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CAS No.: 1393477-72-9
                                    
                                
 
                                 
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                            The BI-3802 was designed by Boehringer Ingelheim and could be obtained free of charge through the Boehringer Ingelheim open innovation portal opnMe.com, associated with its negative control.
KPT-330, analog of KPT-185, is an orally bioavailable selective CRM1 inhibitor.
Synonyms: KPT-330; ATG-010
 
                
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        					 *For Research Use Only !
        				
        				*For Research Use Only !
        			
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    							Batch number can be found on the product's label following the word 'Batch'.
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Search for reports by entering the product batch number.
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| CAS No. : | 1393477-72-9 | 
| Formula : | C17H11F6N7O | 
| M.W : | 443.31 | 
| SMILES Code : | O=C(NNC1=NC=CN=C1)/C=C\N2N=C(C3=CC(C(F)(F)F)=CC(C(F)(F)F)=C3)N=C2 | 
| Synonyms : | 
                                KPT-330; ATG-010
                             | 
| MDL No. : | MFCD27987944 | 
| InChI Key : | DEVSOMFAQLZNKR-RJRFIUFISA-N | 
| Pubchem ID : | 71481097 | 
| GHS Pictogram: |   | 
| Signal Word: | Warning | 
| Hazard Statements: | H302-H315-H319-H335 | 
| Precautionary Statements: | P261-P305+P351+P338 | 
| Target | 
 | 
In Vitro:
| Cell Line | Concentration | Treated Time | Description | References | 
| WiT49 | 100 nM | 48 hours | Evaluate the effect of selinexor on cell cycle and apoptosis, showing decreased nuclear XPO1 levels and a marginal increase in p21 | Med. 2022 Nov 11;3(11):774-791.e7. | 
| KPMRT-NS | 30 nM | 6 and 24 hours | Evaluate the effect of selinexor on XPO1 activity, showing a significant decrease in XPO1 activity at 6 and 24 hours | Med. 2022 Nov 11;3(11):774-791.e7. | 
| G401 | 30 nM | 6 and 24 hours | Evaluate the effect of selinexor on XPO1 activity, showing a significant decrease in XPO1 activity at 24 hours | Med. 2022 Nov 11;3(11):774-791.e7. | 
| OCI-AML2 | 200 nM | 48 h | To validate the activation of AKT signaling by Selinexor, results showed that Selinexor treatment significantly increased AKT phosphorylation. | Nat Cancer. 2022 Jul;3(7):837-851. | 
| MOLM-13 | 75 nM | 36 h | To validate the transcriptional upregulation of P2RY2 by Selinexor, results showed that Selinexor treatment significantly increased P2RY2 expression. | Nat Cancer. 2022 Jul;3(7):837-851. | 
| AML cells | 100 nM | 16 h | To assess the drug-induced increase in mitochondrial apoptotic priming using Dynamic BH3 profiling to predict tumor cell response to therapy. | Leukemia. 2016 Jan;30(1):190-9. | 
| WSU-FSCCL | 100 nM | 72 h | Selinexor combined with DEX or EVER significantly enhanced cytotoxicity in WSU-FSCCL cells | Cancer Lett. 2016 Dec 28;383(2):309-317. | 
| WSU-DLCL2 | 100 nM | 72 h | Selinexor combined with DEX or EVER significantly enhanced cytotoxicity in WSU-DLCL2 cells | Cancer Lett. 2016 Dec 28;383(2):309-317. | 
| Neuroblastoma cells | 23.4–365.8 nM | 72 h | To evaluate the cytotoxic effects of Selinexor on neuroblastoma cells, results showed that Selinexor induced cell death, and TP53 wild-type cells were more sensitive than mutant cells. | Neoplasia. 2022 Apr;26:100776. | 
| P493-6 B cells | 1μM | 6 h | To evaluate the effect of XPO1 inhibition on MYC-induced replication stress, results showed that XPO1 inhibition increased DNA damage and caused G2-M phase cell cycle arrest. | Cancer Res. 2024 Jan 2;84(1):101-117. | 
| OCI-Ly1 cells | 1μM | 24 h | To evaluate the effect of XPO1 inhibition on the expression of DNA damage repair proteins, results showed that XPO1 inhibition reduced the expression of CHEK1, RAD51, and WEE1. | Cancer Res. 2024 Jan 2;84(1):101-117. | 
| OCI-AML2 | 200 nM | 24 h | To validate selinexor’s ability to activate PI3K/AKT signaling, the results showed a significant increase in AKT phosphorylation after selinexor treatment. | Nat Cancer. 2022 Jul;3(7):837-851. | 
| MOLM-13 | 75 nM | 24 h | To validate selinexor’s ability to activate PI3K/AKT signaling, the results showed a significant increase in AKT phosphorylation after selinexor treatment. | Nat Cancer. 2022 Jul;3(7):837-851. | 
| MV4;11 | 50 nM | 24 h | To validate selinexor’s ability to activate PI3K/AKT signaling, the results showed a significant increase in AKT phosphorylation after selinexor treatment. | Nat Cancer. 2022 Jul;3(7):837-851. | 
| HL-60 | 300 nM | 24 h | To validate selinexor’s ability to activate PI3K/AKT signaling, the results showed a significant increase in AKT phosphorylation after selinexor treatment. | Nat Cancer. 2022 Jul;3(7):837-851. | 
| OCI-AML3 | 250 nM | 24 h | To validate selinexor’s ability to activate PI3K/AKT signaling, the results showed a significant increase in AKT phosphorylation after selinexor treatment. | Nat Cancer. 2022 Jul;3(7):837-851. | 
In Vivo:
| Species | Animal Model | Administration | Dosage | Frequency | Description | References | 
| SCID mice | MDA-MB-468 xenograft model | Oral | 5-25 mg/kg | Twice weekly or once weekly for 42 days | To evaluate the effect of KPT-330 on MDA-MB-468 xenograft model tumor growth, results showed that KPT-330 significantly inhibited tumor growth | Mol Cancer Ther. 2014 Mar;13(3):675-86. | 
| Mice | MLL-AF9-driven AML model | Oral | 15 mg/kg | Every other day for five cycles | To evaluate the efficacy of Selinexor combined with AKT inhibitor in AML mouse models, results showed that the combination therapy significantly prolonged survival. | Nat Cancer. 2022 Jul;3(7):837-851. | 
| NSG mice | Patient-derived AML xenograft model | Oral | 20 mg/kg | Three times a week for 4 weeks | To evaluate the antileukemic activity of Selinexor against AML cells, results showed that Selinexor significantly reduced the AML burden and was highly cytotoxic to leukemia-initiating cells (LICs). | Leukemia. 2016 Jan;30(1):190-9. | 
| Mice | WSU-DLCL2 subcutaneous tumor model | Oral | 10 mg/kg | Every other day for three weeks | Selinexor combined with DEX or EVER significantly inhibited tumor growth in the WSU-DLCL2 subcutaneous tumor model | Cancer Lett. 2016 Dec 28;383(2):309-317. | 
| Mice | A2780-res1 orthotopic ovarian cancer model | Orally | 20 mg/kg | Twice weekly, until mice became moribund | ERBB3 depletion restored the anti-tumor effect of selinexor | Mol Cancer Ther. 2020 Aug;19(8):1727-1735. | 
| Mice | Neuroblastoma xenograft models | Oral | 15 mg/kg | Twice weekly for 3 weeks | To evaluate the anti-tumor effects of Selinexor combined with Alisertib in neuroblastoma xenograft models, results showed that the combination therapy significantly inhibited tumor growth and induced tumor regression. | Neoplasia. 2022 Apr;26:100776. | 
| NSG mice | Patient-derived tumor xenograft (PDTX) model | Oral | 7.5 mg/kg | According to the dosing schedule shown in Fig. 3B | To evaluate the effect of XPO1 inhibition combined with CHOP on tumor growth, results showed that the combination significantly suppressed tumor growth and increased apoptosis. | Cancer Res. 2024 Jan 2;84(1):101-117. | 
| Mice | MLL-AF9-driven AML model | Oral | 15 mg/kg | Every other day for five weeks | To evaluate the efficacy of Selinexor combined with Ipatasertib in AML mouse models, the results showed that the combination significantly prolonged the survival of the mice. | Nat Cancer. 2022 Jul;3(7):837-851. | 
Clinical Trial:
| NCT Number | Conditions | Phases | Recruitment | Completion Date | Locations | 
| NCT02078349 | Solid Tumors | PHASE1 | COMPLETED | 2020-03-20 | National University Hospital, ... More >>Singapore, 119228, Singapore Less << | 
| NCT02250885 | Carcinoma, Neuroendocrine | PHASE2 | COMPLETED | 2025-08-16 | Gabrail Cancer Center Research... More >>, Canton, Ohio, 44718, United States Less << | 
| NCT03944057 | Relapse/Refractory Multiple My... More >>eloma Less << | PHASE2 | COMPLETED | 2022-02-25 | Beijing Chao-Yang Hospital, Ca... More >>pital Medical University, Beijing, Beijing, 100020, China|Peking University Third Hospital, Beijing, Beijing, 100191, China|Guangdong Provincial Peoples Hospital, Guangzhou, Guangdong, 510000, China|Nanfang Hospital, Guangzhou, Guangdong, 510515, China|Sun Yat-Sen University Cancer Center, Guanzhou, Guangdong, 510060, China|Henan Cancer Hospital, Zhengzhou, Henan, 450003, China|The Third Xiangya Hospital of Central Suoth University, Changsha, Hunan, 410013, China|The First Affilate Hospital with Nanjing Medical University, Nanjing, Jiangsu, 210029, China|The First Affiliated Hospital of Soochow University, Suzhou, Jiangsu, 215006, China|The First Affiliated Hospital of Nanchang University, Nanchang, Jiangxi, 330006, China|The First Bethune Hospital of Jilin University, Changchun, Jilin, 130021, China|Shengjing Hospital of China Medical University, Shenyang, Liaoning, 110004, China|Shanghai Changzheng Hospital, Shanghai, Shanghai, 200003, China|Shanghai Sixth People's Hospital Affiliate Shanghai JiaoTong University, Shanghai, Shanghai, 200233, China|Xijing Hospital, Xi'an, Shanxi, 710032, China|Tianjin blood research institute, Tianjin, Tianjin, 300020, China|The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang, 310003, China Less << | 
| NCT06552559 | B-cell Lymphoma Recurrent|B-ce... More >>ll Lymphoma Refractory|CNS Metastases Less << | PHASE1|PHASE2 | RECRUITING | 2027-12-30 | Samsung Cancer Research Instit... More >>ute, Seoul, 135-710, Korea, Republic of|Samsung Medical Center, Seoul, 135-710, Korea, Republic of Less << | 
| NCT01607892 | Hematological Malignancies | PHASE1 | COMPLETED | 2015-10-13 | Moffitt Cancer Center, Tampa, ... More >>Florida, 33612, United States|Dana-Farber Cancer Institute, Boston, Massachusetts, 02215, United States|Washington University School of Medicine, Saint Louis, Missouri, 63110, United States|Hackensack University Medical Center, Hackensack, New Jersey, 07601, United States|Weill Cornell Medical Center, New York, New York, 10065, United States|Gabrail Cancer Center Research, Canton, Ohio, 44718, United States|The Ohio State University, Columbus, Ohio, 43210, United States|Sarah Cannon Research Institute, Nashville, Tennessee, 37203, United States|MD Anderson Cancer Center, Houston, Texas, 77030, United States|Tom Baker Cancer Centre, Calgary, Alberta, T2W 4N2, Canada|Princess Margaret Hospital, Toronto, Ontario, M5T 2M9, Canada|Rigshospitalet, Copenhagen, 2100, Denmark Less << | 
| NCT02431351 | Myelodysplastic Syndrome | PHASE2 | WITHDRAWN | 2025-05-19 | - | 
| NCT03627403 | Primary Myelofibrosis|Post-ess... More >>ential Thrombocythemia Myelofibrosis|Post-polycythemia Vera Myelofibrosis Less << | PHASE2 | ACTIVE_NOT_RECRUITING | 2025-03-14 | Huntsman Cancer Institute/Univ... More >>ersity of Utah, Salt Lake City, Utah, 84112, United States Less << | 
| NCT02091245 | Relapsed Acute Lymphoblastic L... More >>eukemia (ALL)|Refractory Acute Lymphoblastic Leukemia (ALL)|Relapsed Acute Myelogenous Leukemia (AML)|Refractory Acute Myelogenous Leukemia (AML)|Relapsed Mixed Lineage Leukemia|Refractory Mixed Lineage Leukemia|Relapsed Biphenotypic Leukemia|Refractory Biphenotypic Leukemia|Chronic Myelogenous Leukemia (CML) in Blast Crisis Less << | PHASE1 | ACTIVE_NOT_RECRUITING | 2025-06-25 | UCSF, San Francisco, Californi... More >>a, 94143, United States|Children's Hospital Colorado, Aurora, Colorado, 80045, United States|Children's Healthcare of Atlanta, Atlanta, Georgia, 30322, United States|Boston Children's Hospital, Boston, Massachusetts, 02115, United States|Dana-Farber Cancer Institute, Boston, Massachusetts, 02215, United States|Columbia University Medical Center, New York, New York, 10032, United States|Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, 19104, United States|Texas Children's Hospital, Houston, Texas, 77030, United States|Seattle Children's Hospital, Seattle, Washington, 98101, United States|Children's Hospital of Wisconsin, Milwaukee, Wisconsin, 53226, United States Less << | 
| NCT05852028 | Lymphoma|DLBCL|T Cell Lymphoma | RECRUITING | 2025-10-18 | Ruijin Hospital, Shanghai Jiao... More >> Tong University School of Medicine, Shanghai, Shanghai, 200025, China|The First Affiliated Hospital of Soochow University, Suzhou, China|Union Hospital Affiliated to Huazhong University of Science and Technology, Wuhan, China Less << | |
| NCT03466827 | Thymoma|Advanced Thymic Epithe... More >>lial Tumour Less << | PHASE2 | UNKNOWN | 2020-07-01 | Rigshospitalet, Copenhagen, 21... More >>00, Denmark|Hospices Civils de Lyon, Lyon, France|Intitut Curie, Paris, France|Intitut Gustave Roussy, Paris, France Less << | 
| NCT04355676 | Coronavirus Infection | PHASE2 | WITHDRAWN | 2020-08-30 | - | 
| NCT02146833 | Prostate Cancer | PHASE2 | TERMINATED | 2016-04-01 | M.D. Anderson Cancer Center, H... More >>ouston, Texas, 77030, United States Less << | 
| NCT05954780 | Multiple Myeloma | RECRUITING | 2026-09-15 | Medizinische Universit?t Wien,... More >> Universit?tsklinik für Innere Medizin I, Wien, 1090, Austria|Gemeinschaftspraxis für H?matologie und Onkologie GbR, Ravensburg, Baden-Württemberg, 88212, Germany Less << | |
| NCT05822050 | PTCL Patients Who Achieved Com... More >>plete Response From Frontline Treatment Less << | PHASE2|PHASE3 | RECRUITING | 2025-06-30 | The First Bethune Hospital of ... More >>Jilin University, Changchun, Jilin, 130021, China Less << | 
| NCT03850704 | Multiple Myeloma | NO_LONGER_AVAILABLE | - | - | |
| NCT02402764 | Breast Cancer | PHASE2 | COMPLETED | 2019-06-06 | H. Lee Moffitt Cancer Center a... More >>nd Research Institute, Tampa, Florida, 33612, United States Less << | 
| NCT06452446 | Multiple Myeloma|Large-cell Ly... More >>mphoma Less << | NOT_YET_RECRUITING | 2028-07-01 | - | |
| NCT02215161 | Castration Levels of Testoster... More >>one|Hormone-Resistant Prostate Cancer|Metastatic Prostate Carcinoma in the Soft Tissue|Prostate Carcinoma Metastatic in the Bone|PSA Progression|Stage IV Prostate Adenocarcinoma AJCC v7 Less << | PHASE2 | TERMINATED | 2018-04-02 | University of California, San ... More >>Francisco, San Francisco, California, 94115, United States Less << | 
| NCT05597345 | Smoldering Multiple Myeloma | PHASE2 | RECRUITING | 2024-12-31 | University of Rochester, Roche... More >>ster, New York, 14642, United States Less << | 
| NCT01986348 | Glioblastoma|Glioma | PHASE2 | TERMINATED | 2020-01-23 | Massachusetts General Hospital... More >>, Boston, Massachusetts, 02114, United States|Dana Farber Cancer Institute, Center for Neuro-Oncology, Boston, Massachusetts, 02215, United States|Columbia University, Herbert Irving Comprehensive Cancer Center, New York, New York, 10032, United States|The Phase I Unit, Dept. of Oncology, Rigshospitalet, Copenhagen, DK-2100, Denmark|University of Groningen Faculty of Medical Sciences, Medical Oncology, Groningen, 9713 GZ, Netherlands|Erasmus MC-Daniel den Hoed Cancer Center- Neuro-Oncology Unit, Rotterdam, 3008AE, Netherlands Less << | 
| NCT03147885 | Diffuse Large B-Cell Lymphoma|... More >>Recurrent B-Cell Non-Hodgkin Lymphoma|Recurrent Extranodal Marginal Zone Lymphoma|Recurrent Follicular Lymphoma|Recurrent Indolent Adult Non-Hodgkin Lymphoma|Recurrent Mantle Cell Lymphoma|Recurrent Marginal Zone Lymphoma|Recurrent Waldenstrom Macroglobulinemia|Refractory B-Cell Non-Hodgkin Lymphoma|Refractory Extranodal Marginal Zone Lymphoma|Refractory Follicular Lymphoma|Refractory Mantle Cell Lymphoma|Stage III Non-Hodgkin Lymphoma|Stage IV Non-Hodgkin Lymphoma|Transformed Recurrent Non-Hodgkin Lymphoma Less << | PHASE1|PHASE2 | RECRUITING | 2025-12-26 | Barbara Ann Karmanos Cancer In... More >>stitute, Detroit, Michigan, 48201, United States Less << | 
| NCT05985161 | Wilms Tumor|Rhabdoid Tumor|Mal... More >>ignant Peripheral Nerve Sheath Tumors|MPNST|Nephroblastoma|XPO1 Gene Mutation|Solid Tumor Less << | PHASE2 | RECRUITING | 2029-08-01 | Children's Hospital of Los Ang... More >>eles (Data Collection Only), Los Angeles, California, 90027, United States|Children's Healthcare of Atlanta (Data Collection and Specimen Analysis), Atlanta, Georgia, 30322, United States|Dana Farber Cancer Institute (Data Collection Only), Boston, Massachusetts, 02115, United States|Memorial Sloan Kettering at Basking Ridge (Limited Protocol Activities), Basking Ridge, New Jersey, 07920, United States|Memorial Sloan Kettering Monmouth (Limited Protocol Activities), Middletown, New Jersey, 07748, United States|Memorial Sloan Kettering Bergen (Limited protocol activities), Montvale, New Jersey, 07645, United States|Memorial Sloan Kettering Suffolk-Commack (Limited Protocol Activities ), Commack, New York, 11725, United States|Memorial Sloan Kettering Westchester (Limited Protocol Activities), Harrison, New York, 10604, United States|Memorial Sloan Kettering Cancer Center (All protocol activites), New York, New York, 10065, United States|Memorial Sloan Kettering Nassau (Limited protocol activities), Rockville Centre, New York, 11553, United States|Cincinnati Children's Hospital Medical Center (Data collection only), Cincinnati, Ohio, 45229, United States Less << | 
| NCT02025985 | Ovarian Carcinoma|Endometrial ... More >>Carcinoma|Cervical Carcinoma Less << | PHASE2 | COMPLETED | 2017-03-29 | UZ Leuven - Universitair Zieke... More >>nhuis Leuven, Leuven, B-3000, Belgium|Aalborg University Hospital, Aalborg, DK-9100, Denmark|Rigshospitalet, Copenhagen, DK-2100, Denmark|Herlev Hospital, Herlev, DK-2730, Denmark Less << | 
| NCT04595994 | Sarcoma,Soft Tissue | PHASE1 | RECRUITING | 2026-05-31 | Hospital de la Santa Creu i Sa... More >>nt Pau, Barcelona, 08025, Spain|HU Vall d'Hebron, Barcelona, 08035, Spain|H. Fundación Jiménez Díaz, Madrid, 28040, Spain|Hospital Clínico San Carlos, Madrid, 28040, Spain|Hospital Universitario La Paz, Madrid, 28046, Spain|Hospital Universitario Miguel Servet, Zaragoza, 50009, Spain Less << | 
| NCT04811196 | Soft Tissue Sarcoma|Malignant ... More >>Peripheral Nerve Sheath Tumor (MPNST)|Leiomyosarcoma|Endometrial Stromal Sarcoma Less << | PHASE1 | ACTIVE_NOT_RECRUITING | 2025-02-25 | Princess Margaret Cancer Centr... More >>e, Toronto, Ontario, M5G 2M9, Canada Less << | 
| NCT02314247 | Peripheral T-cell Lymphoma (PT... More >>CL)|Cutaneous T-cell Lymphoma (CTCL) Less << | PHASE2 | TERMINATED | 2025-02-16 | Concord Repatriation General H... More >>ospital (CRGH), Concord, New South Wales, 2139, Australia|Royal North Shore Hospital, St. Leonards, New South Wales, 2139, Australia|Westmead Hospital, Westmead, New South Wales, 2145, Australia|Cabrini Hospital, Malvern, Victoria, Australia|National Cancer Centre, Singapore, 169610, Singapore Less << | 
| Bio Calculators | ||||
| Preparing Stock Solutions |  | 1mg | 5mg | 10mg | 
| 1 mM 5 mM 10 mM | 2.26mL 0.45mL 0.23mL | 11.28mL 2.26mL 1.13mL | 22.56mL 4.51mL 2.26mL | |
Tags: Selinexor | KPT-330 | KPT330 | KPT 330 | Xpovio | selective inhibitor of nuclear export | exportin 1 | SINE | XPO1 | apoptosis | apoptosis | XPO1 inhibitor | multiple myeloma | DLBCL | p53 | 1393477-72-9
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| P390 | Absorb spillage to prevent material damage. | 
| P391 | Collect spillage. Hazardous to the aquatic environment | 
| P301 + P310 | IF SWALLOWED: Immediately call a POISON CENTER or doctor/physician. | 
| P301 + P312 | IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell. | 
| P301 + P330 + P331 | IF SWALLOWED: Rinse mouth. Do NOT induce vomiting. | 
| P302 + P334 | IF ON SKIN: Immerse in cool water/wrap in wet bandages. | 
| P302 + P350 | IF ON SKIN: Gently wash with plenty of soap and water. | 
| P303 + P361 + P353 | IF ON SKIN (or hair): Remove/Take off Immediately all contaminated clothing. Rinse SKIN with water/shower. | 
| P304 + P312 | IF INHALED: Call a POISON CENTER or doctor/physician if you feel unwell. | 
| P304 + P340 | IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing. | 
| P304 + P341 | IF INHALED: If breathing is difficult, remove victim to fresh air and keep at rest in a position comfortable for breathing. | 
| P305 + P351 + P338 | IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. | 
| P306 + P360 | IF ON CLOTHING: Rinse Immediately contaminated CLOTHING and SKIN with plenty of water before removing clothes. | 
| P307 + P311 | IF exposed: call a POISON CENTER or doctor/physician. | 
| P308 + P313 | IF exposed or concerned: Get medical advice/attention. | 
| P309 + P311 | IF exposed or if you feel unwell: call a POISON CENTER or doctor/physician. | 
| P332 + P313 | IF SKIN irritation occurs: Get medical advice/attention. | 
| P333 + P313 | IF SKIN irritation or rash occurs: Get medical advice/attention. | 
| P335 + P334 | Brush off loose particles from skin. Immerse in cool water/wrap in wet bandages. | 
| P337 + P313 | IF eye irritation persists: Get medical advice/attention. | 
| P342 + P311 | IF experiencing respiratory symptoms: call a POISON CENTER or doctor/physician. | 
| P370 + P376 | In case of fire: Stop leak if safe to Do so. | 
| P370 + P378 | In case of fire: | 
| P370 + P380 | In case of fire: Evacuate area. | 
| P370 + P380 + P375 | In case of fire: Evacuate area. Fight fire remotely due to the risk of explosion. | 
| P371 + P380 + P375 | In case of major fire and large quantities: Evacuate area. Fight fire remotely due to the risk of explosion. | 
| Storage | |
| Code | Phrase | 
| P401 | |
| P402 | Store in a dry place. | 
| P403 | Store in a well-ventilated place. | 
| P404 | Store in a closed container. | 
| P405 | Store locked up. | 
| P406 | Store in corrosive resistant/ container with a resistant inner liner. | 
| P407 | Maintain air gap between stacks/pallets. | 
| P410 | Protect from sunlight. | 
| P411 | |
| P412 | Do not expose to temperatures exceeding 50 oC/ 122 oF. | 
| P413 | |
| P420 | Store away from other materials. | 
| P422 | |
| P402 + P404 | Store in a dry place. Store in a closed container. | 
| P403 + P233 | Store in a well-ventilated place. Keep container tightly closed. | 
| P403 + P235 | Store in a well-ventilated place. Keep cool. | 
| P410 + P403 | Protect from sunlight. Store in a well-ventilated place. | 
| P410 + P412 | Protect from sunlight. Do not expose to temperatures exceeding 50 oC/122oF. | 
| P411 + P235 | Keep cool. | 
| Disposal | |
| Code | Phrase | 
| P501 | Dispose of contents/container to ... | 
| P502 | Refer to manufacturer/supplier for information on recovery/recycling | 
| Physical hazards | |
| Code | Phrase | 
| H200 | Unstable explosive | 
| H201 | Explosive; mass explosion hazard | 
| H202 | Explosive; severe projection hazard | 
| H203 | Explosive; fire, blast or projection hazard | 
| H204 | Fire or projection hazard | 
| H205 | May mass explode in fire | 
| H220 | Extremely flammable gas | 
| H221 | Flammable gas | 
| H222 | Extremely flammable aerosol | 
| H223 | Flammable aerosol | 
| H224 | Extremely flammable liquid and vapour | 
| H225 | Highly flammable liquid and vapour | 
| H226 | Flammable liquid and vapour | 
| H227 | Combustible liquid | 
| H228 | Flammable solid | 
| H229 | Pressurized container: may burst if heated | 
| H230 | May react explosively even in the absence of air | 
| H231 | May react explosively even in the absence of air at elevated pressure and/or temperature | 
| H240 | Heating may cause an explosion | 
| H241 | Heating may cause a fire or explosion | 
| H242 | Heating may cause a fire | 
| H250 | Catches fire spontaneously if exposed to air | 
| H251 | Self-heating; may catch fire | 
| H252 | Self-heating in large quantities; may catch fire | 
| H260 | In contact with water releases flammable gases which may ignite spontaneously | 
| H261 | In contact with water releases flammable gas | 
| H270 | May cause or intensify fire; oxidizer | 
| H271 | May cause fire or explosion; strong oxidizer | 
| H272 | May intensify fire; oxidizer | 
| H280 | Contains gas under pressure; may explode if heated | 
| H281 | Contains refrigerated gas; may cause cryogenic burns or injury | 
| H290 | May be corrosive to metals | 
| Health hazards | |
| Code | Phrase | 
| H300 | Fatal if swallowed | 
| H301 | Toxic if swallowed | 
| H302 | Harmful if swallowed | 
| H303 | May be harmful if swallowed | 
| H304 | May be fatal if swallowed and enters airways | 
| H305 | May be harmful if swallowed and enters airways | 
| H310 | Fatal in contact with skin | 
| H311 | Toxic in contact with skin | 
| H312 | Harmful in contact with skin | 
| H313 | May be harmful in contact with skin | 
| H314 | Causes severe skin burns and eye damage | 
| H315 | Causes skin irritation | 
| H316 | Causes mild skin irritation | 
| H317 | May cause an allergic skin reaction | 
| H318 | Causes serious eye damage | 
| H319 | Causes serious eye irritation | 
| H320 | Causes eye irritation | 
| H330 | Fatal if inhaled | 
| H331 | Toxic if inhaled | 
| H332 | Harmful if inhaled | 
| H333 | May be harmful if inhaled | 
| H334 | May cause allergy or asthma symptoms or breathing difficulties if inhaled | 
| H335 | May cause respiratory irritation | 
| H336 | May cause drowsiness or dizziness | 
| H340 | May cause genetic defects | 
| H341 | Suspected of causing genetic defects | 
| H350 | May cause cancer | 
| H351 | Suspected of causing cancer | 
| H360 | May damage fertility or the unborn child | 
| H361 | Suspected of damaging fertility or the unborn child | 
| H361d | Suspected of damaging the unborn child | 
| H362 | May cause harm to breast-fed children | 
| H370 | Causes damage to organs | 
| H371 | May cause damage to organs | 
| H372 | Causes damage to organs through prolonged or repeated exposure | 
| H373 | May cause damage to organs through prolonged or repeated exposure | 
| Environmental hazards | |
| Code | Phrase | 
| H400 | Very toxic to aquatic life | 
| H401 | Toxic to aquatic life | 
| H402 | Harmful to aquatic life | 
| H410 | Very toxic to aquatic life with long-lasting effects | 
| H411 | Toxic to aquatic life with long-lasting effects | 
| H412 | Harmful to aquatic life with long-lasting effects | 
| H413 | May cause long-lasting harmful effects to aquatic life | 
| H420 | Harms public health and the environment by destroying ozone in the upper atmosphere | 
Sorry,this product has been discontinued.
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