Buy article online - an online subscription or single-article purchase is required to access this article.
Download citation
Download citation
link to html
The title molecule, C12H18O3, crystallized in the centrosymmetric space group P21/c with two molecules in the asymmetric unit. Each molecule donates three, and accepts three, hydrogen bonds. The Od...Oa distances in these bonds range from 2.687 (3) to 2.787 (2) Å. The hydroxyl H atoms are ordered. A three-dimensional network of hydrogen-bond chains is formed which is `decorated' with sets of cyclic hydrogen bonds and numerous finite hydrogen-bond patterns. This structure shows both similarities and differences with respect to the structures of the related molecules benzene-1,3,5-triacetic acid and benzene-1,3,5-trimethanol.

Supporting information

cif

Crystallographic Information File (CIF)
Contains datablocks global, fg1397

hkl

Structure factor file (CIF format)
Contains datablock fg1397

CCDC reference: 130074

-1

Subscribe to Acta Crystallographica Section C: Structural Chemistry

The full text of this article is available to subscribers to the journal.

If you have already registered and are using a computer listed in your registration details, please email support@iucr.org for assistance.

Buy online

You may purchase this article in PDF and/or HTML formats. For purchasers in the European Community who do not have a VAT number, VAT will be added at the local rate. Payments to the IUCr are handled by WorldPay, who will accept payment by credit card in several currencies. To purchase the article, please complete the form below (fields marked * are required), and then click on `Continue'.
E-mail address* 
Repeat e-mail address* 
(for error checking) 

Format*   PDF (US $40)
In order for VAT to be shown for your country javascript needs to be enabled.

VAT number 
(non-UK EC countries only) 
Country* 
 

Terms and conditions of use
Contact us

Follow Acta Cryst. C
Sign up for e-alerts
Follow Acta Cryst. on Twitter
Follow us on facebook
Sign up for RSS feeds