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2,4,4\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\'-Trifluoro-1,1\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\'-biphenyl


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2,4,4'-Trifluoro-1,1'-biphenyl ≥95%

Supplier: AOBChem USA
Description: 2,4,4'-Trifluoro-1,1'-biphenyl ≥95%

Image Unavailable-77368-564

2,4,4',5-Tetrafluoro-1,1'-biphenyl ≥97%

Supplier: AOBChem USA
Description: 2,4,4',5-Tetrafluoro-1,1'-biphenyl ≥97%

Product Image-101927-590

Biphenyl-2,4,4'-triamine

Catalog Number: (101927-590)
Supplier: Matrix Scientific
Description: Matrix Scientific Part Number: 064383-500MG , MDL Number: MFCD11053013
Image Unavailable-AAAL11961-14

1,3-Di-tert-butyltoluene 98+%

Catalog Number: (AAAL11961-14)
Supplier: Thermo Scientific Chemicals
Description: . Grade:98+, Melting Point C31-32*. Boiling Point C:243-244*. C15H24. 15181-11-0.

SDS Certificates


Image Unavailable-77131-848

Human Recombinant PSGL-1/CD162 Protein (from HEK293 cells)

Catalog Number: (77131-848)
Supplier: Prosci
Description: Human Recombinant PSGL-1/CD162 Protein (from HEK293 cells)
Image Unavailable-TCD3414-25G

1,3-Di-tert-butyltoluene ≥98.0%

Supplier: TCI America
Description: CAS Number: 15181-11-0
MDL Number: MFCD00026300
Molecular Formula: C15H24
Molecular Weight: 204.36
Purity/Analysis Method: >98.0% (GC)
Form: Crystal
Boiling point (°C): 244
Flash Point (°C): 91
Freezing point (°C): 30

SDS Certificates

Image Unavailable-TCC0254-500G

Monuron (N-(4-chlorophenyl)-N',N'-dimethylurea) ≥95.0% (by HPLC, total nitrogen)

Supplier: TCI America
Description: CAS Number: 150-68-5
MDL Number: MFCD00018556
Molecular Formula: C9H11ClN2O
Molecular Weight: 198.65
Purity/Analysis Method: >95.0% (HPLC,N)
Form: Crystal
Melting point (°C): 173
Lambda max.: 244 nm (H2O)

SDS

Image Unavailable-AAAL07743-09

3,3',5,5'-Tetra-tert-butyl-4,4'-diphenoquinone ≥98%

Supplier: Thermo Scientific Chemicals
Description: . Grade:98+, Melting Point C242-244*. Boiling Point C:NA. C28H40O2. 2455-14-3.

SDS Certificates

Image Unavailable-BT225525-100G

3-Chloroaniline ≥99%

Supplier: BeanTown Chemical
Description: CAS: 108-42-9; EC No: 203-581-0; MDL No: MFCD00007765; RTECS: BX0350000 UN No: UN2019; Haz Class: 6.1; Packing Group: II Liquid; Molecular Formula: C6H6ClN; MW: 127.57 Melting Point: -10°; Boiling Point: 95-96°/11 mmHg; Flash point: 118°C (244°F) Density (g/mL): 1.206; Refractive Index: 1.594

SDS

Product Image-76072-058

Anti-AQP11 Rabbit Polyclonal Antibody

Catalog Number: (76072-058)
Supplier: Prosci
Description: For WB starting dilution is: 1:2000 For FACS starting dilution is: 1:10~50
Image Unavailable-10479-136

Anti-TCRP1 Rabbit Polyclonal Antibody (Cy5.5®)

Catalog Number: (10479-136)
Supplier: Bioss
Description: FAM168A is a 244 amino acid protein that exists as three alternatively spliced isoforms and is encoded by a gene that maps to human chromosome 11, which makes up around 4% of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and ∫ thalassemia are caused by HBB gene mutations. Wilms' tumors, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11.
Image Unavailable-10479-616

Anti-FAM160B1 Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

Catalog Number: (10479-616)
Supplier: Bioss
Description: FAM168A is a 244 amino acid protein that exists as three alternatively spliced isoforms and is encoded by a gene that maps to human chromosome 11, which makes up around 4% of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and ∫ thalassemia are caused by HBB gene mutations. Wilms' tumors, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11.
Image Unavailable-76108-358

Anti-FAM160B1 Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Catalog Number: (76108-358)
Supplier: Bioss
Description: FAM168A is a 244 amino acid protein that exists as three alternatively spliced isoforms and is encoded by a gene that maps to human chromosome 11, which makes up around 4% of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and thalassemia are caused by HBB gene mutations. Wilms' tumors, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11.
Image Unavailable-76108-360

Anti-FAM160B1 Rabbit Polyclonal Antibody (Alexa Fluor® 750)

Catalog Number: (76108-360)
Supplier: Bioss
Description: FAM168A is a 244 amino acid protein that exists as three alternatively spliced isoforms and is encoded by a gene that maps to human chromosome 11, which makes up around 4% of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and thalassemia are caused by HBB gene mutations. Wilms' tumors, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11.
Image Unavailable-10479-142

Anti-TCRP1 Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

Catalog Number: (10479-142)
Supplier: Bioss
Description: FAM168A is a 244 amino acid protein that exists as three alternatively spliced isoforms and is encoded by a gene that maps to human chromosome 11, which makes up around 4% of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and ∫ thalassemia are caused by HBB gene mutations. Wilms' tumors, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11.
Image Unavailable-10479-440

Anti-FAM160B1 Rabbit Polyclonal Antibody (Cy5®)

Catalog Number: (10479-440)
Supplier: Bioss
Description: FAM168A is a 244 amino acid protein that exists as three alternatively spliced isoforms and is encoded by a gene that maps to human chromosome 11, which makes up around 4% of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and ∫ thalassemia are caused by HBB gene mutations. Wilms' tumors, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11.
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Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the call is still displayed and you need assistance, please call us at 1-800-932-5000.
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