High Polymers
Gamma Butyrolactone Safety Organic Solvents CAS 96-48-0 ( GBL ) for Muscle Gain / Anti-aging
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Description
Gamma?Butyrolactone?Safe?Organic?Solvents?CAS:96-48-0?(?GBL?)?for?Bodybuilding
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Basic?info:
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Gamma-Butyrolactone
Alias:?Gamma?Butyrolactone,?1,?4-?Butyrolactone,?γ?-Butyroladone,?GBL,?BLO
CAS:?96-48-0
MF:?C4H6O2
MW:?86.09
Einecs:?202-509-5
Purity?:?99.5%
Melting?Point:-44°C
Boiling?Point:206°C
Flash?Point:99.2°C
Ignition?temperature:455°C
Refractive?Index:nd20?:1.434~1.440
Density?1.12?g/mL?at?25?°?C(lit.?)
Storage?temp.?2-8°?C
Chemical?Properties:?Colorless?clear?oily?liquid?with?acetone-like?odor
Product?Categories:?Pharmaceutical?Intermediates;Heterocycles;Miscellaneous?Reagents
Lead?time?:within?24?hours?upon?receipt?of?payment
Packing:?Galvanied?iron?barrel,net?weight:200kg
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Employ:
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GBL can be used to produce a-pyrrolidone, 1-Methyl-2-pyrrolidinone , polyvinyl pyrrolidone, and α-Acetyl-γ-butyrolactone, And, GBL can be used as anaesthetic and tranquilizer, used to produce ciprofloxacin and interferon, as the intermediate of vitamin and rolicyprine; it& acute;s the intermediate of plant growth stimulator and insecticide. GBL is a good antioxidant, plasticizer, extractant, adsorbent, dispersant, fixative and curing agent; Moreover, it can also be used in battery, capacitor and development of color film.
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Product introduction:
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Gamma-Butyrolactone (γ-butyrolactone or GBL) is a hygroscopic colorless liquid with a weak characteristic odor which is soluble in water. GBL is a common solvent and reagent in chemistry as well as being used as a flavouring, as a cleaning solvent, as a superglue remover, and as a solvent in some wet aluminium electrolytic capacitors. In humans it acts as a prodrug for GHB, and it is used as a recreational intoxicant with effects similar to alcohol.
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GBL is a lactone. It is hydrolyzed under basic conditions, for example in a sodium hydroxide solution into sodium gamma-hydroxybutyrate, the sodium salt of gamma-hydroxybutyric acid. Under acidic conditions it forms an equilibrium mixture of both compounds. These compounds then may go on to form a polymer. When treated with a non-nucleophilic base, like lithium diisopropylamide, GBL can become an alpha-carbon nucleophile. The related compound caprolactone can be used to make a polyester in this manner.
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GBL is rapidly converted into GHB by paraoxonase (lactonase) enzymes, found in the blood.[7][8] Animals which lack these enzymes exhibit no effect from GBL.[7] GBL is more lipophilic (fat soluble) than GHB, and so is absorbed faster and has higher bioavailability. Because of these pharmacokinetic differences, GBL tends to be more potent and faster-acting than GHB, but has a shorter duration; whereas the related compound 1,4-butanediol (1,4-B) tends to be slightly less potent, slower to take effect but longer-acting than GHB.
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Peptides | Specification |
MGF | 2mg |
PEG?MGF | 2mg |
CJC-1295?with?DAC | 2mg |
CJC-1295?without?DAC | 2mg |
PT-141 | 10mg |
MT-1 | 10mg |
MT-2 | 10mg |
GHRP-2 | 5mg |
GHRP-2 | 10mg |
GHRP-6? | 5mg |
GHRP-6? | 10mg |
Ipamorelin | 2mg |
Hexarelin | 2mg |
Sermorelin | 2mg |
Oxytocin | 2mg |
TB500 | 2mg |
Pentadecapeptide?BPC?157 | 2mg |
Triptorelin | 2mg |
Tesamorelin | 2mg |
Gonadorelin | 2mg |
Gonadorelin | 10mg |
DSIP | 2mg |
Selank | 5mg |
Finished?steroid?oil | Strength |
Test?prop | 100mg/ml |
Test?e | 250mg/ml?300mg/ml |
Test?cyp | 250mg/ml?300mg/ml |
Test?Suspension | 100mg/ml |
Sustanon | 200mg/ml?250mg/ml?300mg/ml |
Deca | 200mg/ml?250mg/ml |
NPP | 100mg/ml?150mg/ml |
Equipoise | 200mg/ml?250mg/ml?300mg/ml |
Tren?ace | 100mg/ml |
Tren?en | 100mg/ml?200mg/ml |
Masteron | 100mg/ml?150mg/ml |
Primobolone | 100mg/ml |
Supertest?450 | 450mg/ml |
Anomass??400 | 400mg/ml |
Rippex?225 | 225mg/ml |
Tri?Tren?180 | 180mg/ml |
Tri?Test?300 | 300mg/ml |
Tri?Deca?300 | 300mg/ml |
Test?Blend?450 | 450mg/ml |
Test?Blend?500 | 500mg/ml |
Nandro?Test?225 | 225mg/ml |
Mass?500 | 500mg/ml |
Cut?Depot?400 | 400mg/ml |
Tren?Test?225 | 225mg/ml |
Nandro?Test?Depot?450 | 450mg/ml |
Equi?Test?450 | 450mg/ml |
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