Norephedrine, (.+/-.)-

• Formula: C₉H₁₃NO
• Molecular weight: 151.2056
• IUPAC Standard InChI: InChI=1S/C9H13NO/c1-7(10)9(11)8-5-3-2-4-6-8/h2-7,9,11H,10H2,1H3 Copy

  
• IUPAC Standard InChIKey: DLNKOYKMWOXYQA-UHFFFAOYSA-N Copy
• CAS Registry Number: 14838-15-4
• Chemical structure:
  This structure is also available as a 2d Mol file
• Species with the same structure:
  • Benzenemethanol, α-(1-aminoethyl)-
• Stereoisomers:
  • (1S,2R)-(+)-Norephedrine
  • Cathine
  • (-)-Norephedrine
• Other names: Benzenemethanol, α-(1-aminoethyl)-, (R*,S*)-(.+/-.)-; (.+/-.)-Norephedrine; (.+/-.)-Phenylpropanolamine; Phenylpropanolamine; Propadrine; Phenylpropropanolamine; 2-Amino-1-phenyl-1-propanol; Benzyl alcohol, α-(1-amino-ethyl); DL-α-(1-aminoethyl)benzyl alcohol; DL-α-hydroxy-β-aminopropylbenzene; DL-Norephedrine; DL-1-Phenyl-2-aminopropanol-1; DL-2-Amino-1-hydroxy-1-phenylpropane; Mucron; Norephedrine; Rhindecon; dl-Propadrine; (.+/-.)-Norephedrin; dl-Phenylpropanolamine; (.+/-.)-α-(1-Aminoethyl)benzenemethanol; (1RS,2SR)-2-Amino-1-phenylpropan-1-ol; Phenylpropanolamine (.+/-.)-form; erythro-2-Amino-1-phenyl-1-propanol; NSC 9920; Super Odrinex; (R*,S*)-(±)-α-(1-aminoethyl)benzyl alcohol; (±) 2-Amino-1-phenyl-1-propanol (norephedrine)
• Information on this page:
  • Phase change data
  • Gas Chromatography
  • References
  • Notes
• Other data available:
  • Mass spectrum (electron ionization)
• Options:
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Phase change data

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Data compiled by: William E. Acree, Jr., James S. Chickos

Enthalpy of fusion

Gas Chromatography

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Data compiled by: NIST Mass Spectrometry Data Center, William E. Wallace, director

Kovats' RI, non-polar column, isothermal

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Kovats' RI, polar column, isothermal

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Normal alkane RI, non-polar column, temperature ramp

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References

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Li, Zell, et al., 1999
Li, Z. Jane; Zell, Mark T.; Munson, Eric J.; Grant, David J.W., Characterization of racemic species of chiral drugs using thermal analysis, thermodynamic calculation, and structural studies, J. Pharm. Sci., 1999, 88, 3, 337-346, https://doi.org/10.1021/js980205u . [all data]

Donike and Stratmann, 1976
Donike, M.; Stratmann, D., Gas-chromatographische identifizierung von stimulantien der phenyläthylaminreihe mit hilfe der retnetions-indices, Z. Anal. Chem., 1976, 279, 2, 129-131, https://doi.org/10.1007/BF00440798 . [all data]

Yashiki, Kojima, et al., 1995
Yashiki, M.; Kojima, T.; Miyazaki, T.; Nagasawa, N.; Iwasaki, Y.; Hara, K., Detection of amphetamines in urine using head space-solid phase microextraction and chemical ionization selected ion monitoring, Forensic Sci. Int., 1995, 76, 3, 169-177, https://doi.org/10.1016/0379-0738(95)01819-0 . [all data]

Marozzi, Gambaro, et al., 1982
Marozzi, E.; Gambaro, V.; Saligari, E.; Mariani, R.; Lodi, F., Use of the retention index in gas chromatographic studies of drugs, J. Anal. Toxicol., 1982, 6, 4, 185-192, https://doi.org/10.1093/jat/6.4.185 . [all data]

Notes

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• Symbols used in this document:
  

  ΔfusH

  Enthalpy of fusion

• Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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