L-(-)-Ephedrine
- Product Name
- L-(-)-Ephedrine
- CAS No.
- 492-41-1
- Chemical Name
- L-(-)-Ephedrine
- Synonyms
- usafcs-6;Mydriatin;USAF cs-6;Propadrine;AURORA KA-7792;AURORA KA-7791;DL-NOREPHEDRINE;L-(-)-Ephedrine;(-)-norephedrin;(-)-benzylalcoho
- CBNumber
- CB2159410
- Molecular Formula
- C9H13NO
- Formula Weight
- 151.21
- MOL File
- 492-41-1.mol
L-(-)-Ephedrine Property
- Melting point:
- 51-53 °C(lit.)
- alpha
- -41 º (c=7, 1M HCl)
- Boiling point:
- 273.23°C (rough estimate)
- Density
- 1.0406 (rough estimate)
- refractive index
- 1.5380 (estimate)
- Flash point:
- >230 °F
- storage temp.
- 2-8°C
- form
- A solid
- pka
- 9.958(at 10℃)
- Stability:
- Stable. Incompatible with strong oxidizing agents. May discolour on exposure to light.
- CAS DataBase Reference
- 492-41-1(CAS DataBase Reference)
- NIST Chemistry Reference
- Phenylpropanolamine(492-41-1)
- EPA Substance Registry System
- Benzenemethanol, .alpha.-[(1S)-1-aminoethyl]-, (.alpha.R)- (492-41-1)
Safety
- Hazard Codes
- Xn
- Risk Statements
- 22-36/37/38
- Safety Statements
- 26
- WGK Germany
- 3
- RTECS
- RC2275000
- F
- 3-8-10
- Hazard Note
- Harmful
- Toxicity
- LD50 orl-rat: 1538 mg/kg BCFAAI 109,132,70
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H302Harmful if swallowed
H315Causes skin irritation
H319Causes serious eye irritation
H335May cause respiratory irritation
- Precautionary statements
-
P261Avoid breathing dust/fume/gas/mist/vapours/spray.
P264Wash hands thoroughly after handling.
P264Wash skin thouroughly after handling.
P270Do not eat, drink or smoke when using this product.
P301+P312IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.
P302+P352IF ON SKIN: wash with plenty of soap and water.
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
N-Bromosuccinimide Price
- Product number
- MT-20274
- Product name
- (1R,2S)-(-)-Norephedrine
- Purity
- 99%
- Packaging
- 250g
- Price
- $638
- Updated
- 2021/12/16
L-(-)-Ephedrine Chemical Properties,Usage,Production
Description
This alkaloid was first isolated by Kanao from the Chinese drug 'Ma-Huang'
(Ephedra sinica Stapf.) and later by Wolfes from E. helvetica C. A. Meyer and E.
distachya Linn. It forms a crystalline mass and has [α] 20
D - 14.56° (EtOH).
Several crystalline salts and derivatives are known: the hydrochloride has m.p.
171-2°C; [α] 20
D- 33.27° (H20); the sulphate dihydrate, m.p. 285-6°C (dry,
dec.); [α] 28
D- 31.99° (H20); the aurichloride, m.p. 188°C; platinichloride, m.p.
221°C (dec.); (-)-hydrogen tartrate, m.p. about 160° after sintering at 130°C;
oxalate, m.p. 245°C (dec.) and the p-nitrobenzoyl derivative, m.p. 175-6°C;
[α] 28
D- 49.58° (CHCI3).
The (+)-form has m.p. 52°C; [α] 27
D + 14.76° (EtOH), yielding a hydro_x0002_chloride, m.p. 171-2°C; [α] 27
D + 33.4° (EtOH); sulphate dihydrate, m.p. 285-
6°C (dry, dec.); [α] 27
D+ 31.51 0 C (H20); aurichloride, m.p. 188°C (dec.) and
platinichloride, m.p. 221.5°C (dec.). The (±)-form crystallizes as colourless
plates from Et20, m.p. 104-5°C and also furnishes a series of crystalline salts
and derivatives.
Chemical Properties
white powder
Uses
A metabolite of Phenmetrazine.
Definition
ChEBI: (-)-norephedrine is an amphetamine that is propylbenzene substituted by a hydroxy group at position 1 and by an amino group at position 2 (the 1R,2S-stereoisomer). It is a plant alkaloid. It has a role as a plant metabolite. It is a member of amphetamines and a phenethylamine alkaloid.
Safety Profile
A human poison by ingestion. Poison experimentally by intravenous, subcutaneous, and intraperitoneal routes. Moderately toxic by an unspecified route. Human systemic effects by ingestion: sleep, increased pulse rate without blood pressure decrease, and chronic pulmonary edema or congestion, convulsions, headache, and blood pressure elevation. Used in production of drugs of abuse. When heated to decomposition it emits toxic fumes of NOx.
References
Kanao., Ber., 63,95 (1930) Wolfes., Arch. Pharrn., 268,87 (1930) Hey., J. Chern. Soc., 1232 (1930) Akabori, Momotani., J. Chern. Soc., Japan, 64, 608 (1943) Hoover, Hass., J. Org. Chern., 12,506 (1947)