2016年11月30日星期三

5F-PB-22

CAS:1445579-79-2
Formula:C22H20FN3O2
Molecular weight:377.400
Compound purity:> 99.7%
Appearance:Powder
IUPAC:quinolin-8-yl-1-(5-fluoropentyl)-1H-indazole-3-carboxylate
Synonyms:5-fluoro NPB-22, 5F-PB-22 indazole analogue, QCBL(N)-2201
Technical Information
Formal Name1-(5-fluoropentyl)-8-quinolinyl ester-1H-indazole-3-carboxylic acid
CAS Number1445579-79-2
Molecular FormulaC22H20FN3O2
Formula Weight377.4
Purity≥98%
FormulationA crystalline solid
λmax226, 302 nm
SMILESO=C(OC1=C(N=CC=C2)C2=CC=C1)C3=NN(CCCCCF)C4=C3C=CC=C4
InChI Code1S/C22H20FN3O2/c23-13-4-1-5-15-26-18-11-3-2-10-17(18)21(25-26)22(27)28-19-12-6-8-16-9-7-14-24-20(16)19/h2-3,6-12,14H,1,4-5,13,15H2
InChI KeyDZNDVBLSHUYZLI-UHFFFAOYSA-N
WARNING - This product is not for human or veterinary use.
Shipping & Storage
Storage-20°C
ShippingRoom temperature in continental US; may vary elsewhere
StabilityAs supplied, 2 years from the QC date provided on the Certificate of Analysis, when stored properly

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Notice: This product is only suitable for laboratory use, or the use of animals. It can not be used directly on the human body

Kigtropin HGH



Introduce:
Recombinant Human Growth Hormone for Injection
【NAME OF THE MEDICINAL PRODUCT】
Generic Name: Recombinant Human Growth Hormone
Trade Name: KIGTROPIN
【INGREDIENTS】
Recombinant Human Growth Hormone and excipients.
Molecular Formula:C990H1528N262O300S7 with 191 amino acids residues.
Molecular Weight:22125D
Origin of the Active Ingredient: KIGTROPIN is a Recombinants Human Growth Hormone.
KIGTROPIN is produced by recombinant DNA technology in E.coli secretion expression system.
KIGTROPIN has the same amino acid sequence with 191 residues as the native human growth hormone produced in the human body.
【CHARACTERS】
White Lyophilized powder.
【INDICATION】
Growth failure of children due to endogenous growth hormone deficiency (GHD).
In adults with growth hormone deficiency,KIGTROPIN reduces fat mass,increases muscle mass and improves energy,vitality and subjective well-being. In patients suffering from severe burns,AIDS associated muscle wasting,or undergoing major operations,KIGTROPIN promotes wound healing,attenuates the protein-catabolic response and improves whole-body nitrogen condition after operation.
【SPECIFICATIONS】
10IU/3.7mg/1.0ml/vial
【DOSAGE AND ADMINISTRATION】
Before administration, add 1ml of sterile water for injection to the rhGH vial of Lyophilized powder along the wall slowly. Shake it gently to fully dissolve the powder to get clarified solution. DO NOT shake violently.
For anti-aging, general health & healing, fat mobilization, a dose of 2-3 IU's per day will be sufficient for the majority. A dose of 1.5 to 2.0 IU's is considered to be a full replacement dose for those in their middle-age and beyond.
For gaining lean muscle and substantially improving body composition, a dose of 4-8 IUs per day will be necessary. Most people will respond very well at a dose of 4-5 IU's per day. For maximum benefit in this regard, the addition of Testosterone, Insulin, and low-dose t3 would be something to seriously consider. More on this in our comparative cycle guide of HGH/Insulin/IGF.
The recommended dosage for injection is 0.1-0.15IU/kg/day, inject before sleeping daily at the same time and the injectionsite should be changes frequently to prevent lipoatrophy at the site, or follow the physician’s advice.
【ADVERSE REACTIONS】
Growth hormone may induce transient hyperglycosemia, which usually recover to normal level over time or after drug discontinuation.
About 1% children with microsomia in the clinical trial presented side effects, which usually presented transient reactions at the injection site (pain, tingling numbness, red swelling, etc) and the symptoms of fluid retention (peripheral edema, arthralgia or myalgia).These side effects usually appear at early stage and the incidence rate decreases over time which rarely affects daily activities.
Long-term injection of recombinant human growth hormone results in antibody production in minority people, however, the affinity of the antibody is low without exact clinical significance. The antibody may be induced if the anticipant effect of growth is not achieved, which may affect the efficacy if the affinity is over 2 mg/L.
【CONTRAINDICATIONS】
Children with closure of epiphysis are forbidden.
Patients with the progressive symptoms of tumor are forbidden.
Critical ill patients in acute shock stage of serious systematic infection are forbidden.
【WARNINGS AND PRECAUTIONS】
rhGH therapy should be conducted on exactly diagnosed GHD patients under advice of experienced doctor.
For diabetes patients, dosage of anti-glucourea drugs should be adjusted during rhGH therapy.
For patients whose GHD were caused by encephaloma or encephalic wound, the progress and relapse possibility of potential diseases should be closely monitored.
For ACTH deficiency patients, dosage of ATCH should be adjusted because the growth improvement effect of rhGH could be inhibited by simultaneous using of ACTH.
Thyroid gland function should be tested regularly because clinical hypothyroidism may occur to some patients during rhGH therapy. For those hypothyroid, thyroid supplementation is necessary for ensuring the therapeutic effects of rhGH.
Careful consideration should be taken if claudicating occurred during rhGH therapy because the patients who suffered from endocrine system disease (including GHD) have such a tendency that their epiphysis plates of femur are relatively easy to separate.
Growth hormone may lead to over insulin state. Attention should be paid to if lower glucose intolerance appeared.
Do not take over-dose of rhGH, one time over-dose rhGH administration can lead to high blood sugar. Long-term over-does rhGH administration can lead to acromegaly.
Injection site should often variation in case lipoatrophy.
Athletes should administer the drug with caution.
【USAGE IN PREGNANCY AND LACTATION】
It is not suitable to use.
【DRUG INTERACTIONS】
Concurrent administration of glucocorticoid may inhibit the response of the hormone, therefore, the dosage of glucocorticoid is usually not over the equivalent dosage of 10~15 mg hydrocortisone/square meter body surface area.
Concurrent administration of non-androgen steroid may further promote the growth rate.
【PHARMACOLOGY AND TOXICOLOGY】
rhGH exerts the same actions of endogenous human growth hormone. It can stimulate proliferation and differentiation of epiphysis chondrocyte, stimulate growth of cartilage matrix cells, stimulate proliferation and differentiation of osteoblast; thus accelerate the liner growth rate and improve epiphysis width.
rhGH can promote protein synthesis in whole body; reverse the negative nitrogen equilibrium caused by wound and surgery;correct the hypoproteinemia due to severe infection or hepatocirrhosis; stimulate synthesis of immune globin and proliferation of lymph adenoid, macrophage and lymphocyte, thus enhance the ability of infection resistance; stimulate proliferation of collagenocyte, fibroblast and macrophage in sites of burn and surgery, thus accelerate wound healing; promote synthesis of cardiocytes, thus improve cardiac contractility and reduce cardiac oxygen consumption; regulate lipometabolism, thus depress serum cholesterol and low density lipoprotein's level; complement insufficiency or deficiency of growth hormone, regulate adult's lipometabolism, osteometabolism, heart and kidney function.
【PHARMACOKINETICS】
It is reported that the equal pharmacological effect could be achieved via subcutaneous (sc) or intramuscular (IM) administration. Even though sc may lead a higher concentration of GH in plasma, IM could also yield the same IGF-l level. The absorption of GH is the relatively slow, max often occurs at 3-5 hours after injection. Clearance of GH is via liver and kidney, the half-life of clearance is about 2-3 hours. Uncatabolized GH excreted in urea is almost immeasurable. All of the GH in circulation system exists as a complex form with GH binding proteins that make the half-life of GH prolonged.
【STORAGE】
Keep at 2~8oC in the refrigerator,away from light.
Before reconstitution:
--If refrigerated between 2-8oC, it's good until expiration date.
--At room temperature (under 37oC) it's good for over 30 days.
After reconstitution:
--Use Bacteriostatic Water to reconstitute and keep in 2~8oC, it will be good for 20 days.
--Use Sterile Water to reconstitute and keep in 2~8oC. it will be good for 72 hours.
【PACKAGE】
Tube-shaped antibiotics glass bottle, 10 bottles/inner box.
【SHELF LIFE】
Two years.
【EXECUTIVE STANDARD】
Pharmacopoeia of People’s Republic of China 2005 Edition 2
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Fu-F





Furanylfentanyl (Fu-F) is an opioid analgesic which has an ED50 value of 0.02mg/kg in mice.

Appearance: White powder

Purity: >99%

Package: 1kg/Aluminum foil bag or as customer's request.

Application: For chemical research

Production Capacity: 500 Kilogram/Month

Storage: Kept in a cool,dry and ventilated place

Side effects of fentanyl analogs are similar to those of fentanyl itself, which include itching, nausea and potentially serious respiratory depression, which can be life-threatening. Fentanyl analogs have killed hundreds of people throughout Europe and the former Soviet republics since the most recent resurgence in use began in Estonia in the early 2000s, and novel derivatives continue to appear.

Life-threatening adverse reactions due to furanylfentanyl use have been observed in Sweden. At least seven deaths in Cook County, Illinois, have been linked to furanylfentanyl.

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Furanylfentanyl





Furanylfentanyl (Fu-F) is an opioid analgesic which has an ED50 value of 0.02mg/kg in mice.

Appearance: White powder

Purity: >99%

Package: 1kg/Aluminum foil bag or as customer's request.

Application: For chemical research

Production Capacity: 500 Kilogram/Month

Storage: Kept in a cool,dry and ventilated place

Side effects of fentanyl analogs are similar to those of fentanyl itself, which include itching, nausea and potentially serious respiratory depression, which can be life-threatening. Fentanyl analogs have killed hundreds of people throughout Europe and the former Soviet republics since the most recent resurgence in use began in Estonia in the early 2000s, and novel derivatives continue to appear.

Life-threatening adverse reactions due to furanylfentanyl use have been observed in Sweden. At least seven deaths in Cook County, Illinois, have been linked to furanylfentanyl.

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Notice: This product is only suitable for laboratory use, or the use of animals. It can not be used directly on the human body

5-fluoro THJ 018




THJ-2201 is an indazole-based synthetic cannabinoid that presumably acts as a potent
agonist of the CB1 receptor and has been sold online as a designer drug.
It is a structural analog of AM-2201 in which the central indole ring has been replaced by
indazole.
Cannabinoids are commonly smoked or vaporized to achieve a quick onset of effects and
rapid offset. THJ-2201 is orally active when dissolved in a lipid, which can increase the
duration significantly. Like other cannabinoids, it is insoluble in water but dissolves in
ethanol and lipids.
TECHNICAL INFORMATION
Formal Name[1-(5-fluoropentyl)-1H-indazol-3-yl]-1-naphthalenyl-methanone
CAS Number1801552-01-1
Synonyms
· AM2201 indazole analog
· 5-fluoropentyl JWH 018 indazole analog
· 5-fluoro THJ 018
Molecular FormulaC23H21FN2O
Formula Weight360.4
Purity≥98%
FormulationA crystalline solid
λmax219, 320 nm
SMILESO=C(C1=CC=CC2=C1C=CC=C2)C3=NN(CCCCCF)C4=C3C=CC=C4
InChI Code1S/C23H21FN2O/c24-15-6-1-7-16-26-21-14-5-4-12-20(21)22(25-26)23(27)19-13-8-10-17-9-2-3-11-18(17)19/h2-5,8-14H,1,6-7,15-16H2
InChI KeyDULWRYKFTVFPTL-UHFFFAOYSA-N
WARNING - This product is not for human or veterinary use.
SHIPPING & STORAGE
Storage-20°C
ShippingRoom temperature in continental US; may vary elsewhere
StabilityAs supplied, 2 years from the QC date provided on the Certificate of Analysis, when stored properly

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Notice: This product is only suitable for laboratory use, or the use of animals. It can not be used directly on the human body

THJ-2201




THJ-2201 is an indazole-based synthetic cannabinoid that presumably acts as a potent
agonist of the CB1 receptor and has been sold online as a designer drug.
It is a structural analog of AM-2201 in which the central indole ring has been replaced by
indazole.
Cannabinoids are commonly smoked or vaporized to achieve a quick onset of effects and
rapid offset. THJ-2201 is orally active when dissolved in a lipid, which can increase the
duration significantly. Like other cannabinoids, it is insoluble in water but dissolves in
ethanol and lipids.
TECHNICAL INFORMATION
Formal Name[1-(5-fluoropentyl)-1H-indazol-3-yl]-1-naphthalenyl-methanone
CAS Number1801552-01-1
Synonyms
· AM2201 indazole analog
· 5-fluoropentyl JWH 018 indazole analog
· 5-fluoro THJ 018
Molecular FormulaC23H21FN2O
Formula Weight360.4
Purity≥98%
FormulationA crystalline solid
λmax219, 320 nm
SMILESO=C(C1=CC=CC2=C1C=CC=C2)C3=NN(CCCCCF)C4=C3C=CC=C4
InChI Code1S/C23H21FN2O/c24-15-6-1-7-16-26-21-14-5-4-12-20(21)22(25-26)23(27)19-13-8-10-17-9-2-3-11-18(17)19/h2-5,8-14H,1,6-7,15-16H2
InChI KeyDULWRYKFTVFPTL-UHFFFAOYSA-N
WARNING - This product is not for human or veterinary use.
SHIPPING & STORAGE
Storage-20°C
ShippingRoom temperature in continental US; may vary elsewhere
StabilityAs supplied, 2 years from the QC date provided on the Certificate of Analysis, when stored properly

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Notice: This product is only suitable for laboratory use, or the use of animals. It can not be used directly on the human body

4-Cl-PVP(crystal)





4-Cl-PVP(crystal) is a new research chemical act as a  psychostimulant.It is similar with a-PVP. Its purity is over 99.3%.
There is very little information regarding the pharmacology of 4-Cl-PVP(crystal) within the scientific literature. So it is available for sale as a grey area research chemical through Best-feel.com.
Detailed Description:
Product name: 4-cl-PVP
Molecular Formula: C15H20ClNO
Purity: Above 99.5%
Appearance: white crystals powder
IUPAC.: 1-(4-chlorophenyl)-2-(pyrrolidin-1-yl)pentan-1-one
Stock is available
1Product name4-Cl-PVP
2Full chemical name 1-(4-chlorophenyl)-2-(pyrrolidin-1-yl)pentan-1-one
3Formal Name 
4CAS numN/A
5Molecular Formula
C15H20ClNO
6 Average mass 265.78 g/mol
7Purity ≥99.2%
8Stability 2 years
9Storage -20°C
10Formulation A crystalline solid
11λmax 221, 315 nm
12Shipping Wet ice in continental US; may vary elsewhere

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arylcyclohexanamines


Arylcyclohexylamines, also known as arylcyclohexamines or arylcyclohexanamines, are a chemical class of pharmaceutical,designer, and experimental drugs.
General structure of arylcyclohexylamines
An arylcyclohexylamine is composed of a cyclohexylamine unit with an aryl moiety attachment. The aryl group is positioned geminal to theamine. In the simplest cases, the aryl moiety is typically a phenyl ring, sometimes with additional substitution. The amine is usually not primary, secondary amines such as methylamino or ethylamino, or tertiary cycloalkylamines such as piperidino and pyrrolidino, are the most commonly encountered N-substituents.

Pharmacology

Arylcyclohexylamines varyingly possess NMDA receptor antagonistic, dopamine reuptake inhibitory,and μ-opioid receptor agonistic properties. Additionally, σ receptor agonistic, nACh receptor antagonistic, and D2 receptor agonistic actions have been reported for some of these agents. Antagonism of the NMDA receptor confers anesthetic, anticonvulsant, neuroprotective, and dissociative effects; blockade of the dopamine transporter mediates stimulant and euphoriant effects as well as psychosis in high amounts; and activation of the μ-opioid receptor causes analgesic and euphoriant effects. Stimulation of the σ and D2 receptors may also contribute to hallucinogenic and psychomimetic effects.
Versatile agents with a wide range of possible pharmacological activities depending on the extent and range to which chemical modifications are implemented. The various choice of substitutions that are made allows for "fine-tuning" of the pharmacological profile that results. As examples, BTCP is a selectivedopamine reuptake inhibitor, PCP is primarily an NMDA antagonist, and BDPC is a superpotent μ-opioid agonist, while PRE-084 is a selective sigma receptor agonist. Thus, radically different pharmacology is possible through different structural combinations.

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2016年11月29日星期二

arylcyclohexamines


Arylcyclohexylamines, also known as arylcyclohexamines or arylcyclohexanamines, are a chemical class of pharmaceutical,designer, and experimental drugs.
General structure of arylcyclohexylamines
An arylcyclohexylamine is composed of a cyclohexylamine unit with an aryl moiety attachment. The aryl group is positioned geminal to theamine. In the simplest cases, the aryl moiety is typically a phenyl ring, sometimes with additional substitution. The amine is usually not primary, secondary amines such as methylamino or ethylamino, or tertiary cycloalkylamines such as piperidino and pyrrolidino, are the most commonly encountered N-substituents.

Pharmacology

Arylcyclohexylamines varyingly possess NMDA receptor antagonistic, dopamine reuptake inhibitory,and μ-opioid receptor agonistic properties. Additionally, σ receptor agonistic, nACh receptor antagonistic, and D2 receptor agonistic actions have been reported for some of these agents. Antagonism of the NMDA receptor confers anesthetic, anticonvulsant, neuroprotective, and dissociative effects; blockade of the dopamine transporter mediates stimulant and euphoriant effects as well as psychosis in high amounts; and activation of the μ-opioid receptor causes analgesic and euphoriant effects. Stimulation of the σ and D2 receptors may also contribute to hallucinogenic and psychomimetic effects.
Versatile agents with a wide range of possible pharmacological activities depending on the extent and range to which chemical modifications are implemented. The various choice of substitutions that are made allows for "fine-tuning" of the pharmacological profile that results. As examples, BTCP is a selectivedopamine reuptake inhibitor, PCP is primarily an NMDA antagonist, and BDPC is a superpotent μ-opioid agonist, while PRE-084 is a selective sigma receptor agonist. Thus, radically different pharmacology is possible through different structural combinations.

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Notice: This product is only suitable for laboratory use, or the use of animals. It can not be used directly on the human body

Arylcyclohexylamines


Arylcyclohexylamines, also known as arylcyclohexamines or arylcyclohexanamines, are a chemical class of pharmaceutical,designer, and experimental drugs.
General structure of arylcyclohexylamines
An arylcyclohexylamine is composed of a cyclohexylamine unit with an aryl moiety attachment. The aryl group is positioned geminal to theamine. In the simplest cases, the aryl moiety is typically a phenyl ring, sometimes with additional substitution. The amine is usually not primary, secondary amines such as methylamino or ethylamino, or tertiary cycloalkylamines such as piperidino and pyrrolidino, are the most commonly encountered N-substituents.

Pharmacology

Arylcyclohexylamines varyingly possess NMDA receptor antagonistic, dopamine reuptake inhibitory,and μ-opioid receptor agonistic properties. Additionally, σ receptor agonistic, nACh receptor antagonistic, and D2 receptor agonistic actions have been reported for some of these agents. Antagonism of the NMDA receptor confers anesthetic, anticonvulsant, neuroprotective, and dissociative effects; blockade of the dopamine transporter mediates stimulant and euphoriant effects as well as psychosis in high amounts; and activation of the μ-opioid receptor causes analgesic and euphoriant effects. Stimulation of the σ and D2 receptors may also contribute to hallucinogenic and psychomimetic effects.
Versatile agents with a wide range of possible pharmacological activities depending on the extent and range to which chemical modifications are implemented. The various choice of substitutions that are made allows for "fine-tuning" of the pharmacological profile that results. As examples, BTCP is a selectivedopamine reuptake inhibitor, PCP is primarily an NMDA antagonist, and BDPC is a superpotent μ-opioid agonist, while PRE-084 is a selective sigma receptor agonist. Thus, radically different pharmacology is possible through different structural combinations.

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Notice: This product is only suitable for laboratory use, or the use of animals. It can not be used directly on the human body

Phenacetin

Phenacetin (or acetophenetidin) is a pain-relieving and fever-reducing drug, which was widely used between its introduction in 1887 and the 1983 ban imposed by the FDA on its use in the United States. Its use has declined because of its adverse effects, which include increased risk of certain cancers and kidney damage. It is metabolized as paracetamol (acetaminophen), which replaced it in some over-the-counter medications following the ban on phenacetin.
Product Name: Phenacetin
Synonyms: 1-ACETYL-P-PHENETIDIN;4-ACETOPHENETIDIDE;4-acetophenetidine;4'-ETHOXYACETANILIDE;4-ETHOXYACETANILIDE;ACETOPHENETIDIN;ACETOPHENETIDINE;ACET-P-PHENETIDINE
CAS: 62-44-2
MF: C10H13NO2
MW: 179.22
EINECS: 200-533-0
Product Categories: Organics;Amines;Aromatics;Intermediates & Fine Chemicals;Pharmaceuticals;Other APIs
mp 133-136 °C(lit.)
bp 132 °C / 4mmHg
storage temp. 2-8°C
form powder
Water Solubility 0.076 g/100 mL
Sensitive Hygroscopic
Merck 14,7204
BRN 1869238
Stability: Stable. Incompatible with strong oxidizing agents, strong acids.
Chemical Properties : white crystalline powder
Usage : Analgesic, antipyretic. Component of APC tablets, analgesic mixture also containing aspirin and caffeine. Phenacetin is reasonably anticipated to be a human carcinogen; analgesic mixtures containing Phenacetin are listed as known human carcinogens.

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daturine


Hyoscyamine (also known as daturine) is a tropane alkaloid. It is a secondary metabolite found in certain plants of the family Solanaceae, including henbane (Hyoscyamus niger), mandrake (Mandragora officinarum), jimsonweed (Datura stramonium), tomato (Solanum lycopersicum) and deadly nightshade (Atropa belladonna). It is the levorotary isomer of atropine (third of the three major nightshade alkaloids) and thus sometimes known as levo-atropine. Hyoscyamine should not be confused with hyoscine, an older alternate name for the related nightshade-derived anticholinergic scopolamine for which it is the precursor.
Analysis
ANALYSISSPECIFICATIONRESULTS
AppearanceBrown powderComplies
OdorCharacteristicComplies
Assay (HPLC)≥0.8%0. 85%
Sieve analysis100% pass 80 meshComplies
Loss on Drying≤5.0%3.15%
Ash≤5.0%2.15%
Heavy Metal  
Pb<2ppmComplies
As<2ppmComplies
Hg<2ppmComplies
Residual SolventEur.PharmComplies
Microbiology 
Total Plate Count<1000cfu/gComplies
Yeast & Moulds<100cfu/gComplies
E.ColiNegativeComplies
SalmonellaNegativeComplies
SalmonellaNegativeComplies
Our advantages:
A.This raw material must be GMO free, 100% natural, Allergen free.
B.The capacity of extracting 1000 tons of different raw materials annually
C.GMP standard production line
D.Effective R&D work team
E.Modernized, rigorous and innovative management
Application:
A.Nutritional supplements
B.Health food products
C.Beverages
D.Pharmaceutical products
E.Skin Care Materials
Remark:
1)    Delivery: By UPS/DHL/TNT/EMS or By Air/Sea as QTY.
2)    Samples: Within 48 hours.
3)    Retail is accepted, Agent is welcome.

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Notice: This product is only suitable for laboratory use, or the use of animals. It can not be used directly on the human body

Hyoscyamine

Hyoscyamine (also known as daturine) is a tropane alkaloid. It is a secondary metabolite found in certain plants of the family Solanaceae, including henbane (Hyoscyamus niger), mandrake (Mandragora officinarum), jimsonweed (Datura stramonium), tomato (Solanum lycopersicum) and deadly nightshade (Atropa belladonna). It is the levorotary isomer of atropine (third of the three major nightshade alkaloids) and thus sometimes known as levo-atropine. Hyoscyamine should not be confused with hyoscine, an older alternate name for the related nightshade-derived anticholinergic scopolamine for which it is the precursor.
Analysis
ANALYSISSPECIFICATIONRESULTS
AppearanceBrown powderComplies
OdorCharacteristicComplies
Assay (HPLC)≥0.8%0. 85%
Sieve analysis100% pass 80 meshComplies
Loss on Drying≤5.0%3.15%
Ash≤5.0%2.15%
Heavy Metal
Pb<2ppmComplies
As<2ppmComplies
Hg<2ppmComplies
Residual SolventEur.PharmComplies
Microbiology
Total Plate Count<1000cfu/gComplies
Yeast & Moulds<100cfu/gComplies
E.ColiNegativeComplies
SalmonellaNegativeComplies
SalmonellaNegativeComplies
Our advantages:
A.This raw material must be GMO free, 100% natural, Allergen free.
B.The capacity of extracting 1000 tons of different raw materials annually
C.GMP standard production line
D.Effective R&D work team
E.Modernized, rigorous and innovative management
Application:
A.Nutritional supplements
B.Health food products
C.Beverages
D.Pharmaceutical products
E.Skin Care Materials
Remark:
1)    Delivery: By UPS/DHL/TNT/EMS or By Air/Sea as QTY.
2)    Samples: Within 48 hours.
3)    Retail is accepted, Agent is welcome.

my contact information is: 

Email: bettyapi1989@yahoo.com

Skype: bettyapi1989

Notice: This product is only suitable for laboratory use, or the use of animals. It can not be used directly on the human body