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Cyclopropylamine

Cyclopropylamine Suppliers list
Company Name: Shandong Vantage Specialty Chemicals Biotechnology Co., Ltd.  Gold
Tel: 13396369453 18678026865
Email: sdfantai@163.com
Company Name: Shandong Xibang Biological Technology Development Co. LTD  Gold
Tel: 0536-3611186 15063661551
Email: 196056703@qq.com
Company Name: Shandong Qianyuan Polymer Material Co. , Ltd.  Gold
Tel: 18678041314 18765609661
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Company Name: Weifang Mingran Chemical Co., Ltd.  Gold
Tel: QQ117761326 QQ2829453795 15063661899;
Email: mingranchem@163.com
Company Name: J & K SCIENTIFIC LTD.  
Tel: 18210857532 18210857532
Email: jkinfo@jkchemical.com

Cyclopropylamine manufacturers

  • Cyclopropylamine
  • Cyclopropylamine pictures
  • $10.00
  • 2026-05-28
  • CAS:765-30-0
  • Min. Order: 1KG
  • Purity: 95%
  • Supply Ability: 10 ton
  • Cyclopropylamine
  • Cyclopropylamine pictures
  • $490.00
  • 2025-04-09
  • CAS:765-30-0
  • Purity: 99 %
  • Supply Ability: 500 Kg
Cyclopropylamine Basic information
Product Name:Cyclopropylamine
Synonyms:CYCLOPROPYLAMINE;AURORA KA-2551;AKOS BBS-00003593;AMINOTRIMETHYLENE;Cyloprolylamine;Cyclopropyl amine(CPA);Cydopropylamine;Cyclopropylamine,98%
CAS:765-30-0
MF:C3H7N
MW:57.09
EINECS:212-142-2
Product Categories:Pharmaceutical Intermediates;Cyclopropanes;Simple 3-Membered Ring Compounds
Mol File:765-30-0.mol
Cyclopropylamine Structure
Cyclopropylamine Chemical Properties
Melting point -50 °C
Boiling point 49-50 °C (lit.)
density 0.824 g/mL at 25 °C (lit.)
vapor pressure 4.67 psi ( 20 °C)
refractive index n20/D 1.420(lit.)
Fp −14 °F
storage temp. Store below +30°C.
solubility Chloroform, Ethyl Acetate (Sparingly), Methanol (Slightly)
form Volatile Liquid
pkapK1:9.10(+1) (25°C)
Specific Gravity0.824
color Clear colorless
Water Solubility Miscible with water, ethanol,ether and chloroform.
Specific Heat CapacityCp(liquid): 2.58 J/(g·K), at 25℃
Sensitive Lachrymatory
BRN 741858
Stability:Volatile
InChI1S/C3H7N/c4-3-1-2-3/h3H,1-2,4H2
InChIKeyHTJDQJBWANPRPF-UHFFFAOYSA-N
SMILESNC1CC1
LogP0.070
CAS DataBase Reference765-30-0(CAS DataBase Reference)
NIST Chemistry ReferenceCyclopropylamine(765-30-0)
EPA Substance Registry SystemCyclopropanamine (765-30-0)
Safety Information
Hazard Codes F,C,Xi
Risk Statements 11-22-34-36/37
Safety Statements 16-26-36/37/39-45-33-7/9
RIDADR UN 2733 3/PG 2
WGK Germany 2
RTECS GZ0685500
Autoignition Temperature527 °F
Hazard Note Extremely Flammable/Harmful/Corrosive/Lachrymatory
TSCA TSCA listed
HazardClass 3
PackingGroup II
HS Code 29213099
Storage Class3 - Flammable liquids
Hazard ClassificationsAcute Tox. 4 Oral
Flam. Liq. 2
Skin Corr. 1B
ToxicityLD50 orally in Rabbit: 445 mg/kg
MSDS Information
ProviderLanguage
Aminocyclopropane English
SigmaAldrich English
ACROS English
ALFA English
Cyclopropylamine Usage And Synthesis
Chemical PropertiesCyclopropylamine is a colorless and transparent flammable liquid with volatility and ammonia odor. It is miscible with water, methanol, ethanol, benzene, toluene and other solvents.
UsesCyclopropylamine is used in the preparation of N-[4-(4-fluoro)phenyl-2-aminothiazol-5-yl]pyrimidin-2-yl-alkylamine derivatives. It is also used to prepare Pt(CPA)2(bismethylthiomethylenepropanedioate) and Pt(CPA)2(bisethylthiomethylenepropanedioate) complexes.
DefinitionChEBI: Cyclopropylamine is a primary aliphatic amine that consists of cyclopropane bearing a single amino substituent. It has a role as a mouse metabolite.
ApplicationCyclopropylamine is mainly used in organic synthesis, pharmaceutical synthesis intermediates, and can be used in the synthesis of new antibacterial drugs ciprofloxacin products, such as the synthesis of ciprofloxacin, enrofloxacin, spafloxacin and other drugs. In addition, cyclopropylamine is also an important intermediate for the synthesis of pesticides, plant protection agents and herbicides, such as 2-chloro-4-6-cyclopropyl-s-triazine, cyprochlor, cyproterazine, cyprocyanine and other cyclopropanes class of pesticides.
PreparationCyclopropylamine is synthesized from 1,3-propanediol by bromination, cyanation, cyclization, amidation, and Hoffmann rearrangement. It is also synthesized with γ-butyrolactone and isopropanol by five steps of ring-opening esterification, cyclization, hydrolysis, acylation and Hofmann degradation.
Biochem/physiol ActionsCyclopropylamine inactivates cytochrome P450 enzymes by a mechanism involving initial one-electron oxidation at nitrogen followed by scission of the cyclopropane ring leading to covalent modification of the enzyme. It is a mechanism-based inhibitor of quinoprotein methylamine dehydrogenase from Paracoccus denitrificans.
Purification MethodsIt has been isolated as the benzamide m 100.6-101.0o (from aqueous EtOH). It forms a picrate m 149o (from EtOH/pet ether) from which the free base can be recovered using a basic ion-exchange resin and can then be distilled through a Todd column (p 11) using an automatic still head which only collects products boiling below 51o/atm. Polymeric materials if present will boil above this temperature. The hydrochloride has m 85-86o [Roberts & Chambers J Am Chem Soc 73 5030 1951, Jones J Org Chem 9 484 1944, Emmons J Am Chem Soc 79 6522 1957]. [Beilstein 12 IV 3.]
Tag:Cyclopropylamine(765-30-0) Related Product Information
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