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420290

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IPTG, Hemidioxane Adduct

A free-flowing, hygroscopic carbohydrate that induces expression of the lac operon of E. coli by allosterically interacting with the repressor molecule.

Synonym(s):
IPTG, Hemidioxane Adduct, Isopropyl-β-D-thiogalactopyranoside
Empirical Formula (Hill Notation):
C9H18O5S · 0.5C4H8O2
CAS Number:
Molecular Weight:
282.35
MDL number:

Quality Level

Assay

≥98% (HPLC)

form

solid

manufacturer/tradename

Calbiochem®

storage condition

OK to freeze
desiccated (hygroscopic)

impurities

15.0% dioxane

color

white to off-white

solubility

water: 1%
ethanol: soluble

shipped in

ambient

storage temp.

2-8°C

InChI

1S/C9H18O5S/c1-4(2)15-9-8(13)7(12)6(11)5(3-10)14-9/h4-13H,3H2,1-2H3/t5-,6+,7+,8-,9+/m1/s1

InChI key

BPHPUYQFMNQIOC-NXRLNHOXSA-N

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This Item
I1284420291IPTG-RO
Millipore

Millipore

420290

IPTG, Hemidioxane Adduct

form

solid

form

liquid

form

solid

form

powder

manufacturer/tradename

Calbiochem®

manufacturer/tradename

-

manufacturer/tradename

Calbiochem®

manufacturer/tradename

Roche

storage condition

OK to freeze, desiccated (hygroscopic)

storage condition

-

storage condition

OK to freeze, desiccated (hygroscopic)

storage condition

-

color

white to off-white

color

-

color

white to off-white

color

-

solubility

water: 1%, ethanol: soluble

solubility

-

solubility

water: 100 mg/mL, methanol: soluble

solubility

-

General description

A free flowing carbohydrate that induces expression of the lac operon of E. coli by allosterically interacting with the repressor molecule. Inducer of β-D-galactosidase.
A free-flowing, hygroscopic carbohydrate that induces expression of the lac operon of E. coli by allosterically interacting with the repressor molecule. Inducer of β-D-galactosidase. This preparation contains 15% dioxane.

Warning

Toxicity: Carcinogenic / Teratogenic (D)

Reconstitution

Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 6 months at -20°C.

Other Notes

Mathur, A., et al. 2000. Cardiovasc. Res. 46, 126.
Chanda, B., and Mathew, M.K. 1999. Biochim Biophys. Acta 1416, 92.
Dedov, V.N., and Roufogalis, B.D. 1999. FEBS Lett. 456, 171.
Polla, B.S., et al. 1996. Proc. Natl. Acad. Sci. USA 93, 6458.
White, R.J., et al. 1996. J. Neurosci. 16, 5688.
Ankacrona, M., et al. 1995. Neuron 15, 961.
Reers, M., et al. 1995. Methods Enzymol. 260, 406.
Ravanello, M.P., and Kruby, D.E. 1994. J. Virol.68, 6401.
Schmitz, M.L., and Baeurerle, P.A. 1994. Biotechniques17, 714.
Cossarizza, A., et al. 1993. Biochem. Biophys. Res. Commun. 197, 40.
Lama, J., et al. 1992. Gene117, 185.
Zhang, Y., and Moss, B. 1991. Proc. Natl. Acad. Sci. USA88, 1511.
Rodriquez, J.F., and Smith, G.L. 1990. Nucleic Acids Res.18, 5347.
Date, T., et al. 1988. Biochem. Biophys. Res. Commun.151, 598.
Lee, S.G., et al. 1988. Biochemistry27, 2983.
Cho, S., et al. 1985. Biochem. Biophys. Res. Commun.128, 1268.

Legal Information

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


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