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taurine
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Basic
Common Name Taurine
CAS Number 107-35-7
Molecular Weight 125.147
Density 1.5±0.1 g/cm3
Boiling Point N/A
Molecular Formula C2H7NO3S
Melting Point >300 °C(lit.)
MSDS Chinese USA
Flash Point N/A
Symbol GHS07
Signal Word Warning
Physical Chemistry
Density 1.5±0.1 g/cm3
Melting Point >300 °C(lit.)
Molecular Formula C2H7NO3S
Molecular Weight 125.147
Exact Mass 125.014664
PSA 88.77000
LogP -2.46
Index of Refraction 1.515
Storage condition 2-8°C
Stability Stable. Incompatible with strong oxidizing agents.
Water Solubility 5-10 g/100 mL at 23.5 ºC
Toxicity
CHEMICAL IDENTIFICATION
RTECS NUMBER :
WX0175000
CHEMICAL NAME :
Taurine
CAS REGISTRY NUMBER :
107-35-7
LAST UPDATED :
199710
DATA ITEMS CITED :
16
MOLECULAR FORMULA :
C2-H7-N-O3-S
MOLECULAR WEIGHT :
125.16
WISWESSER LINE NOTATION :
Z2SWQ
HEALTH HAZARD DATA
ACUTE TOXICITY DATA
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
>5 gm/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intravenous
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
>7 gm/kg
TOXIC EFFECTS :
Behavioral - somnolence (general depressed activity) Lungs, Thorax, or Respiration - respiratory depression Skin and Appendages - hair
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
>7 gm/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intraperitoneal
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
6630 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Subcutaneous
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
6 gm/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intravenous
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
>7 gm/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intramuscular
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
>7 gm/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intravenous
SPECIES OBSERVED :
Mammal - dog
DOSE/DURATION :
>2 gm/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intravenous
SPECIES OBSERVED :
Rodent - rabbit
DOSE/DURATION :
>1 gm/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
TYPE OF TEST :
LD - Lethal dose
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Mammal - species unspecified
DOSE/DURATION :
>10 gm/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
TYPE OF TEST :
TDLo - Lowest published toxic dose
ROUTE OF EXPOSURE :
Intravenous
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
182 gm/kg/13W-C
TOXIC EFFECTS :
Lungs, Thorax, or Respiration - other changes Nutritional and Gross Metabolic - changes in sodium Nutritional and Gross Metabolic - changes in chlorine
TYPE OF TEST :
TDLo - Lowest published toxic dose
ROUTE OF EXPOSURE :
Oral
DOSE :
878 gm/kg
SEX/DURATION :
multigenerations
TOXIC EFFECTS :
Reproductive - Effects on Newborn - growth statistics (e.g.%, reduced weight gain)
MUTATION DATA
TEST SYSTEM :
Rodent - rat
DOSE/DURATION :
7560 mg/kg/6W
REFERENCE :
CRNGDP Carcinogenesis (London). (Oxford Univ. Press, Pinkhill House, Southfield Road, Eynsham, Oxford OX8 1JJ, UK) V.1- 1980- Volume(issue)/page/year: 9,387,1988 *** NIOSH STANDARDS DEVELOPMENT AND SURVEILLANCE DATA *** NIOSH OCCUPATIONAL EXPOSURE SURVEY DATA : NOES - National Occupational Exposure Survey (1983) NOES Hazard Code - X7233 No. of Facilities: 167 (estimated) No. of Industries: 5 No. of Occupations: 13 No. of Employees: 19927 (estimated) No. of Female Employees: 3025 (estimated)
Safety
Symbol GHS07
Signal Word Warning
Hazard Statements H315-H319-H335
Precautionary Statements P305 + P351 + P338
Personal Protective Equipment dust mask type N95 (US);Eyeshields;Gloves
Hazard Codes Xi: Irritant;
Risk Phrases R36/37/38
Safety Phrases S26-S36-S24/25
RIDADR NONH for all modes of transport
WGK Germany 2
RTECS WX0175000
HS Code 2921199090
Preparation

N/A

FAQ

1.What is Taurine?

Taurine is a non-proteinogenic (i.e., it is not incorporated into proteins during translation) sulfur-containing beta-amino acid that is omnipresent in the body and is particularly abundant in electrically excitable tissues such as the heart, retina, brain, and skeletal muscle. A small amount of taurine is produced in the liver from the metabolism of cysteine (which is itself derived from the essential amino acid methionine). Taurine can also be obtained directly from certain foods like beef, dark-meat poultry, and, most abundantly, shellfish such as scallops and mussels. Taurine is considered a conditionally essential nutrient, meaning that we can produce it in our bodies, but under certain conditions may not produce enough to meet all of our functional needs. Because taurine can be produced in the body, the average adult probably doesn’t need to be concerned about overt symptoms of taurine deficiency. (In this, humans are unlike cats and monkeys, who develop retinopathy and cardiomyopathy with inadequate taurine intake) However, low plasma taurine levels are associated with various conditions, such as cardiovascular disease and type 2 diabetes. In accordance with its ubiquitous presence in the body, taurine has diverse physiological functions. It is known as a cell-protecting agent and is involved in osmoregulation, modulation of mitochondrial function and endoplasmic reticulum stress, cell membrane stabilization, conjugation of bile acids, calcium homeostasis, energy metabolism, neuromodulation, and anti-inflammatory and antioxidant actions.

2.What are taurine’s main benefits?

Interest in taurine primarily stems from its potential beneficial effects on athletic performance and potential mitigation of cardiovascular risk factors. Taurine was first used to treat heart failure patients and demonstrated the ability to improve symptoms — as evidenced by improved cardiac output and stroke volume — which spurred research to determine whether it elicited other cardioprotective effects. While some evidence supports the use of taurine in the treatment of heart failure, there are few studies on the topic and further high-quality randomized controlled trials are needed to confirm potential benefits. More recent evidence demonstrates that taurine modestly reduces blood pressure, and it seems to be more effective in people with prehypertension or hypertension. Taurine may also reduce total cholesterol and triglyceride levels. Taurine is a common component of energy drinks, which have been shown to enhance various aspects of physical performance (e.g., endurance exercise performance, vertical jump height).[26] However, energy drinks also contain caffeine, among other ingredients, so it is unclear how much of their benefit can be attributed to taurine. Because taurine levels are much higher in type I (“slow twitch”) than type II (“fast twitch”) muscle fibers, most studies have investigated whether taurine supplementation improves endurance exercise performance. Taurine appears to have a small positive effect on time to exhaustion in both untrained healthy people and older adults with heart failure. In contrast, taurine does not seem to benefit time trial performance. Research on whether taurine improves muscle strength and power is limited and inconclusive, and the effect of taurine on reducing symptoms of delayed onset muscle soreness and accelerating recovery following exercise is equivocal and requires further research.

3.How does taurine work?

Most of taurine’s benefits are thought to derive from its role as a cell-protective agent: it regulates cell volume, calcium homeostasis, and stabilizes cell membranes, and also exerts antioxidant effects. The primary mechanism by which taurine acts as an antioxidant is unclear. Taurine may have the ability to directly scavenge free radicals, but it’s more likely that taurine works by regulating antioxidant enzymes and inhibiting the generation of mitochondrial reactive oxygen species. Taurine may provide cardioprotective effects by decreasing oxidative stress and a few other mechanisms. It can modify blood lipids by binding to bile acids and facilitating the breakdown and excretion of cholesterol. Additionally, it reduces blood pressure by enhancing vasodilation (i.e., by relaxing of blood vessels), leading to an increase in blood flow. Taurine may also reduce blood pressure by reducing the production of angiotensin II, a potent vasoconstrictor. Muscle contraction is triggered by the release of calcium from the sarcoplasmic reticulum. Taurine may improve physical performance by increasing the calcium-storing ability of the sarcoplasmic reticulum, as well as increasing the sensitivity of force-generating proteins (i.e., actin and myosin) to calcium, thus increasing muscle force. With special reference to endurance exercise, taurine may aid performance by increasing the use of fat for fuel and reducing the contribution from glycogen, as well as improving mitochondrial function.

4.How It’s Made?

Adult bodies make their own taurine from a nonessential amino acid called cysteine. High-protein foods have enough cysteine for the human body, so most people don’t need supplements. Babies, on the other hand, can’t make their own taurine. They get it from breast milk or formula that has taurine supplements.

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