Basic information Safety Supplier Related

(S)-1-(4-Nitrophenyl)ethylamine hydrochloride

Basic information Safety Supplier Related

(S)-1-(4-Nitrophenyl)ethylamine hydrochloride Basic information

Product Name:
(S)-1-(4-Nitrophenyl)ethylamine hydrochloride
Synonyms:
  • METHYL-4-NITROBENZYLAMINEHYDROCHLORIDE
  • (R)-4-Nitro-α-methylbenzylamine hydrochloride
  • Benzenemethanamine, .alpha.-methyl-4-nitro-, monohydrochloride, (.alpha.R)-
  • (r)-α-methyl-4-nitrobenzylamine hydrochloride
  • (R)-A-METHYL-4-NITROBENZYLAMINE HYDROCHLORIDE,97%
  • (R)-(-)-1-(4-NITROPHENYL)-ETHYLAMINE HCL
  • (R)-1-(4-NITROPHENYL)ETHYLAMINE HYDROCHLORIDE
  • (R)-4-NITROPHENYL-1-ETHYLAMINE HYDROCHLORIDE
CAS:
57233-86-0
MF:
C8H11ClN2O2
MW:
202.64
Mol File:
57233-86-0.mol
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(S)-1-(4-Nitrophenyl)ethylamine hydrochloride Chemical Properties

Melting point:
248-250 °C(lit.)
alpha 
-6.5 º (c=1, 0.05N NaOH)
storage temp. 
Inert atmosphere,Room Temperature
optical activity
[α]25/D +6.0°, c = 1 in 0.05 M NaOH
BRN 
3701567
CAS DataBase Reference
57233-86-0(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-37/39
WGK Germany 
3
3-10

MSDS

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(S)-1-(4-Nitrophenyl)ethylamine hydrochloride Usage And Synthesis

Purification Methods

To ensure dryness, the hydrochloride (ca 175 g) is extracted with EtOH (3x100mL) and evaporated to dryness (any residual H2O increases the solubility in EtOH and lowers the yield). The hydrochloride residue is triturated with absolute EtOH and dried in vacuo. The product is further purified by refluxing with absolute EtOH (200 mL for 83g) for 1hour, and cool to 10o to give 76.6g of hydrochloride m 243-245o(dec). The free base is prepared by dissolving in N NaOH, extracting with CH2Cl2 (3 x 500mL), drying (Na2CO3), filtering, evaporating and distilling it. It has m 27o, b 119-120o/0.5mm (105-107o/0.5mm, 157-159o/9mm, d 1.1764, n 1.5688, [] ±17.7o (neat) [Perry et al. Synthesis 492 1977,ORD: Nerdel & Liebig Justus Liebigs Ann Chem 621 142 1959]. [Beilstein 12 IV 2451.]

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