Merck
  • 27602
All Photos(1)

27602

Sigma-Aldrich

Caffeine

anhydrous, tested according to Ph. Eur.

Synonym(s):
Coffeinum, 1,3,7-Trimethylxanthine
Empirical Formula (Hill Notation):
C8H10N4O2
CAS Number:
Molecular Weight:
194.19
Beilstein:
17705
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.21

grade

anhydrous

Quality Level

Agency

EPA 1694
USP/NF
tested according to Ph. Eur.

form

powder

mp

234-236.5 °C (lit.)

solubility

H2O: soluble 18.7 g/L at 16 °C

application(s)

environmental

SMILES string

CN1C(=O)N(C)c2ncn(C)c2C1=O

InChI

1S/C8H10N4O2/c1-10-4-9-6-5(10)7(13)12(3)8(14)11(6)2/h4H,1-3H3

InChI key

RYYVLZVUVIJVGH-UHFFFAOYSA-N

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This Item
1085003BP766C7731
Caffeine anhydrous, tested according to Ph. Eur.

Sigma-Aldrich

27602

Caffeine

Caffeine United States Pharmacopeia (USP) Reference Standard

USP

1085003

Caffeine

Caffeine British Pharmacopoeia (BP) Reference Standard

BP766

Caffeine

Caffeine meets USP testing specifications, anhydrous

Sigma-Aldrich

C7731

Caffeine

grade

anhydrous

grade

pharmaceutical primary standard

grade

pharmaceutical primary standard

grade

anhydrous

agency

EPA 1694, USP/NF, tested according to Ph. Eur.

agency

-

agency

-

agency

USP/NF, meets USP testing specifications

mp

234-236.5 °C (lit.)

mp

234-236.5 °C (lit.)

mp

234-236.5 °C (lit.)

mp

234-236.5 °C (lit.)

form

powder

form

-

form

-

form

crystalline, powder

solubility

H2O: soluble 18.7 g/L at 16 °C

solubility

-

solubility

-

solubility

H2O: soluble 18.7 g/L at 16 °C

application(s)

environmental

application(s)

pharmaceutical (small molecule)

application(s)

-

application(s)

-

Application

Caffeine has been used as a radiosensitizing agent utilized for studying its impact in inhibiting the catalytic activity of ATM and ATR Kinase. CTGF is an important modulator protein of fibrogenic TGF-β. Hence, this product has also been used for examining the caffeine-dependent regulation of CTGF expression in rat hepatocytes.

Biochem/physiol Actions

A central nervous system stimulant believed to act through adenosine receptors and monoamine neurotransmitters. It is an adenosine receptor antagonist and adenosine 3′,5′-cyclic monophosphate (cAMP) phosphodiesterase inhibitor. Thus, levels of cAMP increase in cells following treatment with caffeine. It has been reported to affect cellular calcium levels, releasing calcium from intracellular stores. It overrides the cell cycle effects of various chemicals such as protease inhibitors, preventing apoptosis; and it has been shown to inhibit cellular DNA repair mechanisms.
Caffeine is a central nervous system stimulant, adenosine receptor antagonist as well as adenosine 3′,5′-cyclic monophosphate (cAMP) phosphodiesterase inhibitor. It stimulates the sarcoplasmic reticulum (SR) Ca2+-release channel which facilitates the excitation-contraction coupling in cardiac muscle. It has also been reported to affect cellular calcium levels, releasing calcium from intracellular stores. Caffeine overrides the cell cycle effects of various chemicals such as protease inhibitors, preventing apoptosis; and it has been shown to inhibit cellular DNA repair mechanisms.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Precautionary Statements

Hazard Classifications

Acute Tox. 4 Oral

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificate of Analysis

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Certificate of Origin

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