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3721-28-6

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Basic Information
CAS No.: 3721-28-6
Name: TRANSAMINE
Article Data: 25
Molecular Structure:
Molecular Structure of 3721-28-6 (TRANSAMINE)
Formula: C9H11 N
Molecular Weight: 133.193
Synonyms: Cyclopropanamine,2-phenyl-, (1S-trans)-; ((1S,2R)-2-Phenylcyclopropyl)amine;(+)-Tranylcypromine; (+)-trans-2-Phenylcyclopropylamine;(1S,2R)-2-Phenylcyclopropanamine; (1S,2R)-Tranylcypromine;(1S-trans)-2-Phenylcyclopropylamine; 1-(S)-Amino-2-(R)-phenylcyclopropane;d-Tranylcypromine
Density: g/cm3
Boiling Point: 218.3°Cat760mmHg
Flash Point: 90.8°C
Risk Codes: R36/37/38; R25; R20/21
Safety: Poison by ingestion, intraperitoneal, and subcutaneous routes. Experimental reproductive effects. Mutation data reported. When heated to decomposition it emits toxic fumes of NOx. See also AMINES.
PSA: 26.02000
LogP: 2.20150
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Chemistry

IUPAC Name: (1R,2S)-2-Phenylcyclopropan-1-amine 
Molecular Formula: C9H11N
Molecular Weight: 133.21
Boiling Point: 218.3°C at 760mmHg
Flash Point: 90.8°C 
Freely Rotating Bonds: 2
Polar Surface Area: 3.24 Å2
Enthalpy of Vaporization: 45.47 kJ/mol
Vapour Pressure: 0.127 mmHg at 25°C 
Properties: white to light beige powder or chunks
The Cas Register Number  of trans-2-Phenylcyclopropylamine is 3721-28-6.The chemical synonyms of trans-2-Phenylcyclopropylamine (CAS NO.3721-28-6) are (+)-Tranylcypromine ; (1S,2R)-2-Phenylcyclopropanamine hydrochloride (1:1) ; (1S,2R)-2-phenylcyclopropanaminium chloride ; Cyclopropanamine, 2-phenyl-, (1S,2R)-, hydrochloride (1:1) ; d-Tranylcypromine ; trans-2-Phenylcyclopropylamine ; (+/-) - 2-Phenyl-cyclopropyl-ammonium ; (+/-) - 2-Phenyl-cyclopropyl-ammonium; chloride(Tranylcypromine ; hydrochloride) ; Chloride(Tranylcypromine ; Cyclopropanamine, 2-Phenyl-, trans-(+)- ; Hydrochloride) ; Tranylcypromine hydrochloride  .The molecular structure of trans-2-Phenylcyclopropylamine (CAS NO.3721-28-6) is.

Uses

 trans-2-Phenylcyclopropylamine (CAS NO.3721-28-6) is used as non-selective MAO-A/B inhibitor.

Toxicity Data With Reference

1.    

cyt-oin-urn 10 g/L

     JCLBA3    Journal of Cell Biology. 47 (1970),182a.
2.    

ipr-rat LD50:30 mg/kg

     FCTXAV    Food and Cosmetics Toxicology. 3 (1965),597.
3.    

orl-mus LD50:20 mg/kg

     BCPCA6    Biochemical Pharmacology. 17 (1968),369.
4.    

ipr-mus LD50:11,300 µg/kg

     BRXXAA    British Patent Document. (U.S. Patent Office, Science Library, 2021 Jefferson Davis Highway, Arlington, VA 22202) #1460700 .
5.    

scu-mus LD50:30 mg/kg

     BCPCA6    Biochemical Pharmacology. 17 (1968),369.

Safety Profile

Poison by ingestion, intraperitoneal, and subcutaneous routes. Experimental reproductive effects. Mutation data reported. When heated to decomposition it emits toxic fumes of NOx. See also AMINES.
Hazard Codes: ToxicT
Risk Statements: 36/37/38-25-20/21 
R36/37/38: Irritating to eyes, respiratory system and skin. 
R25: Toxic if swallowed. 
R20/21: Harmful by inhalation and in contact with skin.
Safety Statements: 45-36/37/39-26 
S45: In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.) 
S36/37/39: Wear suitable protective clothing, gloves and eye/face protection. 
S26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
RIDADR: 3249
WGK Germany: 3
HazardClass: 6.1(b)
PackingGroup: III

Specification

  trans-2-Phenylcyclopropylamine (CAS NO.3721-28-6) was found to be both an inhibitor and a substrate of lysyl oxidase, the enzyme which oxidizes peptidyl lysine in elastin and collagen to initiate cross-linking in these proteins.