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Creatine

A carboxylic acid, C4H9N3O2, 131.135 g/mol. Melting point 255 dec °C, density 1.33 at 25 °C, as published.

verified record, Organic — carboxylic acid, 5 measured properties

Identifiers

Molecular formula
C₄H₉N₃O₂
Molecular weight
131.135 g/mol
Exact mass
131.069477 g/mol
IUPAC name
2-[carbamimidoyl(methyl)amino]acetic acid
SMILES
CN(CC(=O)O)C(=N)N
InChI
InChI=1S/C4H9N3O2/c1-7(4(5)6)2-3(8)9/h2H2,1H3,(H3,5,6)(H,8,9)
InChIKey
CVSVTCORWBXHQV-UHFFFAOYSA-N

Measured properties

Published measurements, each with its source. Two readings of one property are both shown, in the units each used.

Melting Point
255 dec °Cmeasured · DrugBank
Decomposes at 303 °Cmeasured · Hazardous Substances Data Bank (HSDB)
Density
1.33 at 25 °Cmeasured · Hazardous Substances Data Bank (HSDB)
Solubility
13300 mg/L (at 18 °C)measured · DrugBank
Slightly soluble in water, insoluble in ethermeasured · Hazardous Substances Data Bank (HSDB)
Vapor Pressure
0.00079 [mmHg]measured · Haz-Map, Information on Hazardous Chemicals and Occupational Diseases
LogP
-0.2measured · DrugBank

Calculated properties

Derived from the structure, not from a sample; kept apart from the measurements above.

Molecular weight
131.13 g/molcalculated · reference compound database
Average mass of one molecule, from reference compound database.
Exact mass
131.069476538 Dacalculated · reference compound database
Mass of the most common isotopic form.
XLogP3
-1.2calculated · reference compound database
Estimated oil/water partition, computed by reference compound database.
Polar surface area
90.4 Ųcalculated · reference compound database
Polar surface area as computed by reference compound database.
Complexity
134calculated · reference compound database
A rough measure of how intricate the structure is.
H-bond donors
3calculated · reference compound database
H-bond acceptors
3calculated · reference compound database
logP
-1.1037calculated · chemistry engine
Estimated preference for oil over water. Higher means more oil-like.
Topological polar surface area
90.41 Ųcalculated · chemistry engine
Surface area from polar atoms; relates to how easily a molecule crosses membranes.
H-bond donors
3calculated · chemistry engine
Atoms that can donate a hydrogen bond.
H-bond acceptors
2calculated · chemistry engine
Atoms that can accept a hydrogen bond.
Rotatable bonds
2calculated · chemistry engine
Single bonds the molecule can freely twist around.
Molar refractivity
32.1799 cm³/molcalculated · chemistry engine
Relates to the molecule's polarisability.
Fraction sp³ carbons
0.5calculated · chemistry engine
Share of carbon atoms with tetrahedral bonding.
QED drug-likeness
0.3274calculated · chemistry engine
Quantitative estimate of drug-likeness (0–1).

What it is made of

Elements

Percentages are of the molecular weight above, worked out the same way the molar mass calculator does it.

Structure

Heavy atoms, hydrogen excluded
9
Total atoms, hydrogen included
18
Rings
0
Aromatic rings
0
Stereocentres
0
Formal charge
0

Functional groups

  • Carboxylic acid

    A carbon double-bonded to oxygen and bonded to an –OH group; acidic.

Matched by structural pattern, not by a measurement.

The molecule in three dimensions

Rotate and inspect the atoms. Loaded only when you ask, so the page stays light.

The drawing above is a diagram of what is bonded to what. A molecule is not flat, and the model here is one low-energy shape generated from the connectivity — useful for seeing which groups can reach each other, and not a measured structure. A real sample is a population of conformations, interconverting.

Reactions it appears in

No documented reaction with a written procedure and a source involves Creatine yet.

Other names for it

The systematic name on this record is 2-[carbamimidoyl(methyl)amino]acetic acid.

The sources also call it Creatin, N-amidinosarcosine, Kreatin, Krebiozon, methylglycocyamine, N-methyl-N-guanylglycine, Glycine, N-(aminoiminomethyl)-N-methyl-, Pyrolysate, (alpha-Methylguanido)acetic acid, N-carbamimidoyl-N-methylglycine, Cosmocair C 100.

Structurally related

Nothing structurally close to Creatine has a page here yet.

Where these values came from

compound record.

What this page does not claim

Identifiers are copied from the source record, measured values are reported as published, and calculated values are marked as calculated. Nothing here is a hazard, purity or handling assessment — how the library is checked.