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DL-α-(Aminomethyl)-p-hydroxybenzylalkoholhydrochlorid

DL-Octopamine hydrochloride  Struktur
770-05-8
CAS-Nr.
770-05-8
Bezeichnung:
DL-α-(Aminomethyl)-p-hydroxybenzylalkoholhydrochlorid
Englisch Name:
DL-Octopamine hydrochloride
Synonyma:
OCTOPAMINE HCL;OCTOPAMINE HYDROCHLORIDE;dl-octopamine;OCTAPAMINE HCL;OCTOPAMINE HCL(P);OCTOPAMINE HCL(RG);DL-Octopaminehydroc;(+,-)-Octopamine HCl;OctopaMine HCl 99%Min;Chapter hydrochloride
CBNumber:
CB8778718
Summenformel:
C8H12ClNO2
Molgewicht:
189.64
MOL-Datei:
770-05-8.mol

DL-α-(Aminomethyl)-p-hydroxybenzylalkoholhydrochlorid Eigenschaften

Schmelzpunkt:
~170 °C (dec.)(lit.)
Siedepunkt:
290℃[at 101 325 Pa]
Dichte
1.39[at 20℃]
Dampfdruck
0.002Pa at 20℃
storage temp. 
2-8°C
L?slichkeit
H2O: soluble
Aggregatzustand
solid
Farbe
white or off-white
Wasserl?slichkeit
soluble
Merck 
13,6791
BRN 
3915414
Stabilit?t:
Stable.
LogP
-2.6 at 20.1℃
CAS Datenbank
770-05-8(CAS DataBase Reference)

Sicherheit

Kennzeichnung gef?hrlicher Xn,Xi
R-S?tze: 20/21/22-36/37/38
S-S?tze: 36-37/39-26
RIDADR  3249
WGK Germany  3
HazardClass  6.1(b)
PackingGroup  III

DL-α-(Aminomethyl)-p-hydroxybenzylalkoholhydrochlorid Chemische Eigenschaften,Einsatz,Produktion Methoden

R-S?tze Betriebsanweisung:

R20/21/22:Gesundheitssch?dlich beim Einatmen,Verschlucken und Berührung mit der Haut.
R36/37/38:Reizt die Augen, die Atmungsorgane und die Haut.

S-S?tze Betriebsanweisung:

S36:DE: Bei der Arbeit geeignete Schutzkleidung tragen.
S37/39:Bei der Arbeit geeignete Schutzhandschuhe und Schutzbrille/Gesichtsschutz tragen.
S26:Bei Berührung mit den Augen sofort gründlich mit Wasser abspülen und Arzt konsultieren.

Chemische Eigenschaften

DL-Octopamine hydrochloride is a light-yellow crystalline solid and derived from the dried young fruit of Citrus aurantium L., a plant of the Rutaceae family,It is soluble to 10 mg/ml in PBS, 10 mg/ml in EtOH, and 12 mg/ml in DMSO & DMF. Its use is similar to that of Synflorin HCL. It is an adrenergic alpha-receptor stimulant with vasoconstrictive and hypertensive effects.

Verwenden

A biogenic amine that is the phenol analog of Noradrenaline. It is a neurosecretory product found in several vertebrates and invertebrates. Adrenergic.

Biologische Aktivit?t

Invertebrate biogenic amine neurotransmitter, related to noradrenalin, that is an adrenoceptor agonist. Stimulates lipolysis in mammalian adipocytes via activation of β 3 receptors. Has dual effect on glucose transport in adipocytes: inhibits transport via β 3 receptor activation but stimulates transport when oxidised by MAO. Also activates human α 2A receptors, inhibiting subsequent cAMP production.

Mode of action

Octopamine hydrochloride is an invertebrate biogenic amine neurotransmitter, related to noradrenalin, that is an adrenoceptor (AR) agonist. Octopamine hydrochloride stimulates lipolysis in mammalian adipocytes via activation of β3-AR receptors. Has dual effect on glucose transport in adipocytes: inhibits transport via β3-AR receptor activation but stimulates transport when oxidised by MAO. Also activates human α2A-AR receptors, inhibiting subsequent cAMP production.

DL-α-(Aminomethyl)-p-hydroxybenzylalkoholhydrochlorid Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


DL-α-(Aminomethyl)-p-hydroxybenzylalkoholhydrochlorid Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.

Global( 385)Lieferanten
Firmenname Telefon E-Mail Land Produktkatalog Edge Rate
Hebei Weibang Biotechnology Co., Ltd
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Hebei Mojin Biotechnology Co., Ltd
+86 13288715578 +8613288715578
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+86-13131129325
sales1@chuanghaibio.com China 5889 58
BINBO BIOLOGICAL CO.,LTD
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info@tnjchem.com China 2986 55
career henan chemical co
+86-0371-86658258 +8613203830695
sales@coreychem.com China 29880 58

770-05-8(DL-α-(Aminomethyl)-p-hydroxybenzylalkoholhydrochlorid)Verwandte Suche:


  • OCTOPAMINE HCL(RG)
  • Octopamine hydrochloride 99.0%min
  • α-(Aminomethyl)-4-hydroxybenzyl alcohol hydrochloride, (±)-1-(4-Hydroxyphenyl)-2-aminoethanol hydrochloride
  • 4-(2-Amino-1-hydroxyethyl)phenol hydrochloride
  • alpha-(Aminomethyl)-p-hydroxybenzylic alcohol hydrochloride
  • DL-Octopamine hydrochloride,98+%
  • (±)-Octopamine hydrochloride,α-(Aminomethyl)-4-hydroxybenzyl alcohol hydrochloride, (±)-1-(4-Hydroxyphenyl)-2-amino-ethanol hydrochloride
  • (+/-)-p-OctopaMaine-Hydrochloride
  • (+)p-octopaMine hydrochloride
  • (±)-p-OctopaMine-a,,-d3 HCl
  • (±)-para-Octopamine (hydrochloride)
  • (±)-1-(4-Hydroxyphenyl)-2-amino
  • DL-Octopamine hydrochloride≥ 99% (HPLC,anhydrous basis)
  • OctopaMine HCl 99%Min
  • ChapteraMine hydrochloride
  • Chapter hydrochloride
  • OctopaMinehydrochlorid
  • Benzenemethanol, .alpha.-(aminomethyl)-4-hydroxy-, hydrochloride, (.+-.)-
  • Benzyl alcohol, .alpha.-(aminomethyl)-p-hydroxy-, hydrochloride, (.+-.)-
  • dl-Epirenor hydrochlor
  • DL-OCTOPAMINE HYDROCHLORIDE
  • DL-1-(4-HYDROXYPHENYL)-2-AMINOETHANOL HYDROCHLORIDE
  • dl-alpha-(aminomethyl)-4-hydroxybenzyl alcohol hydrochloride
  • DL-A-(AMINOMETHYL)-P-HYDROXYBENZYL ALCOHOL HYDROCHLORIDE
  • 1-[P-HYDROXYPHENYL]-2-AMINOETHANOL HCL
  • 1-[P-HYDROXYPHENYL]-2-AMINOETHANOL HYDROCHLORIDE
  • (+/-)-1-(4-HYDROXYPHENYL)-2-AMINOETHANOL HYDROCHLORIDE
  • OCTAPAMINE HCL
  • (+/-)-OCTOPAMINE HYDROCHLORIDE
  • P-(+/-)-ALPHA-(AMINOMETHYL)HYDROXYBENZYL ALCOHOL, HCL
  • P-HYDROXYPHENYLAMINOETHANOL HYDROCHLORIDE
  • ALPHA-(AMINOMETHYL)-4-HYDROXYBENZENEMETHANOL HYDROCHLORIDE
  • DL-alpha-(aminomethyl)-p-hydroxybenzylic alcohol hydrochloride
  • Octopamine(Norsynephrine)
  • DL-Octapamine hydrochloride.
  • OCTOPAMINE HCL(P)
  • DL-Octopaminehydroc
  • (+,-)-Octopamine HCl
  • alpha-(Aminomethyl)-4-hydroxybenzyl Alcohol Hydrochloride
  • DL-Octopamine hydrochloride USP/EP/BP
  • (±)-p-Octopamine hydrochlorid
  • OCTOPAMINE HYDROCHLORIDE
  • OCTOPAMINE HCL
  • dl-octopamine
  • 2H4]-(±)-Octopamine hydrochloride salt
  • (+/-)-Octopamine hydrochloride analytical standard, ≥98%
  • (±)-Octopamine hydrochloride in Methanol
  • 770-05-8
  • C8H11NO2xHCl
  • C8H11NO2HClC8H12ClNO2
  • alpha-adrenoceptor agonist; invertebrate neurotransmitter.
  • Building Blocks
  • Amino Alcohols
  • Oxygen Compounds
  • Organic Building Blocks
  • Pharma raw material
  • Amines
  • Aromatics
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