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(2S,2'S)-2,2'-(Hexadecanedioylbis(azanediyl))dipentanedioic+acid


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Supplier:  Matrix Scientific
MSDS SDS

Supplier:  Bioss
Description:   C9orf16 (chromosome 9 open reading frame 16) is an 83 amino acid protein that belongs to the UPF0184 (EST00098) family and is encoded by a gene that maps to human chromosome 9q34.11. Chromosome 9 consists of about 145 million bases, represents 4% of the human genome and encodes nearly 900 genes. Thought to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias.

Supplier:  Bioss
Description:   C9orf23 (chromosome 9 open reading frame 23) is a 163 amino acid protein that belongs to the histone-like Alba family and is encoded by a gene that maps to human chromosome 9p13.3. Chromosome 9 consists of about 145 million bases, represents 4% of the human genome and encodes nearly 900 genes. Thought to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias.

Supplier:  Bioss
Description:   C9orf142 (chromosome 9 open reading frame 142) is a 204 amino acid protein that exists as two alternatively spliced isoforms. The gene encoding C9orf142 maps to human chromosome 9q34.3. Chromosome 9 consists of about 145 million bases, represents 4% of the human genome and encodes nearly 900 genes. Thought to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias.
Supplier:  AMBEED, INC
Description:   (2S,3S)-2-Amino-3-methyl-N-(2-morpholinoethyl)pentanamide ≥97%
New Product

Supplier:  Matrix Scientific
MSDS SDS

Supplier:  Bioss
Description:   C9orf140 (chromosome 9 open reading frame 140), also known as TS/MDEP (tumor specificity and mitosis phase-dependent expression protein) or p42.3, is a 394 amino acid nuclear and cytoplasmic protein encoded by a gene that maps to human chromosome 9q34.3. Chromosome 9 consists of about 145 million bases, represents 4% of the human genome and encodes nearly 900 genes. Thought to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias.
Catalog Number: (76822-292)

Supplier:  AMBEED, INC
Description:   (1S,2S)-2-(Benzylamino)cyclohexanol, Purity: 97%, CAS Number: 322407-34-1, Appearance: White to off-white solid, Storage: Keep in dark place, Inert atmosphere, 2-8C, Size: 5G
Supplier:  AMBEED, INC
Description:   (2S)-2-Amino-2-cyclopropylethan-1-ol hydrochloride ≥95%
New Product
Supplier:  AMBEED, INC
Description:   (2S,4R)-tert-Butyl 4-hydroxy-2-methylpyrrolidine-1-carboxylate, Purity: 95%, CAS Number: 114676-61-8, Appearance: White to Yellow Solid, Storage: Sealed in dry, 2-8C, Size: 5G
Supplier:  AMBEED, INC
Description:   (1S,2S,4R)-1-Methyl-2,4-di(prop-1-en-2-yl)-1-vinylcyclohexane ≥98%
New Product
Supplier:  AMBEED, INC
Description:   (2S,4S)-1-Benzyl 2-methyl 4-aminopyrrolidine-1,2-dicarboxylate hydrochloride, Purity: 95%, CAS number: 1515919-15-9, Appearance: Solid, Storage: Inert atmosphere, 2-8C, Size: 25G
Supplier:  TCI America
Description:   CAS Number: 19132-06-0
MDL Number: MFCD00063648
Molecular Formula: C4H10O2
Molecular Weight: 90.12
Purity/Analysis Method: >97.0% (GC)
Form: Clear Liquid
Boiling point (°C): 182
Flash Point (°C): 85
Freezing point (°C): 17
Specific Gravity (20/20): 0.99
Specific rotation [a]20/D: 13.5 deg (neat)
MSDS SDS
Supplier:  AMBEED, INC
Description:   tert-Butyl ((1S,2S)-2-hydroxycyclopentyl)carbamate, Purity: 99%, CAS Number: 145106-43-0, Appearance: Solid or liquid, Storage: Keep in dark place, Sealed in dry, 2-8C, Size: 25G
Supplier:  AMBEED, INC
Description:   (1S,2S)-2-(Diphenylphosphino)cyclohexanamine, Purity: 98%, CAS number: 452304-63-1, Appearance: Form: solid, Storage: Keep in dark place, Inert atmosphere, Room temperature, Size: 1G
Supplier:  TCI America
Description:   CAS Number: 29841-69-8
MDL Number: MFCD00082751
Molecular Formula: C14H16N2
Molecular Weight: 212.30
Purity/Analysis Method: >98.0% (GC,T)
Form: Crystal
Melting point (°C): 83
Specific rotation [a]20/D: -103 deg (C=1, EtOH)
MSDS SDS
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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.
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.
This product is marked as restricted and can only be purchased by approved Shipping Accounts. If you need further assistance, email VWR Regulatory Department at Regulatory_Affairs@vwr.com
-Additional Documentation May be needed to purchase this item. A VWR representative will contact you if needed.
This product has been blocked by your organization. Please contact your purchasing department for more information.
The original product is no longer available. The replacement shown is available.
This product is no longer available. Alternatives may be available by searching with the VWR Catalog Number listed above. If you need further assistance, please call VWR Customer Service at 1-800-932-5000.
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