ContaminantDB: (cis)-crotonaldehyde

Identification Taxonomy Biological Properties Physical Properties Toxicity Profile Spectra Concentrations Links References XML

Record Information

Version

1.0

Creation Date

2016-05-27 01:41:11 UTC

Update Date

2016-11-09 01:22:32 UTC

Accession Number

CHEM041755

Identification

Common Name

(cis)-crotonaldehyde

Class

Small Molecule

Description

Not Available

Contaminant Sources

FooDB Chemicals

Contaminant Type

Not Available

Chemical Structure

MOL SDF PDB SMILES InChI

Synonyms

Value	Source
(2E)-2-Butenal	HMDB
(2E)-But-2-enal	HMDB
(2Z)-2-Butenal	HMDB
(cis)-Crotonaldehyde	HMDB
(e)-But-2-enal	HMDB
(e)-Crotonaldehyde	HMDB
(e)-Crotonaldehyde (iupac)	HMDB
(Z)-2-Butenal	HMDB
(Z)-Crotonaldehyde	HMDB
1-Formylpropene	HMDB
2-Butenal	HMDB
2-BUTENAL (trans) crotonaldehyde	HMDB
2-Butenal, inhibited	HMDB
2-Butenal, mixture OF cis and trans	HMDB
2-Butenaldehyde	HMDB
3-Methylacrolein, inhibited	HMDB
Aldehyde crotonique	HMDB
beta-Methyl acrolein	HMDB
beta-Methylacrolein	HMDB
But-(e)-2-enal	HMDB
But-2-enal	HMDB
cis-Crotonaldehyde	HMDB
CRD	HMDB
Crotenaldehyde	HMDB
Crotonal	HMDB
Crotonaldehyde	HMDB
Crotonaldehyde, inhibited	HMDB
Crotonaldehyde, mixture OF cis and trans	HMDB
Crotonaldehyde, predominantly trans	HMDB
Crotonaldehyde, stabilized	HMDB
Crotonic aldehyde	HMDB
Crotylaldehyde	HMDB
e-2-Butenal	HMDB
Krotonaldehyd	HMDB
Methylpropenal	HMDB
Nchem.215-comp8	HMDB
t-2-Butenal	HMDB
Topanel	HMDB
Topanel ca	HMDB
trans- Crotonal	HMDB
trans-2-Butenal	HMDB
trans-Crotonaldehyde	HMDB

Chemical Formula

C₄H₆O

Average Molecular Mass

70.090 g/mol

Monoisotopic Mass

70.042 g/mol

CAS Registry Number

Not Available

IUPAC Name

(2Z)-but-2-enal

Traditional Name

crotonaldehyde

SMILES

C\C=C/C=O

InChI Identifier

InChI=1S/C4H6O/c1-2-3-4-5/h2-4H,1H3/b3-2-

InChI Key

MLUCVPSAIODCQM-IHWYPQMZSA-N

Chemical Taxonomy

Description

belongs to the class of organic compounds known as enals. These are an alpha,beta-unsaturated aldehyde of general formula RC=C-CH=O in which the aldehydic C=O function is conjugated to a C=C triple bond at the alpha,beta position.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbonyl compounds

Direct Parent

Enals

Alternative Parents

Substituents

Enal
Organic oxide
Hydrocarbon derivative
Short-chain aldehyde
Aldehyde
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

Not Available

Biological Properties

Status

Detected and Not Quantified

Origin

Not Available

Cellular Locations

Not Available

Biofluid Locations

Not Available

Tissue Locations

Not Available

Pathways

Not Available

Applications

Not Available

Biological Roles

Not Available

Chemical Roles

Not Available

Physical Properties

State

Not Available

Appearance

Not Available

Experimental Properties

Property	Value
Melting Point	Not Available
Boiling Point	Not Available
Solubility	Not Available

Predicted Properties

Property	Value	Source
Water Solubility	66.5 g/L	ALOGPS
logP	0.88	ALOGPS
logP	0.76	ChemAxon
logS	-0.02	ALOGPS
pKa (Strongest Basic)	-4.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	17.07 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	22.04 m³·mol⁻¹	ChemAxon
Polarizability	7.52 Å³	ChemAxon
Number of Rings	0	ChemAxon
Bioavailability	1	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	Yes	ChemAxon
MDDR-like Rule	No	ChemAxon

Spectra

Spectrum Type	Description	Splash Key	View
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (Non-derivatized) - 70eV, Positive	splash10-00fu-9000000000-7ffbd3d633407bac8d5e	Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	splash10-00di-9000000000-08eccdf5cccaed87856c	Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	splash10-0fk9-9000000000-a3444f5bb9b35a780025	Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	splash10-0006-9000000000-812fdbefffebfdd9ca05	Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Negative	splash10-014i-9000000000-9b36a65bdeff1558f337	Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Negative	splash10-014l-9000000000-c8f8e709afcffd783260	Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Negative	splash10-0f6x-9000000000-7ffc09f4e2e3568ae093	Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	splash10-0uk9-9000000000-930b0e2bbb268b285753	Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	splash10-0udl-9000000000-b146ab174aebfe8f37a3	Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	splash10-0udi-9000000000-c512574bc7b38df158d4	Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Negative	splash10-014i-9000000000-1fe3e74f4451b5653b93	Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Negative	splash10-014i-9000000000-6a804ed7b9cae4dbf0cd	Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Negative	splash10-0f6x-9000000000-6eca02e73c31ee64da5f	Spectrum

Toxicity Profile

Route of Exposure

Not Available

Mechanism of Toxicity

Not Available

Metabolism

Not Available

Toxicity Values

Not Available

Lethal Dose

Not Available

Carcinogenicity (IARC Classification)

Not Available

Uses/Sources

Not Available

Minimum Risk Level

Not Available

Health Effects

Not Available

Symptoms

Not Available

Treatment

Not Available

Concentrations

Not Available

External Links

DrugBank ID

Not Available

HMDB ID

HMDB0303986

FooDB ID

FDB030138

Phenol Explorer ID

Not Available

KNApSAcK ID

Not Available

BiGG ID

Not Available

BioCyc ID

Not Available

METLIN ID

Not Available

PDB ID

Not Available

Wikipedia Link

Not Available

Chemspider ID

559039

ChEBI ID

Not Available

PubChem Compound ID

Not Available

Kegg Compound ID

Not Available

YMDB ID

Not Available

ECMDB ID

Not Available

References

Synthesis Reference

Not Available

MSDS

Not Available

General References

Not Available

(cis)-crotonaldehyde (CHEM041755)

Structure for CHEM041755: (cis)-crotonaldehyde