4-Chloro-o-phenylenediamine - 97%, high purity , CAS No.95-83-0

2 Citations
  • ≥97%
Item Number
C122655
Grouped product items
SKUSizeAvailabilityPrice Qty
C122655-5g
5g
In stock
$15.90
C122655-10g
10g
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$27.90
C122655-25g
25g
In stock
$42.90
C122655-100g
100g
In stock
$153.90
C122655-500g
500g
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$692.90

Basic Description

Synonyms95-83-0 | 4-chlorobenzene-1,2-diamine | 4-Chloro-o-phenylenediamine | 4-Chloro-1,2-diaminobenzene | 4-Chloro-1,2-phenylenediamine | 1,2-Diamino-4-chlorobenzene | 1,2-Benzenediamine, 4-chloro- | Ursol Olive 6G | 3,4-Diaminochlorobenzene | 4-CHLORO-1,2-BENZENEDIAMINE | 2-Amino
Specifications & Purity≥97%
Storage TempArgon charged
Shipped InNormal
Product Description

Undergoes cyclizations and cyclocondensations to form benzimidazoles.

Associated Targets(Human)

CYP3A4 Tclin Cytochrome P450 3A4 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
ESR1 Tclin Estrogen receptor (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
NR3C1 Tclin Glucocorticoid receptor (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
RUNX1 Tbio Runt-related transcription factor 1 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
RORC Tchem Nuclear receptor ROR-gamma (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
SMN1 Tchem Survival motor neuron protein (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
RXRA Tclin Retinoic acid receptor RXR-alpha (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
TSHR Tclin Thyrotropin receptor (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
ALOX15 Tchem Arachidonate 15-lipoxygenase (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
NR1H4 Tclin Bile acid receptor (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
NR1I2 Tchem Nuclear receptor subfamily 1 group I member 2 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
AHR Tclin Aryl hydrocarbon receptor (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
AR Tclin Androgen receptor (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
ALDH1A1 Tchem Retinal dehydrogenase 1 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
THRB Tclin Thyroid hormone receptor beta (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
KCNH2 Tclin Potassium voltage-gated channel subfamily H member 2 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
PPARG Tclin Peroxisome proliferator-activated receptor gamma (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
NFE2L2 Tchem Nuclear factor erythroid 2-related factor 2 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
ESR1 Tclin Estrogen receptor alpha (17718 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NR3C1 Tclin Glucocorticoid receptor (14987 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
AR Tclin Androgen Receptor (11781 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TSHR Tclin Thyroid stimulating hormone receptor (29986 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PPARG Tclin Peroxisome proliferator-activated receptor gamma (15191 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
KCNH2 Tclin HERG (29587 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
THRB Tclin Thyroid hormone receptor beta-1 (7926 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
RXRA Tclin Retinoid X receptor alpha (3637 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
AHR Tclin Aryl hydrocarbon receptor (1071 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ALDH1A1 Tchem Aldehyde dehydrogenase 1A1 (77053 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NR1H4 Tclin Bile acid receptor FXR (6228 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ALOX15 Tchem Arachidonate 15-lipoxygenase (7108 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP3A4 Tclin Cytochrome P450 3A4 (53859 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Lymphoblastoid cell (5959 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SMN1 Tchem Survival motor neuron protein (34246 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
RUNX1 Tbio Runt-related transcription factor 1/Core-binding factor subunit beta (7867 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Mus musculus (284745 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Luciferin 4-monooxygenase (66902 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Nfe2l2 Nuclear factor erythroid 2-related factor 2 (214 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Rorc Nuclear receptor ROR-gamma (89407 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Nr1i2 Nuclear receptor subfamily 1 group I member 2 (14 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Names and Identifiers

IUPAC Name 4-chlorobenzene-1,2-diamine
INCHI InChI=1S/C6H7ClN2/c7-4-1-2-5(8)6(9)3-4/h1-3H,8-9H2
InChi Key BXIXXXYDDJVHDL-UHFFFAOYSA-N
Canonical SMILES C1=CC(=C(C=C1Cl)N)N
Isomeric SMILES C1=CC(=C(C=C1Cl)N)N
WGK Germany 3
RTECS SS8850000
PubChem CID 7263
UN Number 3143
Packing Group I
Molecular Weight 142.59
Beilstein 508472
Reaxy-Rn 508472

Certificates

Certificate of Analysis(COA)

Enter Lot Number to search for COA:

To view the certificate results,please click on a Lot number.For Lot numbers from past orders,please use our order status section

12 results found

Lot NumberCertificate TypeDateItem
C2323547Certificate of AnalysisMar 06, 2023 C122655
C2323550Certificate of AnalysisMar 06, 2023 C122655
C2323571Certificate of AnalysisMar 06, 2023 C122655
C2323574Certificate of AnalysisMar 06, 2023 C122655
C2323641Certificate of AnalysisMar 06, 2023 C122655
C2323642Certificate of AnalysisMar 06, 2023 C122655
F23061398Certificate of AnalysisMar 06, 2023 C122655
G2308178Certificate of AnalysisMar 06, 2023 C122655
F23061330Certificate of AnalysisJun 11, 2022 C122655
G2220483Certificate of AnalysisJun 11, 2022 C122655
G2220484Certificate of AnalysisJun 11, 2022 C122655
G2220485Certificate of AnalysisJun 11, 2022 C122655

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Chemical and Physical Properties

SolubilitySlightly soluble in water; Soluble in Benzene; Very slightly soluble in Ether,Ethanol
Sensitivityair sensitive
Melt Point(°C)70-73 °C

Safety and Hazards(GHS)

Pictogram(s) GHS08,   GHS07
Signal Warning
Hazard Statements

H315:Causes skin irritation

H319:Causes serious eye irritation

H335:May cause respiratory irritation

H351:Suspected of causing cancer

H302:Harmful if swallowed

Precautionary Statements

P261:Avoid breathing dust/fume/gas/mist/vapors/spray.

P305+P351+P338:IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses if present and easy to do - continue rinsing.

P280:Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352:IF ON SKIN: wash with plenty of water.

P321:Specific treatment (see ... on this label).

P405:Store locked up.

P501:Dispose of contents/container to ...

P264:Wash hands [and …] thoroughly after handling.

P271:Use only outdoors or in a well-ventilated area.

P270:Do not eat, drink or smoke when using this product.

P304+P340:IF INHALED: Remove person to fresh air and keep comfortable for breathing.

P403+P233:Store in a well-ventilated place. Keep container tightly closed.

P362+P364:Take off contaminated clothing and wash it before reuse.

P330:Rinse mouth.

P203:Obtain, read and follow all safety instructions before use.

P264+P265:Wash hands [and …] thoroughly after handling. Do not touch eyes.

P301+P317:IF SWALLOWED: Get medical help.

P318:if exposed or concerned, get medical advice.

P337+P317:If eye irritation persists: Get medical help.

P332+P317:If skin irritation occurs: Get medical help.

P319:Get medical help if you feel unwell.

WGK Germany 3
RTECS SS8850000
Reaxy-Rn 508472
Class 6.1

Related Documents

Citations of This Product

1. Shouying Wu, Linping Zhang, Jianing Fan, Wei Wu, Bolin Ji, Xueling Feng, Bijia Wang, Yimeng Ma, Yi Zhong, Hong Xu, Zhiping Mao.  (2023)  Iron(III) complexes promote hydrogen peroxide activation for efficient degradation of dyeing wastewater.  COLORATION TECHNOLOGY,    (1):   [PMID:10648423]
2. Zhang Luping, Tu Xuewei, Han Weihang, Chen Liangchen, Chen Yutong, Zheng Hui.  (2023)  The Efficient CO2 Fixation Catalyzed by Fe-Based Catalyst for Synthesizing Benzimidazoles.  CATALYSIS LETTERS,  153  (11): (3383-3391).  [PMID:]

References

1. L Soler-Niedziela,X Shi,J Nath,T Ong.  (1991-01-01)  Studies on three structurally related phenylenediamines with the mouse micronucleus assay system..  Mutation research,  259  ((1)): (43-48).  [PMID:1703280]
2. A F McFee, P P Jauhar, K W Lowe, J T MacGregor, C M Wehr,.  (1989-01-01)  Assays of three carcinogen/non-carcinogen chemical pairs for in vivo induction of chromosome aberrations, sister chromatid exchanges and micronuclei..  Environmental and molecular mutagenesis,  14  ((4)): ( 207-220 ).  [PMID:2583129]
3. .  (1982-04-01)  4-Chloro-ortho-phenylenediamine and 4-chloro-meta-phenylenediamine..  IARC monographs on the evaluation of the carcinogenic risk of chemicals to humans,  27  (81-89).  [PMID:6955270]
4. W Suter,F Staedtler,F Poetter-Locher,T Swingler,L Wilson.  (1998-06-19)  4-Chloro-o-phenylenediamine: a 26-week oral (in feed) mutagenicity study in Big Blue mice..  Mutation research,  414  ((1-3)): (149-156).  [PMID:9630584]
5. Hiroshi Suzuki,Naohiro Ikeda,Kazuo Kobayashi,Yukari Terashima,Yasushi Shimada,Takayoshi Suzuki,Toshiyuki Hagiwara,Shigeki Hatakeyama,Koko Nagaoka,Junichi Yoshida,Yukiko Saito,Jin Tanaka,Makoto Hayashi.  (2005-05-19)  Evaluation of liver and peripheral blood micronucleus assays with 9 chemicals using young rats. A study by the Collaborative Study Group for the Micronucleus Test (CSGMT)/Japanese Environmental Mutagen Society (JEMS)-Mammalian Mutagenicity Study Group (MMS)..  Mutation research,  583  ((2)): (133-145).  [PMID:15899588]
6. Ilaria Massarelli,Marcello Imbriani,Alessio Coi,Marilena Saraceno,Niccolò Carli,Anna Maria Bianucci.  (2009-03-11)  Development of QSAR models for predicting hepatocarcinogenic toxicity of chemicals..  European journal of medicinal chemistry,  44  ((9)): (3658-3664).  [PMID:19272677]
7. .  (2011-08-19)  4-Chloro-o-phenylenediamine..  Report on carcinogens : carcinogen profiles,  12  (101-102).  [PMID:21850148]
8. Dalia M S A Salem,Mohammed A E Sallam,Trevena N M A Youssef.  (2019-03-18)  Synthesis of compounds having antimicrobial activity from alginate..  Bioorganic chemistry,  87  (103-111).  [PMID:30878809]
9. .  (2004-08-24)  4-Chloro-o-phenylenediamine..  Report on carcinogens : carcinogen profiles,  10  (59-59).  [PMID:15320323]
10. .  (2004-01-01)  4-Chloro-o-phenylenediamine..  Report on carcinogens : carcinogen profiles,  11  (III58-III59).  [PMID:21089830]
11. Shouying Wu, Linping Zhang, Jianing Fan, Wei Wu, Bolin Ji, Xueling Feng, Bijia Wang, Yimeng Ma, Yi Zhong, Hong Xu, Zhiping Mao.  (2023)  Iron(III) complexes promote hydrogen peroxide activation for efficient degradation of dyeing wastewater.  COLORATION TECHNOLOGY,    (1):   [PMID:10648423]
12. Zhang Luping, Tu Xuewei, Han Weihang, Chen Liangchen, Chen Yutong, Zheng Hui.  (2023)  The Efficient CO2 Fixation Catalyzed by Fe-Based Catalyst for Synthesizing Benzimidazoles.  CATALYSIS LETTERS,  153  (11): (3383-3391).  [PMID:]

Solution Calculators