin of Pharmacology. Vol. 18, Pg. 658, 1983. | |
mouse | LD50 | intravenous | > 7gm/kg (7000mg/kg) | Drugs in Japan Vol. -, Pg. 51, 1990. | |
mouse | LD50 | oral | > 7gm/kg (7000mg/kg) | Drugs in Japan Vol. -, Pg. 51, 1990. | |
mouse | LD50 | subcutaneous | 6gm/kg (6000mg/kg) | Quarterly Journal of Pharmacy & Pharmacology. Vol. 19, Pg. 48, 1946. | |
rabbit | LD50 | intravenous | > 1gm/kg (1000mg/kg) | Drugs in Japan Vol. -, Pg. 51, 1990. | |
rat | LD50 | intravenous | > 7gm/kg (7000mg/kg) | BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY) LUNGS, THORAX, OR RESPIRATION: RESPIRATORY DEPRESSION SKIN AND APPENDAGES (SKIN): HAIR: OTHER | Yakuri to Chiryo. Pharmacology and Therapeutics. Vol. 19, Pg. 2671, 1991. |
rat | LD50 | oral | > 5gm/kg (5000mg/kg) | Yakuri to Chiryo. Pharmacology and Therapeutics. Vol. 19, Pg. 2671, 1991. |
Safety Information of Taurine (CAS NO.107-35-7):
Hazard Codes: Xi
Risk Statements: 36/37/38
R36/37/38:Irritating to eyes, respiratory system and skin.
Safety Statements: 26-36-24/25
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.
WGK Germany: 2
RTECS: WX0175000
HS Code: 29211980
Taurine , its CAS NO. is 107-35-7, the synonyms are 2-Aminoethanesulfonic acid ; 2-Aminoethylsulfonic acid ; 2-Sulfoethylamine ; Tauphon ; Taurinum ; beta-Aminoethylsulfonic acid ; Ethanesulfonic acid, 2-amino- ; L-Taurine .
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