Chemodex

Yohimbine hydrochloride

Product Code:
 
CDX-Y0013
Product Group:
 
Other Biochemicals
Supplier:
 
Chemodex
Regulatory Status:
 
RUO
Shipping:
 
Ambient
Storage:
 
+4°C
1 / 1
Chemical Structure

Chemical Structure

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CodeSizePrice
CDX-Y0013-G0055 g£78.00
Quantity:
CDX-Y0013-G02525 g£280.00
Quantity:
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This product comes from: Switzerland.
Typical lead time: 7-10 working days.
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Further Information

Alternate Names/Synonyms:
17-Hydroxyyohimban-16-carboxylic acid methyl ester hydrochloride; Actibine; Antagonil; Aphrodyne; Dayto-Himbin; Erex; NIH 9689; NSC19509; Thybine
Appearance:
White to off-white powder.
CAS:
65-19-0
Class:
6.1
EClass:
32160000
Form (Short):
liquid
GHS Symbol:
GHS06
Handling Advice:
Keep cool and dry.Protect from light and moisture.
Hazards:
H300, H311, H331
InChi:
InChI=1S/C21H26N2O3.ClH/c1-26-21(25)19-15-10-17-20-14(13-4-2-3-5-16(13)22-20)8-9-23(17)11-12(15)6-7-18(19)24;/h2-5,12,15,17-19,22,24H,6-11H2,1H3;1H/t12-,15-,17-,18-,19+;/m0./s1
InChiKey:
PIPZGJSEDRMUAW-VJDCAHTMSA-N
Long Description:
Chemical. CAS: 65-19-0. Formula: C21H26N2O3 . HCl. MW: 354.4 . 36.5. Synthetic. alpha2-Adrenoceptor antagonist. pKi values are 8.52, 8.00 and 9.17 for human alpha2A, alpha2B and alpha2C receptors, respectively.
MDL:
MFCD00012674
Molecular Formula:
C21H26N2O3 . HCl
Molecular Weight:
354.4 . 36.5
Package Type:
Vial
PG:
II
Precautions:
P261, P264, P280, P301, P310, P311
Product Description:
alpha2-Adrenoceptor antagonist. pKi values are 8.52, 8.00 and 9.17 for human alpha2A, alpha2B and alpha2C receptors, respectively. Selective adenosine A2A-receptor antagonist.
Purity:
>98% (TLC)
Signal word:
Danger
SMILES:
O[C@@H]1[C@H](C(OC)=O)[C@](C2)([H])[C@](CC1)([H])CN(CC3)[C@]2([H])C4=C3C(C=CC=C5)=C5N4.Cl
Solubility Chemicals:
Soluble in water (10mg/ml).
Source / Host:
Synthetic.
Transportation:
Excepted Quantity
UN Nummer:
1544PSN2
UNSPSC Category:
Biochemical Reagents
UNSPSC Number:
12352200
Use & Stability:
Stable for at least 2 years after receipt when stored at -20°C.

References

(1) M.R. Goldberg & D. Robertson; Pharmacol. Rev. 35, 143 (1983) | (2) W.S. Redfern & A. Williams; Br. J. Pharmacol. 116, 2081 (1995) | (3) S.G. Lalchandani, et al.; JPET 303, 979 (2002) | (4) P. Lahiri, et al.; Platelets 16, 111 (2005)