#------------------------------------------------------------------------------
#$Date: 2025-08-19 13:01:59 +0300 (Tue, 19 Aug 2025) $
#$Revision: 301802 $
#$URL: file:///home/coder/svn-repositories/cod/cif/2/10/85/2108580.cif $
#------------------------------------------------------------------------------
#
# This file is available in the Crystallography Open Database (COD),
# http://www.crystallography.net/. The original data for this entry
# were provided by IUCr Journals, http://journals.iucr.org/.
#
# The file may be used within the scientific community so long as
# proper attribution is given to the journal article from which the
# data were obtained.
#
data_2108580
loop_
_publ_author_name
'Patyk-Kaźmierczak, Ewa'
'Kaźmierczak, Michał'
_publ_section_title
;
 A new high-pressure benzocaine polymorph --- towards understanding the
 molecular aggregation in crystals of an important active pharmaceutical
 ingredient (API)
;
_journal_coeditor_code           LO5062SUP1
_journal_issue                   1
_journal_name_full               'Acta Crystallographica Section B'
_journal_page_first
;
;
_journal_paper_doi               10.1107/S2052520619016548
_journal_volume                  76
_journal_year                    2020
_chemical_formula_moiety         'C9 H11 N O2'
_chemical_formula_sum            'C9 H11 N O2'
_chemical_formula_weight         165.19
_chemical_name_common            Benzocaine
_chemical_name_systematic        '4-aminobenzoic acid ethyl ester'
_space_group_crystal_system      monoclinic
_space_group_IT_number           14
_space_group_name_Hall           '-P 2ybc'
_space_group_name_H-M_alt        'P 1 21/c 1'
_atom_sites_solution_hydrogens   mixed
_atom_sites_solution_primary     dual
_audit_creation_date             2019-03-18
_audit_creation_method
;
Olex2 1.2
(compiled 2018.05.29 svn.r3508 for OlexSys, GUI svn.r5506)
;
_cell_angle_alpha                90
_cell_angle_beta                 92.00(4)
_cell_angle_gamma                90
_cell_formula_units_Z            4
_cell_length_a                   8.171(13)
_cell_length_b                   5.3995(9)
_cell_length_c                   19.515(3)
_cell_measurement_reflns_used    704
_cell_measurement_temperature    298(2)
_cell_measurement_theta_max      19.5340
_cell_measurement_theta_min      3.8680
_cell_volume                     860.5(14)
_computing_cell_refinement       'CrysAlisPro 1.171.38.41 (Rigaku OD, 2015)'
_computing_data_collection       'CrysAlisPro 1.171.38.41 (Rigaku OD, 2015)'
_computing_data_reduction        'CrysAlisPro 1.171.38.41 (Rigaku OD, 2015)'
_computing_molecular_graphics    'Olex2 (Dolomanov et al., 2009)'
_computing_publication_material  'Olex2 (Dolomanov et al., 2009)'
_computing_structure_refinement  'ShelXL (Sheldrick, 2015)'
_computing_structure_solution    'ShelXT (Sheldrick, 2015)'
_diffrn_ambient_temperature      298(2)
_diffrn_detector                 'CCD plate'
_diffrn_detector_area_resol_mean 16.1544
_diffrn_detector_type            Eos
_diffrn_measured_fraction_theta_full 0.278
_diffrn_measured_fraction_theta_max 0.248
_diffrn_measurement_details
;
List of Runs (angles in degrees, time in seconds):

  # Type    Start    End  Width  tₑₓₚ   ω     θ     κ     φ   Frames
--------------------------------------------------------------------------
  1  φ    -35.00  19.75   0.75   32.00   0.00 -30.00   0.00    --    73
  2  φ    140.00 200.00   0.75   32.00   0.00 -30.00   0.00    --    80
  3  φ    160.00 217.00   0.75   32.00   0.00  30.00   0.00    --    76
  4  φ    -20.00  34.75   0.75   32.00   0.00  30.00   0.00    --    73
  5  ω    -24.00  24.00   0.75   32.00    --   30.00  39.46 -12.90   64
  6  ω    -24.00  24.00   0.75   32.00    --   30.00  39.46 167.10   64
  7  ω    -50.00  10.00   0.75   32.00    --  -30.00  39.46 167.10   80
  8  ω    -50.00  10.00   0.75   32.00    --  -30.00  39.46 -12.90   80
  9  ω    -64.00  -8.50   0.75   32.00    --  -30.00  81.40 -28.90   74
 10  ω    -64.00  -8.50   0.75   32.00    --  -30.00  81.40 151.10   74
 11  ω    -19.00   8.00   0.75   32.00    --   30.00  81.40 151.10   36
 12  ω    -19.00   8.00   0.75   32.00    --   30.00  81.40 -28.90   36
 13  ω    -43.00 -21.25   0.75   32.00    --   30.00 134.60 -56.90   29
 14  ω    -43.00 -21.25   0.75   32.00    --   30.00 134.60 123.10   29
 15  ω    -90.00 -36.00   0.75   32.00    --  -30.00 134.60 123.10   72
 16  ω    -90.00 -36.00   0.75   32.00    --  -30.00 134.60 -56.90   72
;
_diffrn_measurement_device       'four-circle diffractometer'
_diffrn_measurement_device_type  'Xcalibur, Eos'
_diffrn_measurement_method       'ω and φ scans'
_diffrn_orient_matrix_type
'CrysAlisPro convention (1999,Acta A55,543-557)'
_diffrn_orient_matrix_UB_11      0.0855371000
_diffrn_orient_matrix_UB_12      -0.0242629000
_diffrn_orient_matrix_UB_13      -0.0002352000
_diffrn_orient_matrix_UB_21      -0.0162766000
_diffrn_orient_matrix_UB_22      -0.1275193000
_diffrn_orient_matrix_UB_23      -0.0052067000
_diffrn_orient_matrix_UB_31      -0.0008699000
_diffrn_orient_matrix_UB_32      0.0184628000
_diffrn_orient_matrix_UB_33      -0.0359671000
_diffrn_radiation_monochromator  graphite
_diffrn_radiation_probe          x-ray
_diffrn_radiation_type           MoK\a
_diffrn_radiation_wavelength     0.71073
_diffrn_reflns_av_R_equivalents  0.0690
_diffrn_reflns_av_unetI/netI     0.0425
_diffrn_reflns_Laue_measured_fraction_full 0.278
_diffrn_reflns_Laue_measured_fraction_max 0.248
_diffrn_reflns_limit_h_max       2
_diffrn_reflns_limit_h_min       -2
_diffrn_reflns_limit_k_max       6
_diffrn_reflns_limit_k_min       -6
_diffrn_reflns_limit_l_max       24
_diffrn_reflns_limit_l_min       -24
_diffrn_reflns_number            3571
_diffrn_reflns_point_group_measured_fraction_full 0.278
_diffrn_reflns_point_group_measured_fraction_max 0.248
_diffrn_reflns_theta_full        25.242
_diffrn_reflns_theta_max         26.935
_diffrn_reflns_theta_min         3.916
_diffrn_source                   'fine-focus sealed X-ray tube'
_diffrn_source_type              'Enhance (Mo) X-ray Source'
_exptl_absorpt_coefficient_mu    0.091
_exptl_absorpt_correction_T_max  1.00000
_exptl_absorpt_correction_T_min  0.52626
_exptl_absorpt_correction_type   multi-scan
_exptl_absorpt_process_details
;
CrysAlisPro 1.171.38.41 (Rigaku Oxford Diffraction, 2015)
Empirical absorption correction using spherical harmonics,
 implemented in SCALE3 ABSPACK scaling algorithm.
;
_exptl_crystal_colour            colourless
_exptl_crystal_colour_primary    colourless
_exptl_crystal_density_diffrn    1.275
_exptl_crystal_description       plate
_exptl_crystal_F_000             352
_exptl_crystal_recrystallization_method
; Crystal grown at high-pressure in diamond-anvil cell from 97.5% DMSO 
solution in water, at 0.41 GPa
;
_exptl_crystal_size_max          0.34
_exptl_crystal_size_mid          0.29
_exptl_crystal_size_min          0.1
_refine_diff_density_max         0.136
_refine_diff_density_min         -0.150
_refine_diff_density_rms         0.039
_refine_ls_extinction_method     none
_refine_ls_goodness_of_fit_ref   1.102
_refine_ls_hydrogen_treatment    constr
_refine_ls_matrix_type           full
_refine_ls_number_parameters     99
_refine_ls_number_reflns         462
_refine_ls_number_restraints     133
_refine_ls_restrained_S_all      0.986
_refine_ls_R_factor_all          0.1521
_refine_ls_R_factor_gt           0.0867
_refine_ls_shift/su_max          0.000
_refine_ls_shift/su_mean         0.000
_refine_ls_structure_factor_coef Fsqd
_refine_ls_weighting_details
'w=1/[σ²(Fo²)+(0.1481P)²] where P=(Fo²+2Fc²)/3'
_refine_ls_weighting_scheme      calc
_refine_ls_wR_factor_gt          0.2331
_refine_ls_wR_factor_ref         0.2772
_reflns_Friedel_coverage         0.000
_reflns_number_gt                228
_reflns_number_total             462
_reflns_threshold_expression     'I > 2σ(I)'
_cod_data_source_file            lo5062sup1.cif
_cod_data_source_block           BZC_b1
_cod_original_cell_volume        860.4(14)
_cod_database_code               2108580
_cod_database_fobs_code          2108580
_shelx_shelxl_version_number     2014/7
_chemical_oxdiff_formula         C9H11O2N1
_shelx_space_group_comment
;
The symmetry employed for this shelxl refinement is uniquely defined
by the following loop, which should always be used as a source of
symmetry information in preference to the above space-group names.
They are only intended as comments.
;
_shelx_estimated_absorpt_t_max   0.991
_shelx_estimated_absorpt_t_min   0.970
_reflns_odcompleteness_completeness 23.10
_reflns_odcompleteness_iscentric 1
_reflns_odcompleteness_theta     27.91
_olex2_refinement_description
;
1. Fixed Uiso
 At 1.2 times of:
  All C(H) groups, All C(H,H) groups, All N(H,H) groups
 At 1.5 times of:
  All C(H,H,H) groups
2. Restrained distances
 C4-C7
 1.5 with sigma of 0.02
3. Uiso/Uaniso restraints and constraints
C1 \\sim C2 \\sim C4 \\sim C3 \\sim C5 \\sim C6 \\sim C7: within 2A with sigma
of 0.01 and sigma for terminal atoms of 0.02
C7 \\sim O2 \\sim C8: within 2A with sigma of 0.01 and sigma for terminal atoms
of 0.02
C8 \\sim C9: within 2A with sigma of 0.02 and sigma for terminal atoms of 0.04
Uanis(C1) \\sim Ueq, Uanis(N1) \\sim Ueq, Uanis(C2) \\sim Ueq, Uanis(C3) \\sim
Ueq, Uanis(C4) \\sim Ueq, Uanis(C5) \\sim Ueq, Uanis(C6) \\sim Ueq, Uanis(C7)
\\sim Ueq, Uanis(O1) \\sim Ueq, Uanis(O2) \\sim Ueq, Uanis(C8) \\sim Ueq,
Uanis(C9) \\sim Ueq: with sigma of 0.05 and sigma for terminal atoms of 0.1
4.a Rotating group:
 N1(H1A,H1B)
4.b Secondary CH2 refined with riding coordinates:
 C8(H8A,H8B)
4.c Aromatic/amide H refined with riding coordinates:
 C3(H3), C2(H2), C6(H6), C5(H5)
4.d Fitted hexagon refined as free rotating group:
 C4(C3,C2,C1,C6,C5)
4.e Idealised Me refined as rotating group:
 C9(H9A,H9B,H9C)
;
_olex2_exptl_crystal_mounting_method
'Crystal mounted in diamond-anvil cell at 0.41 GPa'
_olex2_submission_special_instructions 'No special instructions were received'
_oxdiff_exptl_absorpt_empirical_details
;
Empirical correction (ABSPACK) includes:
- Absorption correction using spherical harmonics
- Frame scaling
;
_oxdiff_exptl_absorpt_empirical_full_max 2.140
_oxdiff_exptl_absorpt_empirical_full_min 0.493
loop_
_space_group_symop_operation_xyz
'x, y, z'
'-x, y+1/2, -z+1/2'
'-x, -y, -z'
'x, -y-1/2, z-1/2'
loop_
_atom_site_label
_atom_site_type_symbol
_atom_site_fract_x
_atom_site_fract_y
_atom_site_fract_z
_atom_site_U_iso_or_equiv
_atom_site_adp_type
_atom_site_occupancy
_atom_site_site_symmetry_order
_atom_site_calc_flag
_atom_site_refinement_flags_posn
_atom_site_refinement_flags_adp
O1 O 0.222(3) 0.4071(13) 0.1341(4) 0.104(14) Uani 1 1 d . U
O2 O 0.368(2) 0.6836(10) 0.0748(3) 0.107(6) Uani 1 1 d . U
N1 N 0.972(3) 0.1295(11) 0.2035(4) 0.104(15) Uani 1 1 d . U
H1A H 1.0479 0.1668 0.1745 0.125 Uiso 1 1 d GR .
H1B H 0.9735 -0.0328 0.2080 0.125 Uiso 1 1 d GR .
C4 C 0.5207(16) 0.3999(9) 0.1405(3) 0.086(7) Uani 1 1 d D U
C3 C 0.6624(17) 0.5218(8) 0.1219(2) 0.087(7) Uani 1 1 d G U
H3 H 0.6551 0.6642 0.0952 0.104 Uiso 1 1 calc R .
C2 C 0.8148(16) 0.4307(10) 0.1433(3) 0.091(7) Uani 1 1 d G U
H2 H 0.9096 0.5122 0.1309 0.109 Uiso 1 1 calc R .
C1 C 0.8257(16) 0.2178(11) 0.1832(3) 0.087(7) Uani 1 1 d G U
C6 C 0.6841(16) 0.0959(8) 0.2018(2) 0.090(7) Uani 1 1 d G U
H6 H 0.6914 -0.0466 0.2285 0.108 Uiso 1 1 calc R .
C5 C 0.5316(16) 0.1870(8) 0.1804(3) 0.086(7) Uani 1 1 d G U
H5 H 0.4369 0.1054 0.1928 0.104 Uiso 1 1 calc R .
C7 C 0.354(3) 0.490(2) 0.1176(6) 0.091(7) Uani 1 1 d D U
C9 C 0.245(3) 0.9909(14) -0.0004(4) 0.131(11) Uani 1 1 d . U
H9A H 0.2915 0.9206 -0.0404 0.197 Uiso 1 1 calc GR .
H9B H 0.3207 1.1064 0.0205 0.197 Uiso 1 1 calc GR .
H9C H 0.1449 1.0751 -0.0132 0.197 Uiso 1 1 calc GR .
C8 C 0.209(3) 0.7854(17) 0.0505(5) 0.111(7) Uani 1 1 d . U
H8A H 0.1496 0.8510 0.0887 0.133 Uiso 1 1 calc R .
H8B H 0.1430 0.6571 0.0284 0.133 Uiso 1 1 calc R .
loop_
_atom_type_symbol
_atom_type_description
_atom_type_scat_dispersion_real
_atom_type_scat_dispersion_imag
_atom_type_scat_source
C C 0.0033 0.0016 'International Tables Vol C Tables 4.2.6.8 and 6.1.1.4'
H H 0.0000 0.0000 'International Tables Vol C Tables 4.2.6.8 and 6.1.1.4'
N N 0.0061 0.0033 'International Tables Vol C Tables 4.2.6.8 and 6.1.1.4'
O O 0.0106 0.0060 'International Tables Vol C Tables 4.2.6.8 and 6.1.1.4'
loop_
_geom_angle_atom_site_label_1
_geom_angle_atom_site_label_2
_geom_angle_atom_site_label_3
_geom_angle
C7 O2 C8 113.4(18)
H1A N1 H1B 106.3
C1 N1 H1A 112.0
C1 N1 H1B 113.5
C3 C4 C5 120.0
C3 C4 C7 121.7(7)
C5 C4 C7 118.3(7)
C4 C3 H3 120.0
C4 C3 C2 120.0
C2 C3 H3 120.0
C3 C2 H2 120.0
C3 C2 C1 120.0
C1 C2 H2 120.0
N1 C1 C2 120.1(7)
N1 C1 C6 119.9(7)
C2 C1 C6 120.0
C1 C6 H6 120.0
C5 C6 C1 120.0
C5 C6 H6 120.0
C4 C5 H5 120.0
C6 C5 C4 120.0
C6 C5 H5 120.0
O1 C7 O2 122.9(19)
O1 C7 C4 127.3(12)
O2 C7 C4 109.8(16)
H9A C9 H9B 109.5
H9A C9 H9C 109.5
H9B C9 H9C 109.5
C8 C9 H9A 109.5
C8 C9 H9B 109.5
C8 C9 H9C 109.5
O2 C8 C9 107.1(17)
O2 C8 H8A 110.3
O2 C8 H8B 110.3
C9 C8 H8A 110.3
C9 C8 H8B 110.3
H8A C8 H8B 108.5
loop_
_geom_bond_atom_site_label_1
_geom_bond_atom_site_label_2
_geom_bond_distance
O1 C7 1.22(3)
O2 C7 1.346(14)
O2 C8 1.47(3)
N1 H1A 0.8792
N1 H1B 0.8807
N1 C1 1.330(19)
C4 C3 1.3900
C4 C5 1.3900
C4 C7 1.501(19)
C3 H3 0.9300
C3 C2 1.3900
C2 H2 0.9300
C2 C1 1.3900
C1 C6 1.3900
C6 H6 0.9300
C6 C5 1.3900
C5 H5 0.9300
C9 H9A 0.9600
C9 H9B 0.9600
C9 H9C 0.9600
C9 C8 1.524(12)
C8 H8A 0.9700
C8 H8B 0.9700
loop_
_cod_related_entry_id
_cod_related_entry_database
_cod_related_entry_code
1 PubChem 2337
