Cyclobutylamine

Cyclobutylamine Structure
CAS No.
2516-34-9
Chemical Name:
Cyclobutylamine
Synonyms
Cyclobutanamine;AMINOCYCLOBUTANE;obutyL;AURORA KA-7608;CYCLOBUTYLAMINE;Ring-butylaMine;1-Cyclobutanamine;CyclobutylaMine 98%;Cyclobutylamine,98%;Cyclobutane-1-amine
CBNumber:
CB0134657
Molecular Formula:
C4H9N
Molecular Weight:
71.12
MOL File:
2516-34-9.mol
MSDS File:
SDS
Modify Date:
2024/8/8 18:06:34

Cyclobutylamine Properties

Melting point 133-135.5 °C(Solv: ligroine (8032-32-4); dichloromethane (75-09-2))
Boiling point 81.5 °C752 mm Hg(lit.)
Density 0.833 g/mL at 25 °C(lit.)
refractive index n20/D 1.437(lit.)
Flash point 24 °F
storage temp. 2-8°C
pka 10.80±0.20(Predicted)
form Liquid
color Clear colorless to light yellow
Water Solubility slightly soluble
Sensitive Hygroscopic
BRN 2069297
InChIKey KZZKOVLJUKWSKX-UHFFFAOYSA-N
CAS DataBase Reference 2516-34-9(CAS DataBase Reference)
NIST Chemistry Reference Cyclobutylamine(2516-34-9)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS02,GHS05
Signal word  Danger
Hazard statements  H225-H314
Precautionary statements  P210-P233-P240-P280-P303+P361+P353-P305+P351+P338
Hazard Codes  F,C,Xi
Risk Statements  11-34-20/21/22-36/37/38
Safety Statements  16-26-36/37/39-45-33-7/9
RIDADR  UN 2733 3/PG 2
WGK Germany  3
HazardClass  3
PackingGroup  II
HS Code  29213000
NFPA 704
3
3 1

Cyclobutylamine price More Price(8)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) 225185 Cyclobutylamine 98% 2516-34-9 1G ₹4481.55 2022-06-14 Buy
Sigma-Aldrich(India) 225185 Cyclobutylamine 98% 2516-34-9 5G ₹22256.2 2022-06-14 Buy
Sigma-Aldrich(India) 225185 Cyclobutylamine 98% 2516-34-9 25G ₹75201.28 2022-06-14 Buy
ALFA India ALF-A13423-14 Cyclobutylamine, 98% 2516-34-9 25g ₹69543 2022-05-26 Buy
ALFA India ALF-A13423-06 Cyclobutylamine, 98% 2516-34-9 5g ₹13300 2022-05-26 Buy
Product number Packaging Price Buy
225185 1G ₹4481.55 Buy
225185 5G ₹22256.2 Buy
225185 25G ₹75201.28 Buy
ALF-A13423-14 25g ₹69543 Buy
ALF-A13423-06 5g ₹13300 Buy

Cyclobutylamine Chemical Properties,Uses,Production

Chemical Properties

Clear colorless to light yellow liquid

Uses

Cyclobutylamine is a substrate employed in a microwave-assisted synthesis of 7-azaindoles from dihalopyridines. Also it is a reactant in the preparation of imidazo[1,2-b]pyridazine derivatives as selective and orally available Mps1 (TTK) kinase inhibitors.

Preparation

The preparation of cyclobutylamine from cyclobutanecarboxylic acid and hydrazoic acid has been reported previously. Cyclobutylamine has also been prepared by the Hofmann-type rearrangement of cyclobutanecarboxamide. More recently it has been prepared in 82–87% overall yield from cyclobutanecarboxamide by oxidative rearrangement with lead tetraacetate or iodosobenzene diacetate.
Synthesis of cyclobutylamine
Synthesis of cyclobutylamine

Purification Methods

It has been purified by steam distillation. The aqueous distillate (e.g. 2L) is acidified with 3N HCl (90mL) and evaporated to dryness in a vacuum. The hydrochloride is treated with a few mL of H2O, cooled in ice and a slush of KOH pellets ground in a little H2O is added slowly in portions and keeping the solution very cold. The amine separates as an oil from the strongly alkaline solution. The oil is collected, dried over solid KOH and distilled using a vacuum jacketed Vigreux column (p 11) and protected from CO2 using a soda lime tube. The fraction boiling at 79-83o is collected, dried over solid KOH for 2days and redistilled over a few pellets of KOH (b 80.5-81.5o). Best distil in a dry N2 atmosphere. The purity can be checked by GLC using a polyethylene glycol on Teflon column at 72o, 15 psi, flow rate of 102 mL/min of He. The sample can appear homogeneous but because of tailing it is not possible to tell if H2O is present. The NMR in CCl4 should show no signals less than 1 ppm from TMS. The hydrochloride has a multiplet at ca 1.5-2.6ppm (H 2,2,4,3,3,4,4), a quintet at 3.8 ppm (H 1) and a singlet at 4.75 for NH2 [Roberts & Chambers J Am Chem Soc 73 2509 1951]. The benzenesulfonamide has m 85-86o (from aqueous MeOH) and the benzoyl derivative has m 120.6-121.6o. [Roberts & Mazur J Am Chem Soc 73 2509 1951, Iffland et al. J Am Chem Soc 75 4044 1953, Werner & Casanova Jr Org Synth Coll Vol V 273 1973, Beilstein 12 IV 3.]

Cyclobutylamine Preparation Products And Raw materials

Global( 258)Suppliers
Supplier Tel Country ProdList Advantage Inquiry
BTC pharm India +918790379245 AndhraPradesh, India 1269 58 Inquiry
GLR Innovations +91 9891111994 New Delhi, India 4542 58 Inquiry
BTC pharm India +918790379245 Telangana, India 145 58 Inquiry
ALLCHEM LIFESCIENCE PVT. LTD +91 957 472 2211 New Delhi, India 322 58 Inquiry
A.J Chemicals 91-9810153283 New Delhi, India 6124 58 Inquiry
CLEARSYNTH LABS LTD. +91-22-45045900 Hyderabad, India 6351 58 Inquiry
TCI Chemicals (India) Pvt. Ltd. 1800 425 7889 New Delhi, India 6778 58 Inquiry
Alfa Aesar 1 800 209 7001 Maharashtra, India 6913 58 Inquiry
A. B. Enterprises +91-8048077585 Mumbai, India 1396 58 Inquiry
BTC Nantong Pharmaceuticals Technology Co.,Ltd +8618068193575 China 254 58 Inquiry
AURORA KA-7608 CYCLOBUTYLAMINE 1-Cyclobutanamine Cyclobutane-1-amine Cyclobutylamine,98% Ring-butylaMine CyclobutylaMine 98% Cyclobutylamine,Aminocyclobutane Cyclobutylamine (free state) Aminocyclobutane > obutyL AMINOCYCLOBUTANE Cyclobutanamine 2516-34-9 2561-34-9 C4H9N C4H7NH2 C4H9N1 AMINE Simple 4-Membered Ring Compounds Cyclobutanes & Cyclobutenes Organic Building Blocks Nitrogen Compounds C2 to C6 Amines Building Blocks Imidazoles ,Homopiperidines Cyclobutanes & Cyclobutenes Simple 4-Membered Ring Compounds cyclic compounds Amines and Anilines