1-Aminobenzotriazole - 10mM in DMSO , CAS No.1614-12-6

CAS: 1614-12-6 Cat. No.: A421948 Peso molecular: 134.14 Beilstein Registry Number: 607843 Número EC: 633-910-7
Disponible para pedir
GRADE & PURITY 10mM in DMSO
Synonyms
Lopac0_000056 | AKOS001013369 | Q-102063 | HY-103389 | 1H-benzo[d][1,2,3]triazol-1-amine | LP00056 | NCGC00015056-01 | SMR000326746 | MFCD00132902 | 1-Benzotriazolamine | BDBM50106744 | EU-0100056 | NCGC00015056-02 | HMS2235A14 | Tox21_500056 | SR-0100007
Storage
Store at -80°C
Shipped In
Dry ice packs + Cold packs
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
1ml
A421948-1ml
1

58,90US$

69,90US$
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Why this grade

10mM in DMSO for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Store at -80°C Ships Dry ice packs + Cold packs Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 16 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

1-Aminobenzotriazole (ABT) is a non-specific cytochrome P450 (CYP) inhibitor.

Specifications

Sinónimos
Lopac0_000056 | AKOS001013369 | Q-102063 | HY-103389 | 1H-benzo[d][1, 2, 3]triazol-1-amine | LP00056 | NCGC00015056-01 | SMR000326746 | MFCD00132902 | 1-Benzotriazolamine | BDBM50106744 | EU-0100056 | NCGC00015056-02 | HMS2235A14 | Tox21_500056 | SR-0100007
Especificaciones y pureza
10mM in DMSO
Mecanismos bioquímicos y fisiológicos
Cytochrome P450 inhibitor. Inhibits synthesis of the eicosanoid 20-hydroxyeicosatetraenoic acid (20-HETE). Reduces intimal hyperplasia and vascular remodeling following endothelial injury in rat carotid arteries.
Condiciones de almacenamiento de almacenamiento
Store at -80°C
Enviado en
Dry ice packs + Cold packs
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Tipo de acción
INHIBITOR
Nombres e identificadores
Sonrisas canónicasC1=CC=C2C(=C1)N=NN2N
IUPAC Namebenzotriazol-1-amine
InChIKeyJCXKHYLLVKZPKE-UHFFFAOYSA-N
INCHI1S/C6H6N4/c7-10-6-4-2-1-3-5(6)8-9-10/h1-4H,7H2
Isómeros SMILES C1=CC=C2C(=C1)N=NN2N
WGK Alemania 3
RTECS DM1235000
Peso molecular 134.14
Beilstein 607843
Reaxy-Rn 607843
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=607843&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
ClaseBenzotriazoles
SubclassNot available
Intermediate Tree Nodes Not available
Direct ParentBenzotriazoles
Alternative Parents Benzenoids  Triazoles  Heteroaromatic compounds  Azacyclic compounds  Organopnictogen compounds  Organonitrogen compounds  Hydrocarbon derivatives  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Benzotriazole - Benzenoid - Heteroaromatic compound - 1,2,3-triazole - Triazole - Azole - Azacycle - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Aromatic heteropolycyclic compound
DescripciónThis compound belongs to the class of organic compounds known as benzotriazoles. These are organic compounds containing a benzene fused to a triazole ring (a five-membered ring with two carbon atoms and three nitrogen atoms).
External Descriptors Not available
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
CYP3A4 Tclin Cytochrome P450 3A4 (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
PDE5A Tclin Phosphodiesterase 5A (5113 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
EGFR Tclin Epidermal growth factor receptor erbB1 (33727 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA2 Tclin Carbonic anhydrase II (17698 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ESR1 Tclin Estrogen receptor alpha (17718 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HMGCR Tclin HMG-CoA reductase (2475 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NR3C1 Tclin Glucocorticoid receptor (14987 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
INSR Tclin Insulin receptor (5558 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PGR Tclin Progesterone receptor (8562 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADRB2 Tclin Beta-2 adrenergic receptor (11824 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CHRM2 Tclin Muscarinic acetylcholine receptor M2 (10671 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADRB1 Tclin Beta-1 adrenergic receptor (6630 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HTR1A Tclin Serotonin 1a (5-HT1a) receptor (14969 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADRA2A Tclin Alpha-2a adrenergic receptor (9450 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
AR Tclin Androgen Receptor (11781 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CHRM1 Tclin Muscarinic acetylcholine receptor M1 (12690 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ACE Tclin Angiotensin-converting enzyme (1423 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
DRD2 Tclin Dopamine D2 receptor (23596 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MAOA Tclin Monoamine oxidase A (11911 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CNR1 Tclin Cannabinoid CB1 receptor (20913 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
DRD1 Tclin Dopamine D1 receptor (9720 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
DRD4 Tchem Dopamine D4 receptor (7907 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ACHE Tclin Acetylcholinesterase (18204 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PTGS1 Tclin Cyclooxygenase-1 (9233 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC6A2 Tclin Norepinephrine transporter (10102 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HRH2 Tclin Histamine H2 receptor (5428 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADRA1D Tclin Alpha-1d adrenergic receptor (4171 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HTR1B Tclin Serotonin 1b (5-HT1b) receptor (2801 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HTR2A Tclin Serotonin 2a (5-HT2a) receptor (14758 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HTR2C Tclin Serotonin 2c (5-HT2c) receptor (11471 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADORA1 Tclin Adenosine A1 receptor (17603 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CALCR Tclin Calcitonin receptor (2215 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC6A4 Tclin Serotonin transporter (12625 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADRA1A Tclin Alpha-1a adrenergic receptor (8359 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PTGS2 Tclin Cyclooxygenase-2 (13999 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HRH1 Tclin Histamine H1 receptor (7573 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADRA1B Tclin Alpha-1b adrenergic receptor (2912 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
OPRM1 Tclin Mu opioid receptor (19785 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
DRD3 Tclin Dopamine D3 receptor (14368 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
AVPR1A Tclin Vasopressin V1a receptor (5412 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
OPRD1 Tclin Delta opioid receptor (15096 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
OPRK1 Tclin Kappa opioid receptor (16155 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC6A3 Tclin Dopamine transporter (10535 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
KCNH2 Tclin HERG (29587 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HTR4 Tclin Serotonin 4 (5-HT4) receptor (2068 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ESR2 Tclin Estrogen receptor beta (9272 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYSLTR1 Tclin Cysteinyl leukotriene receptor 1 (2118 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ERBB2 Tclin Receptor protein-tyrosine kinase erbB-2 (7851 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CHRM4 Tclin Muscarinic acetylcholine receptor M4 (6041 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CHRM5 Tclin Muscarinic acetylcholine receptor M5 (4677 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADRA2B Tclin Alpha-2b adrenergic receptor (4412 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Objetivos asociados (no humanos)
Agtr2 Angiotensin II type 2 (AT-2) receptor (803 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mc4r Melanocortin receptor 4 (1205 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Ltc4s Leukotriene C4 synthase (1 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Sigmar1 Sigma opioid receptor (160 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Npy1r Neuropeptide Y receptor type 1 (8 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Cckar Cholecystokinin A receptor (90 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Nos2 Nitric oxide synthase, inducible (3573 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mapk1 MAP kinase ERK2 (650 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mmp9 Matrix metalloproteinase 9 (38 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Plasmodium falciparum (966862 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Hepatitis B virus (7925 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mapt Microtubule-associated protein tau (6 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Glra2 Glycine receptor (1745 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SARS-CoV-2 (38078 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Propiedades químicas y físicas
SensibilidadLight Sensitive,Moisture Sensitive
Punto de fusión (°C)84 °C
Peso molecular134.140 g/mol
XLogP30.900
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count3
Rotatable Bond Count0
Exact Mass134.059 Da
Monoisotopic Mass134.059 Da
Topological Polar Surface Area56.700 Ų
Heavy Atom Count10
Formal Charge0
Complexity127.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Citations of This Product
Referencias
1. Xin Wang, Guangyun Ran, Yufen Liao, Bowen Gong, Chutian Wu, Rong Tan, Ying Liu, Shiyu Zhang, Ying Peng, Weiwei Li, Jiang Zheng.  (2023)  Formation of RNA adducts resulting from metabolic activation of spice ingredient safrole mediated by P450 enzymes and sulfotransferases.  FOOD AND CHEMICAL TOXICOLOGY,      [PMID:36841326] [10.1016/j.fct.2023.113688]
2. Mingyu Zhang, Yaodong Hu, Wei Li, Chen Sun, Chunjing Guan, Ying Peng, Jiang Zheng.  (2022)  In Vitro and In Vivo Metabolic Activation and Hepatotoxicity of Environmental Pollutant 2,6-Dimethylphenol.  CHEMICAL RESEARCH IN TOXICOLOGY,      [PMID:35583464] [10.1021/acs.chemrestox.2c00048]
3. Fei Li, Lin Di, Yuxin Liu, Qiuyun Xiao, Xiaoyu Zhang, Fuying Ma, Hongbo Yu.  (2018)  Carbaryl biodegradation by Xylaria sp. BNL1 and its metabolic pathway.  ECOTOXICOLOGY AND ENVIRONMENTAL SAFETY,      [PMID:30359899] [10.1016/j.ecoenv.2018.10.051]
4. Yukang Wang, Gaochen Jin, Shuyan Song, Yijun Jin, Xiaowen Wang, Shuaiqi Yang, Xingxing Shen, Yinbo Gan, Yuexing Wang, Ran Li, Jian-Xiang Liu, Jianping Hu, Ronghui Pan.  (2024)  A peroxisomal cinnamate:CoA ligase-dependent phytohormone metabolic cascade in submerged rice germination.  DEVELOPMENTAL CELL,      [PMID:38579719] [10.1016/j.devcel.2024.03.023]
5. Sun Chen, Zhang Mingyu, Guan Chunjing, Li Weiwei, Peng Ying, Zheng Jiang.  (2024)  In vitro and in vivo metabolic activation and hepatotoxicity of chlorzoxazone mediated by CYP3A.  ARCHIVES OF TOXICOLOGY,      [PMID:38369618] [10.1007/s00204-023-03674-2]
6. Yuqian Chi, Xiaoliang Zhu, Yaxuan Chen, Xin Li, Ziyi Jiang, Xiaoyang Jian, Mengyuan Lian, Xiaodi Wu, Lei Wang, Mengmeng Sun, Xiaowei Shi.  (2024)  Metabolic activation and cytochrome P450 inhibition of piperlonguminine mediated by CYP3A4.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,      [PMID:38626834] [10.1016/j.ijbiomac.2024.131502]
7. Siyu Liu, Guode Zhao, Yingyun Xu, Yang Wang, Zifang Ding, Weiwei Li, Ying Peng, Jiang Zheng.  (2025)  Metabolic activation and hepatic cytotoxicity of osthole mediated by cytochrome P450 enzymes.  TOXICOLOGY LETTERS,      [PMID:39793773] [10.1016/j.toxlet.2024.12.009]
8. Li Shao, Jiajia Mo, Qinlong Xu, Guangwei He, Chunyu Xing, Zhaoxing Chu.  (2024)  Preclinical pharmacokinetic investigation of the bioavailability and skin distribution of HY-072808 ointment, a novel drug candidate for the treatment of atopic dermatitis, in minipigs by a newly LC-MS/MS method.  XENOBIOTICA,      [PMID:38501457] [10.1080/00498254.2024.2333007]
9. Yan He, Zihao Cheng, Jingyu Zhang, Yu Chen, Guode Zhao, Hong Tang, Yufen Liao, Tingmin Ye, Ying Peng, Weiwei Li, Jiang Zheng.  (2024)  RNA Adduction Resulting from the Metabolic Activation of Myristicin by P450 Enzymes and Sulfotransferases.  JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY,      [PMID:38959404] [10.1021/acs.jafc.4c01676]
10. Tingmin Ye, Chunping Tang, Dandan Yang, Qing Zhang, Yufen Liao, Jie Dai, Hong Tang, Changqiang Ke, Ying Peng, Yang Ye, Weiwei Li, Jiang Zheng.  (2025)  Metabolic activation and cytotoxicity of bavachin mediated by CYP3A in mice.  CHEMICO-BIOLOGICAL INTERACTIONS,      [PMID:40609922] [10.1016/j.cbi.2025.111630]
11. Aolin Ma, Siqi Liu, Zhixuan Du, Longfei Zhu, Guanping Feng.  (2025)  Sulfonamides impede duckweed growth by inducing an excessive accumulation of salicylic acid.  ENVIRONMENTAL AND EXPERIMENTAL BOTANY,      [PMID:] [10.1016/j.envexpbot.2025.106224]
12. Wei Wang, Jing Zhang, Gefei Huang, Iweta Pryjomska-Ray, Dietrich A. Volmer, Zongwei Cai.  (2025)  Tire-additive chemicals and their derivatives in urban road dust: Spatial distributions, exposures, and associations with tire and road wear particles.  JOURNAL OF HAZARDOUS MATERIALS,      [PMID:40024120] [10.1016/j.jhazmat.2025.137749]
13. Pinzheng Li, Hengbin Zhang, Yingchun Chen, Shuanghui Lu, Huidi Jiang, Su Zeng, Hui Zhou.  (2025)  CYP-mediated metabolic divergence underpins oxoglaucine selectivity: Detoxification in healthy hepatocytes versus mitochondrial apoptosis in hepatocellular carcinoma.  TOXICOLOGY IN VITRO,      [PMID:41173113] [10.1016/j.tiv.2025.106170]
14. Yuqin Chen, Zixia Hu, Guode Zhao, Mei Li, Ziying Jiang, Liangjia Xu, Jiannan Zheng, Weiwei Li, Ying Peng, Jiang Zheng.  (2025)  Metabolic activation, hepatic protein covalent binding, and cytotoxicity of arctigenin.  TOXICOLOGY LETTERS,      [PMID:41325899] [10.1016/j.toxlet.2025.111785]
15. Xiu Chen, Xiaoyi Pan, Jieping Zhao, Huihui Jin, Hengbin Zhang, Yongbiao Song, Hui Zhou, Jianbiao Yao, Huidi Jiang.  (2025)  Interactions of neocryptotanshinone and human cytochrome P450 in silico and in vitro.  TOXICOLOGY IN VITRO,      [PMID:41419033] [10.1016/j.tiv.2025.106191]
16. Lili Wu, Siyu Chen, Qiyuan Yang, Xing Li, Lingyan Liu, Shengjun Ji, Shuaiyuan Tang, Sihui Zhang, Yan Wang, Runzhi Chen, Zhikun Zhan.  (2026)  Cytochrome P450-Mediated Detoxification and NF-κB/NLRP3 Pathway-Driven Hepatotoxicity of Emodin: Multiomics and laboratory evidence.  CHEMICO-BIOLOGICAL INTERACTIONS,      [PMID:41579920] [10.1016/j.cbi.2026.111934]
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