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Safety Information

726796

Sigma-Aldrich

(S)-(+)-1-Cyclohexylethylamine

ChiPros®, produced by BASF, 99%

Synonym(s):

(S)-(+)-α-Methylcyclohexanemethylamine

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About This Item

Linear Formula:
C6H11CH(CH3)NH2
CAS Number:
17430-98-7
Molecular Weight:
127.23
Beilstein:
2935069
MDL number:
MFCD00066261
UNSPSC Code:
12352116
PubChem Substance ID:
329764266
NACRES:
NA.22

grade

produced by BASF

Quality Level

100

Assay

≥98.5% (GC)
99%

form

liquid

optical purity

enantiomeric excess: ≥98.5%

refractive index

n20/D 1.4614 (lit.)

bp

60 °C/12 mmHg (lit.)

density

0.856 g/mL at 25 °C (lit.)

functional group

amine

SMILES string

C[C@H](N)C1CCCCC1

InChI

1S/C8H17N/c1-7(9)8-5-3-2-4-6-8/h7-8H,2-6,9H2,1H3/t7-/m0/s1

InChI key

XBWOPGDJMAJJDG-ZETCQYMHSA-N

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General description

(S)-(+)-1-Cyclohexylethylamine is a chiral amine.

Application

(S)-(+)-1-Cyclohexylethylamine may be used in the synthesis of (S)-(-)-ferrocenylimine by reacting with ferrocenecarboxaldehyde.

Legal Information

ChiPros is a registered trademark of BASF SE

Signal Word

Danger

Hazard Statements

H226,H314,H411

Hazard Classifications

Aquatic Chronic 2 - Flam. Liq. 3 - Skin Corr. 1B

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

125.6 °F - closed cup

Flash Point(C)

52 °C - closed cup

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

FSL

Group 4: Flammable liquids
Type 2 petroleums
Hazardous rank III
Water insoluble liquid

JAN Code

726796-VAR:
726796-25G:
726796-BULK:
726796-100G:

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Certificates of Analysis (COA)

Lot/Batch Number
BCCG5492
BCCC5336
BCCB5072
BCBV5981
BCBP2349V

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Chiral mono and diamide derivatives of calix [4] arene for enantiomeric recognition of chiral amines
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Chirality, 20.1, 26-34 (2008)
Yee Voan Teo et al.
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Articles

ChiPros Chiral Amines

Chiral amines play an important role in stereoselective organic synthesis. They are used directly as resolving agents, building blocks, or chiral auxiliaries.

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