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SMB00209

Sigma-Aldrich

Nimbidiol

≥95% (LC/MS-ELSD)

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About This Item

Empirical Formula (Hill Notation):
C17H22O3
CAS Number:
Molecular Weight:
274.35
UNSPSC Code:
12352205
PubChem Substance ID:
NACRES:
NA.25

Pricing and availability is not currently available.

assay

≥95% (LC/MS-ELSD)

form

solid

application(s)

metabolomics
vitamins, nutraceuticals, and natural products

storage temp.

−20°C

SMILES string

CC1(C)CCC[C@@]2(C)C1CC(=O)c3cc(O)c(O)cc23

InChI

1S/C17H22O3/c1-16(2)5-4-6-17(3)11-8-14(20)13(19)7-10(11)12(18)9-15(16)17/h7-8,15,19-20H,4-6,9H2,1-3H3/t15?,17-/m1/s1

InChI key

JMBKXUYCBVKSSY-OMOCHNIRSA-N

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This Item
270768157120188247
assay

95%

assay

97%

assay

98%

assay

99%

Quality Level

100

Quality Level

200

Quality Level

100

Quality Level

100

density

0.928 g/mL at 25 °C (lit.)

density

1.236 g/mL at 25 °C (lit.)

density

1.007 g/mL at 25 °C (lit.)

density

1.159 g/mL at 25 °C (lit.)

refractive index

n20/D 1.517 (lit.)

refractive index

n20/D 1.545 (lit.)

refractive index

n20/D 1.536 (lit.)

refractive index

n20/D 1.559 (lit.)

bp

140 °C/20 mmHg (lit.)

bp

93-94 °C/1.5 mmHg (lit.)

bp

135 °C/20 mmHg (lit.)

bp

168-169 °C/2 mmHg (lit.)

form

liquid

form

liquid

form

liquid

form

liquid

General description

Natural product derived from plant source.
Nimbidiol is a modified diterpenoid. It is isolated from the root-bark of Azadirachta indica (Indian ‘neem′).[1]

Biochem/physiol Actions

Nimbidiol has an ability to inhibit intestinal glucosidases, including maltase-glucoamylase, sucrase-isomaltase, lactase, trehalase and fungal α-glucosidases. Thus, this bioactive molecule has all the potential to be used as an anti-diabetic drug [2]

pictograms

Exclamation markEnvironment

signalword

Warning

hcodes

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


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Chemical modification of copolyimides with bulky pendent groups: effect of modification on solubility and thermal stability.
Maya EM, et al.
Polymer Degradation and Stability, 92(12), 2294-2299 (2007)
The crystal structure of the inclusion complex of cyclomaltoheptaose (?-cyclodextrin) with 4-tert-butylbenzoic acid.
Rontoyianni A, et al.
Carbohydrate Research, 252, 19-32 (1994)
The selective oxidation of benzyl alcohols in a membrane reactor.
Grigoropoulou G, et al.
Chemical Communications (Cambridge, England), 6, 547-548 (2001)
Tsunehisa Hirose et al.
Molecules (Basel, Switzerland), 24(13) (2019-07-05)
The retention behavior of a wide variety of stationary phases was compared in supercritical fluid chromatography (SFC) and normal-phase high-performance liquid chromatography (NP-HPLC). We also attempted to elucidate the retention behavior in SFC by investigating the selectivity of the different

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