Tel:
Email:

Phosphoramidites

  1. Home
  2. Products
  3. RNA Synthesis Reagents
  4. Phosphoramidites
2'-Modified Phosphoramidites
(549/549) 2'-Phosphoramidites
(27/27) 3'-Modified Phosphoramidites
(201/201) 5'-Modified Phosphoramidites
(34/34) Arabino Phosphoramidites
(24/24) Base Protected Phosphoramidites (435/435) Dye Phosphoramidites
(63/63) Label Phosphoramidites
(81/81) Linker Phosphoramidites
(97/97) Other Phosphoramidites
(94/94) PMO Phosphoramidates and Derivatives (33/33) PseudoUridine Phosphoramidite
(12/12) Reverse Phosphoramidites
(25/25) Spacer Phosphoramidites
(24/24)
Backbone
Modification
Base Type
Filtered by
Clear All

12-(Trifluoroacetylamino)-hexyl-(2-cyanoethyl)-(N,N-diisopropyl)-phosphoramidite

Description: 12-(Trifluoroacetylamino)-hexyl-(2-cyanoethyl)-(N,N-diisopropyl)-phosphoramidite is a phosphoramidite derivative used in oligonucleotide synthesis. It contains a hexyl chain modified with a trifluoroacetyl group and a cyanoethyl protecting group attached to a phosphoramidite backbone, facilitating efficient coupling reactions during solid-phase synthesis.
CAT: BRP-00773
CAS: 2087458-61-3
Molecular Formula: C23H43F3N3O3P
Molecular Weight: 497.58
Purity: ≥95%
Size Price Stock Quantity
-- -- --
Inquiry   
InChIKey: UOXSQLQMSFUIRH-UHFFFAOYSA-N
CanonicalSMILES: N#CCCOP(OCCCCCCCCCCCCNC(=O)C(F)(F)F)N(C(C)C)C(C)C
IUPAC Name: 2-cyanoethyl (12-(2,2,2-trifluoroacetamido)dodecyl) diisopropylphosphoramidite
InChI: InChI=1S/C23H43F3N3O3P/c1-20(2)29(21(3)4)33(32-19-15-16-27)31-18-14-12-10-8-6-5-7-9-11-13-17-28-22(30)23(24,25)26/h20-21H,5-15,17-19H2,1-4H3,(H,28,30)
Synonyms: 5'-Amino-Modifier C12-TFA phosphoramidite; Phosphoramidous acid, N,N-bis(1-methylethyl)-, 2-cyanoethyl 12-[(2,2,2-trifluoroacetyl)amino]dodecyl ester; 2-Cyanoethyl 12-[(2,2,2-trifluoroacetyl)amino]dodecyl N,N-bis(1-methylethyl)phosphoramidite; TFA-Amino C-12 CED phosphoramidite; 5'-Amino-Modifier C12-TFA

GalNAc-Cluster-HHA-CE Phosphoramidite

Description: GalNAc-Cluster-HHA-CE Phosphoramidite is a specialized compound utilized in oligonucleotide synthesis. It contains N-acetylgalactosamine clusters and a glycan-binding unit (HHA-CE), enabling the study of glycan-protein interactions, crucial in glycobiology and drug development.
CAT: BRP-00784
CAS: 2550328-16-8
Molecular Formula: C93H155N10O43P
Molecular Weight: 2132.24
Purity: ≥98%
Appearance: White solid
Size Price Stock Quantity
-- -- --
Inquiry   
Storage: Store at 2-8 °C
InChIKey: YBEYXGGMLIQBIC-AKUCVXOZSA-N
CanonicalSMILES: CC(C)N(C(C)C)P(OCCCCCCNC(=O)C(CCCCNC(=O)COCCOCCOCCOC1C(C(C(C(O1)COC(=O)C)OC(=O)C)OC(=O)C)NC(=O)C)NC(=O)C(CCCCNC(=O)COCCOCCOCCOC2C(C(C(C(O2)COC(=O)C)OC(=O)C)OC(=O)C)NC(=O)C)NC(=O)COCCOCCOCCOC3C(C(C(C(O3)COC(=O)C)OC(=O)C)OC(=O)C)NC(=O)C)OCCC#N
IUPAC Name: [(2R,3R,4R,5R,6R)-5-acetamido-6-[2-[2-[2-[2-[[(5S)-5-[[2-[2-[2-[2-[(2R,3R,4R,5R,6R)-3-acetamido-4,5-diacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxyethoxy]ethoxy]ethoxy]acetyl]amino]-6-[[(2R)-6-[[2-[2-[2-[2-[(2R,3R,4R,5R,6R)-3-acetamido-4,5-diacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxyethoxy]ethoxy]ethoxy]acetyl]amino]-1-[6-[2-cyanoethoxy-[di(propan-2-yl)amino]phosphanyl]oxyhexylamino]-1-oxohexan-2-yl]amino]-6-oxohexyl]amino]-2-oxoethoxy]ethoxy]ethoxy]ethoxy]-3,4-diacetyloxyoxan-2-yl]methyl acetate
InChI: InChI=1S/C93H155N10O43P/c1-58(2)103(59(3)4)147(137-33-25-28-94)136-32-24-18-17-21-31-97-89(119)72(26-19-22-29-95-77(116)55-127-43-40-121-34-37-124-46-49-130-91-80(98-60(5)104)86(141-69(14)113)83(138-66(11)110)74(144-91)52-133-63(8)107)102-90(120)73(101-79(118)57-129-45-42-123-36-39-126-48-51-132-93-82(100-62(7)106)88(143-71(16)115)85(140-68(13)112)76(146-93)54-135-65(10)109)27-20-23-30-96-78(117)56-128-44-41-122-35-38-125-47-50-131-92-81(99-61(6)105)87(142-70(15)114)84(139-67(12)111)75(145-92)53-134-64(9)108/h58-59,72-76,80-88,91-93H,17-27,29-57H2,1-16H3,(H,95,116)(H,96,117)(H,97,119)(H,98,104)(H,99,105)(H,100,106)(H,101,118)(H,102,120)/t72-,73+,74-,75-,76-,80-,81-,82-,83+,84+,85+,86-,87-,88-,91-,92-,93-,147?/m1/s1

DMT-LNA-5mC phosphoramidite

Description: DMT-LNA-5mC phosphoramidite is a modified phosphoramidite used in the synthesis of Locked Nucleic Acid (LNA) oligonucleotides. It features a 5-methylcytosine (5mC) base, a DMT (dimethoxytrityl) protecting group, and a phosphoramidite group. This modification increases the thermal stability and binding affinity of the oligonucleotide, making it useful in antisense therapy, siRNA development, and molecular biology techniques.
CAT: BRP-00811
CAS: 1184723-53-2
Molecular Formula: C41H50N5O8P
Molecular Weight: 771.84
Purity: 98%
Size Price Stock Quantity
-- -- --
Inquiry   
Storage: Store at 2-8 °C, stored under nitrogen
InChIKey: UJUKPCINNDKWEN-ZRCIEBSPSA-N
CanonicalSMILES: CC1=CN(C(=O)N=C1N)C2C3C(C(O2)(CO3)COC(C4=CC=CC=C4)(C5=CC=C(C=C5)OC)C6=CC=C(C=C6)OC)OP(N(C(C)C)C(C)C)OCCC#N
IUPAC Name: 3-[[(1R,3R,4R,7S)-3-(4-amino-5-methyl-2-oxopyrimidin-1-yl)-1-[[bis(4-methoxyphenyl)-phenylmethoxy]methyl]-2,5-dioxabicyclo[2.2.1]heptan-7-yl]oxy-[di(propan-2-yl)amino]phosphanyl]oxypropanenitrile
InChI: InChI=1S/C41H50N5O8P/c1-27(2)46(28(3)4)55(52-23-11-22-42)54-36-35-38(45-24-29(5)37(43)44-39(45)47)53-40(36,25-50-35)26-51-41(30-12-9-8-10-13-30,31-14-18-33(48-6)19-15-31)32-16-20-34(49-7)21-17-32/h8-10,12-21,24,27-28,35-36,38H,11,23,25-26H2,1-7H3,(H2,43,44,47)/t35-,36+,38-,40-,55?/m1/s1
Synonyms: LNA-5-Me-C-CE Phosphoramidite; DMT-LNA-5mA phosphoramidite; 2(1H)-Pyrimidinone, 4-amino-1-[2,5-anhydro-4-C-[[bis(4-methoxyphenyl)phenylmethoxy]methyl]-3-O-[[bis(1-methylethyl)amino](2-cyanoethoxy)phosphino]-α-L-lyxofuranosyl]-5-methyl-; 4-Amino-1-[2,5-anhydro-4-C-[[bis(4-methoxyphenyl)phenylmethoxy]methyl]-3-O-[[bis(1-methylethyl)amino](2-cyanoethoxy)phosphino]-α-L-lyxofuranosyl]-5-methyl-2(1H)-pyrimidinone

DMT-LNA-G phosphoramidite

Description: DMT-LNA-G phosphoramidite is a modified phosphoramidite used in oligonucleotide synthesis, specifically for Locked Nucleic Acid (LNA) oligonucleotides. It contains a guanosine base modified with Locked Nucleic Acid (LNA) chemistry and a DMT (dimethoxytrityl) protecting group. This modification enhances the stability and binding affinity of the oligonucleotide to its complementary DNA or RNA strand. DMT-LNA-G phosphoramidite is commonly used in applications such as antisense therapy, PCR, and molecular diagnostics, where increased specificity and stability are required.
CAT: BRP-00812
CAS: 207131-17-7
Molecular Formula: C41H48N7O8P
Molecular Weight: 797.84
Purity: 98%
Size Price Stock Quantity
-- -- --
Inquiry   
Storage: Store at 2-8 °C, stored under nitrogen
InChIKey: FWLGFXLWSNDRLS-NVONNAQSSA-N
CanonicalSMILES: CC(C)N(C(C)C)P(OCCC#N)OC1C2C(OC1(CO2)COC(C3=CC=CC=C3)(C4=CC=C(C=C4)OC)C5=CC=C(C=C5)OC)N6C=NC7=C6N=C(NC7=O)N
IUPAC Name: 3-[[(1R,3R,4R,7S)-3-(2-amino-6-oxo-1H-purin-9-yl)-1-[[bis(4-methoxyphenyl)-phenylmethoxy]methyl]-2,5-dioxabicyclo[2.2.1]heptan-7-yl]oxy-[di(propan-2-yl)amino]phosphanyl]oxypropanenitrile
InChI: InChI=1S/C41H48N7O8P/c1-26(2)48(27(3)4)57(54-22-10-21-42)56-35-34-38(47-25-44-33-36(47)45-39(43)46-37(33)49)55-40(35,23-52-34)24-53-41(28-11-8-7-9-12-28,29-13-17-31(50-5)18-14-29)30-15-19-32(51-6)20-16-30/h7-9,11-20,25-27,34-35,38H,10,22-24H2,1-6H3,(H3,43,45,46,49)/t34-,35+,38-,40-,57?/m1/s1
Synonyms: Guanosine, 5'-O-[bis(4-methoxyphenyl)phenylmethyl]-2'-O,4'-C-methylene-, 3'-[2-cyanoethyl bis(1-methylethyl)phosphoramidite]; (1R,3R,4R,7S)-3-(2-Amino-6-oxo-1,6-dihydro-9H-purin-9-yl)-1-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-2,5-dioxabicyclo[2.2.1]heptan-7-yl (2-cyanoethyl) diisopropylphosphoramidite

LNA A(pac) amidite

Description: LNA A(pac) amidite is a modified phosphoramidite used in oligonucleotide synthesis, specifically for incorporating Locked Nucleic Acid (LNA) modifications into nucleic acid sequences. This modification involves attaching a phenoxyacetyl (pac) group to the adenine base of LNA. It is commonly used to enhance the binding affinity, stability, and specificity of oligonucleotides in various applications such as antisense therapy, PCR, and molecular diagnostics.
CAT: BRP-00813
Molecular Formula: C49H54N7O9P
Molecular Weight: 915.98
Purity: >98%
Appearance: Off-white solid
Size Price Stock Quantity
-- -- --
Inquiry   
Storage: Store at -20 °C
InChIKey: RHUYJRYFCPQBIE-LXTWGDFWSA-N
Solubility: Soluble in Acetonitrile, DMF
IUPAC Name: (1R,3R,4R,7S)-1-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-3-(6-(2-phenoxyacetamido)-9H-purin-9-yl)-2,5-dioxabicyclo[2.2.1]heptan-7-yl (2-cyanoethyl) diisopropylphosphoramidite
InChI: InChI=1S/C49H54N7O9P/c1-33(2)56(34(3)4)66(63-27-13-26-50)65-44-43-47(55-32-53-42-45(51-31-52-46(42)55)54-41(57)28-60-40-16-11-8-12-17-40)64-48(44,29-61-43)30-62-49(35-14-9-7-10-15-35,36-18-22-38(58-5)23-19-36)37-20-24-39(59-6)25-21-37/h7-12,14-25,31-34,43-44,47H,13,27-30H2,1-6H3,(H,51,52,54,57)/t43-,44+,47-,48-,66?/m1/s1
Synonyms: LNA A(pac) CE-Phosphoramidite; DMTr-LNA-A(pac)-3-CED-phosphoramidite

2'-OTFM U amidite

Description: 2'-OTFM U amidite is a modified phosphoramidite used in oligonucleotide synthesis, particularly for introducing 2'-O-trifluoromethyl (OTFM) modifications into RNA sequences. This modification involves adding a trifluoromethyl group to the 2'-position of uridine. It is utilized to enhance the stability and specificity of RNA molecules in various applications such as RNA interference, antisense therapy, and RNA structural studies.
CAT: BRP-00814
CAS: 869734-94-1
Molecular Formula: C40H46F3N4O9P
Molecular Weight: 814.79
Purity: >95%
Appearance: Off-white solid
Size Price Stock Quantity
-- -- --
Inquiry   
Storage: Store at -20 °C
InChIKey: AIVSTWHGYKADBY-FNMBQTMFSA-N
Solubility: Soluble in Acetonitrile, DMF
CanonicalSMILES: CC(C)N(C(C)C)P(OCCC#N)OC1C(OC(C1OC(F)(F)F)N2C=CC(=O)NC2=O)COC(C3=CC=CC=C3)(C4=CC=C(C=C4)OC)C5=CC=C(C=C5)OC
IUPAC Name: 3-[[(2R,3R,4R,5R)-2-[[bis(4-methoxyphenyl)-phenylmethoxy]methyl]-5-(2,4-dioxopyrimidin-1-yl)-4-(trifluoromethoxy)oxolan-3-yl]oxy-[di(propan-2-yl)amino]phosphanyl]oxypropanenitrile
InChI: InChI=1S/C40H46F3N4O9P/c1-26(2)47(27(3)4)57(53-24-10-22-44)56-35-33(54-37(36(35)55-40(41,42)43)46-23-21-34(48)45-38(46)49)25-52-39(28-11-8-7-9-12-28,29-13-17-31(50-5)18-14-29)30-15-19-32(51-6)20-16-30/h7-9,11-21,23,26-27,33,35-37H,10,24-25H2,1-6H3,(H,45,48,49)/t33-,35-,36-,37-,57?/m1/s1
Synonyms: Uridine, 5'-O-[bis(4-methoxyphenyl)phenylmethyl]-2'-O-(trifluoromethyl)-, 3'-[2-cyanoethyl bis(1-methylethyl)phosphoramidite]; (2R,3R,4R,5R)-2-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-4-(trifluoromethoxy)tetrahydrofuran-3-yl (2-cyanoethyl) diisopropylphosphoramidite

LNA G(iPr-pac) amidite

Description: LNA G(iPr-pac) amidite is a modified phosphoramidite used in oligonucleotide synthesis, specifically for incorporating Locked Nucleic Acid (LNA) modifications into nucleic acid sequences. This modification involves attaching an isopropylphenoxyacetyl (iPr-pac) group to the guanine base of LNA. It is commonly used to enhance the stability, specificity, and binding affinity of oligonucleotides in various applications such as antisense therapy, PCR, and molecular diagnostics.
CAT: BRP-00815
Molecular Formula: C52H60N7O10P
Molecular Weight: 974.06
Purity: >95%
Appearance: Off-white solid
Size Price Stock Quantity
-- -- --
Inquiry   
Storage: Store at -20 °C
InChIKey: FSLCFYFCVYNCAE-ZVOKJCSSSA-N
Solubility: Soluble in Acetonitrile, DMF
IUPAC Name: (1R,3R,4R,7S)-1-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-3-(2-(2-(4-isopropylphenoxy)acetamido)-6-oxo-1,6-dihydro-9H-purin-9-yl)-2,5-dioxabicyclo[2.2.1]heptan-7-yl (2-cyanoethyl) diisopropylphosphoramidite
InChI: InChI=1S/C52H60N7O10P/c1-33(2)36-15-21-42(22-16-36)64-29-43(60)55-50-56-47-44(48(61)57-50)54-32-58(47)49-45-46(69-70(67-28-12-27-53)59(34(3)4)35(5)6)51(68-49,30-65-45)31-66-52(37-13-10-9-11-14-37,38-17-23-40(62-7)24-18-38)39-19-25-41(63-8)26-20-39/h9-11,13-26,32-35,45-46,49H,12,28-31H2,1-8H3,(H2,55,56,57,60,61)/t45-,46+,49-,51-,70?/m1/s1
Synonyms: LNA G(iPr-pac) CE-Phosphoramidite; DMTr-LNA-G(iPr-pac)-3-CED-phosphoramidite

2'-OTFM C(Ac) amidite

Description: 2'-OTFM C(Ac) amidite is a modified phosphoramidite used in oligonucleotide synthesis to introduce 2'-O-trifluoromethyl (OTFM) modifications into RNA sequences, specifically targeting cytidine (C). This modification involves adding a trifluoromethyl group to the 2'-position of cytidine and acetylating the amino group of cytidine. It enhances the stability and specificity of RNA molecules and is commonly used in applications such as RNA interference, antisense therapy, and RNA structural studies.
CAT: BRP-00816
CAS: 869734-91-8
Molecular Formula: C42H49F3N5O9P
Molecular Weight: 855.85
Purity: >95%
Appearance: Off-white solid
Size Price Stock Quantity
-- -- --
Inquiry   
Storage: Store at -20 °C
InChIKey: VECFWZPFXRVLKY-HCIBFWJXSA-N
Solubility: Soluble in Acetonitrile, DMF
CanonicalSMILES: CC(C)N(C(C)C)P(OCCC#N)OC1C(OC(C1OC(F)(F)F)N2C=CC(=NC2=O)NC(=O)C)COC(C3=CC=CC=C3)(C4=CC=C(C=C4)OC)C5=CC=C(C=C5)OC
IUPAC Name: N-[1-[(2R,3R,4R,5R)-5-[[bis(4-methoxyphenyl)-phenylmethoxy]methyl]-4-[2-cyanoethoxy-[di(propan-2-yl)amino]phosphanyl]oxy-3-(trifluoromethoxy)oxolan-2-yl]-2-oxopyrimidin-4-yl]acetamide
InChI: InChI=1S/C42H49F3N5O9P/c1-27(2)50(28(3)4)60(56-25-11-23-46)59-37-35(57-39(38(37)58-42(43,44)45)49-24-22-36(47-29(5)51)48-40(49)52)26-55-41(30-12-9-8-10-13-30,31-14-18-33(53-6)19-15-31)32-16-20-34(54-7)21-17-32/h8-10,12-22,24,27-28,35,37-39H,11,25-26H2,1-7H3,(H,47,48,51,52)/t35-,37-,38-,39-,60?/m1/s1
Synonyms: Cytidine, N-acetyl-5'-O-[bis(4-methoxyphenyl)phenylmethyl]-2'-O-(trifluoromethyl)-, 3'-[2-cyanoethyl bis(1-methylethyl)phosphoramidite]; (2R,3R,4R,5R)-5-(4-acetamido-2-oxopyrimidin-1(2H)-yl)-2-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-4-(trifluoromethoxy)tetrahydrofuran-3-yl (2-cyanoethyl) diisopropylphosphoramidite; 2'-OTFM C(Ac) CE-Phosphoramidite

2'-OTFM C(Bz) amidite

Description: 2'-OTFM C(Bz) amidite is a modified phosphoramidite used in oligonucleotide synthesis to introduce 2'-O-trifluoromethyl (OTFM) modifications into RNA sequences, specifically targeting cytidine (C). This modification involves adding a trifluoromethyl group to the 2'-position of cytidine and benzoylating the amino group of cytidine. It enhances the stability and specificity of RNA molecules and is commonly used in applications such as RNA interference, antisense therapy, and RNA structural studies.
CAT: BRP-00817
Molecular Formula: C47H51F3N5O9P
Molecular Weight: 917.92
Purity: >95%
Appearance: Off-white solid
Size Price Stock Quantity
-- -- --
Inquiry   
Storage: Store at -20 °C
InChIKey: APWVCZQYEKTHIH-WKNHZCODSA-N
Solubility: Soluble in Acetonitrile, DMF
IUPAC Name: (2R,3R,4R,5R)-5-(4-benzamido-2-oxopyrimidin-1(2H)-yl)-2-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-4-(trifluoromethoxy)tetrahydrofuran-3-yl (2-cyanoethyl) diisopropylphosphoramidite
InChI: InChI=1S/C47H51F3N5O9P/c1-31(2)55(32(3)4)65(61-29-13-27-51)64-41-39(62-44(42(41)63-47(48,49)50)54-28-26-40(53-45(54)57)52-43(56)33-14-9-7-10-15-33)30-60-46(34-16-11-8-12-17-34,35-18-22-37(58-5)23-19-35)36-20-24-38(59-6)25-21-36/h7-12,14-26,28,31-32,39,41-42,44H,13,29-30H2,1-6H3,(H,52,53,56,57)/t39-,41-,42-,44-,65?/m1/s1
Synonyms: 2'-OTFM C(Bz) CE-Phosphoramidite

2'-OTFM G(iBu) amidite

Description: 2'-OTFM G(iBu) amidite is a modified phosphoramidite used in oligonucleotide synthesis to introduce 2'-O-trifluoromethyl (OTFM) modifications into RNA sequences, specifically targeting guanosine (G). This modification involves adding a trifluoromethyl group to the 2'-position of guanosine and attaching an isobutyl (iBu) group to the exocyclic amine of guanosine. It enhances the stability and specificity of RNA molecules and is commonly used in applications such as RNA interference, antisense therapy, and RNA structural studies.
CAT: BRP-00818
Molecular Formula: C45H53F3N7O9P
Molecular Weight: 923.93
Purity: >95%
Appearance: Off-white solid
Size Price Stock Quantity
-- -- --
Inquiry   
Storage: Store at -20 °C
InChIKey: YINYCQLAYPBOSI-SDLFASLNSA-N
Solubility: Soluble in Acetonitrile, DMF
CanonicalSMILES: CC(C)C(=O)NC1=NC2=C(C(=O)N1)N=CN2C3C(C(C(O3)COC(C4=CC=CC=C4)(C5=CC=C(C=C5)OC)C6=CC=C(C=C6)OC)OP(N(C(C)C)C(C)C)OCCC#N)OC(F)(F)F
IUPAC Name: N-[9-[(2R,3R,4R,5R)-5-[[bis(4-methoxyphenyl)-phenylmethoxy]methyl]-4-[2-cyanoethoxy-[di(propan-2-yl)amino]phosphanyl]oxy-3-(trifluoromethoxy)oxolan-2-yl]-6-oxo-1H-purin-2-yl]-2-methylpropanamide
InChI: InChI=1S/C45H53F3N7O9P/c1-27(2)40(56)52-43-51-39-36(41(57)53-43)50-26-54(39)42-38(63-45(46,47)48)37(64-65(61-24-12-23-49)55(28(3)4)29(5)6)35(62-42)25-60-44(30-13-10-9-11-14-30,31-15-19-33(58-7)20-16-31)32-17-21-34(59-8)22-18-32/h9-11,13-22,26-29,35,37-38,42H,12,24-25H2,1-8H3,(H2,51,52,53,56,57)/t35-,37-,38-,42-,65?/m1/s1
Synonyms: (2R,3R,4R,5R)-2-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-5-(2-isobutyramido-6-oxo-1,6-dihydro-9H-purin-9-yl)-4-(trifluoromethoxy)tetrahydrofuran-3-yl (2-cyanoethyl) diisopropylphosphoramidite; 2'-OTFM G(iBu) CE-Phosphoramidite

2'-OMe C(Ac) Me-amidite

Description: 2'-OMe C(Ac) Me-amidite is a modified phosphoramidite used in oligonucleotide synthesis, particularly for introducing 2'-O-methyl (2'-OMe) modifications into RNA sequences, specifically targeting cytidine (C). This modification involves adding a methyl group to the 2'-position of cytidine and acetylating the amino group of cytidine. It enhances the stability and specificity of RNA molecules and is commonly used in applications such as RNA interference, antisense therapy, and RNA structural studies.
CAT: BRP-00821
CAS: 205116-62-7
Molecular Formula: C40H51N4O8P
Molecular Weight: 746.84
Purity: >95%
Appearance: Off-white solid
Size Price Stock Quantity
-- -- --
Inquiry   
Storage: Store at -20 °C
InChIKey: QRMLMMQHOYHYLD-GFIGKZKCSA-N
Solubility: Soluble in Acetonitrile, DMF
CanonicalSMILES: O=C1N=C(C=CN1C2OC(COC(C=3C=CC=CC3)(C4=CC=C(OC)C=C4)C5=CC=C(OC)C=C5)C(OP(N(C(C)C)C(C)C)C)C2OC)NC(=O)C
IUPAC Name: N-(1-((2R,3R,4R,5R)-5-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-4-(((diisopropylamino)(methyl)phosphaneyl)oxy)-3-methoxytetrahydrofuran-2-yl)-2-oxo-1,2-dihydropyrimidin-4-yl)acetamide
InChI: InChI=1S/C40H51N4O8P/c1-26(2)44(27(3)4)53(9)52-36-34(51-38(37(36)49-8)43-24-23-35(41-28(5)45)42-39(43)46)25-50-40(29-13-11-10-12-14-29,30-15-19-32(47-6)20-16-30)31-17-21-33(48-7)22-18-31/h10-24,26-27,34,36-38H,25H2,1-9H3,(H,41,42,45,46)/t34-,36-,37-,38-,53?/m1/s1
Synonyms: Cytidine, N-acetyl-5'-O-[bis(4-methoxyphenyl)phenylmethyl]-2'-O-methyl-, 3'-[P-methyl-N,N-bis(1-methylethyl)phosphonamidite]; 5'-O-DMTr-2'-OMe-C(Ac)-3'-O-[P-methyl-(N,N-diisopropyl)]-Phosphoramidite; N4-acetyl-5'-O-(4,4'-dimethoxytrityl)-2'-OMe-C-3'-O-[P-methyl-(N,N-diisopropyl)]-Phosphoramidite; 2'-O-Methyl Cytidine (n-acetyl) p-methyl phosphonamidite; 5'-O-DMTr-2'-OMe-C(Ac) methyl phosphonamidite

2'-OMe A(Bz) Me-amidite

Description: 2'-OMe A(Bz) Me-amidite is a modified phosphoramidite used in oligonucleotide synthesis to introduce 2'-O-methyl (2'-OMe) modifications into RNA sequences, specifically targeting adenosine (A). This modification involves adding a methyl group to the 2'-position of adenosine and benzoylating the amino group of adenosine. It enhances the stability and specificity of RNA molecules and is commonly used in applications such as RNA interference, antisense therapy, and RNA structural studies.
CAT: BRP-00822
CAS: 158691-23-7
Molecular Formula: C46H53N6O7P
Molecular Weight: 832.94
Purity: >95%
Appearance: Off-white solid
Size Price Stock Quantity
-- -- --
Inquiry   
Storage: Store at -20 °C
InChIKey: GICXOURJNDWAPG-NSWJMSGMSA-N
Solubility: Soluble in Acetonitrile, DMF
CanonicalSMILES: O=C(NC1=NC=NC2=C1N=CN2C3OC(COC(C=4C=CC=CC4)(C5=CC=C(OC)C=C5)C6=CC=C(OC)C=C6)C(OP(N(C(C)C)C(C)C)C)C3OC)C=7C=CC=CC7
IUPAC Name: N-(9-((2R,3R,4R,5R)-5-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-4-(((diisopropylamino)(methyl)phosphaneyl)oxy)-3-methoxytetrahydrofuran-2-yl)-9H-purin-6-yl)benzamide
InChI: InChI=1S/C46H53N6O7P/c1-30(2)52(31(3)4)60(8)59-40-38(58-45(41(40)56-7)51-29-49-39-42(47-28-48-43(39)51)50-44(53)32-15-11-9-12-16-32)27-57-46(33-17-13-10-14-18-33,34-19-23-36(54-5)24-20-34)35-21-25-37(55-6)26-22-35/h9-26,28-31,38,40-41,45H,27H2,1-8H3,(H,47,48,50,53)/t38-,40-,41-,45-,60?/m1/s1
Synonyms: Adenosine, N-benzoyl-5'-O-[bis(4-methoxyphenyl)phenylmethyl]-2'-O-methyl-, 3'-[P-methyl-N,N-bis(1-methylethyl)phosphonamidite]; 5'-O-DMTr-2'-OMe-A(Bz)-3'-O-[P-methyl-(N,N-diisopropyl)]-Phosphoramidite; N6-benzoyl-5'-O-(4,4'-dimethoxytrityl)-2'-OMe-adenosine-3'-O-[P-methyl-(N,N-diisopropyl)]-Phosphoramidite; 2'-O-Methyl Adenosine (n-bz) p-methyl phosphonamidite; 5'-O-DMTr-2'-OMe-A(Bz) methyl phosphonamidite

2'-OMe G(iBu) Me-amidite

Description: 2'-OMe G(iBu) Me-amidite is a modified phosphoramidite used in oligonucleotide synthesis to introduce 2'-O-methyl (2'-OMe) modifications into RNA sequences, specifically targeting guanosine (G). This modification involves adding a methyl group to the 2'-position of guanosine and attaching an isobutyl (iBu) group to the exocyclic amine of guanosine. It enhances the stability and specificity of RNA molecules and is commonly used in applications such as RNA interference, antisense therapy, and RNA structural studies.
CAT: BRP-00823
CAS: 191786-63-7
Molecular Formula: C43H55N6O8P
Molecular Weight: 814.92
Purity: >95%
Appearance: Off-white solid
Size Price Stock Quantity
-- -- --
Inquiry   
Storage: Store at -20 °C
InChIKey: JAVHPGCWDJVLLN-BSQJSOGMSA-N
Solubility: Soluble in Acetonitrile, DMF
CanonicalSMILES: O=C1N=C(NC(=O)C(C)C)NC2=C1N=CN2C3OC(COC(C=4C=CC=CC4)(C5=CC=C(OC)C=C5)C6=CC=C(OC)C=C6)C(OP(N(C(C)C)C(C)C)C)C3OC
IUPAC Name: N-(9-((2R,3R,4R,5R)-5-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-4-(((diisopropylamino)(methyl)phosphaneyl)oxy)-3-methoxytetrahydrofuran-2-yl)-6-oxo-6,9-dihydro-1H-purin-2-yl)isobutyramide
InChI: InChI=1S/C43H55N6O8P/c1-26(2)39(50)46-42-45-38-35(40(51)47-42)44-25-48(38)41-37(54-9)36(57-58(10)49(27(3)4)28(5)6)34(56-41)24-55-43(29-14-12-11-13-15-29,30-16-20-32(52-7)21-17-30)31-18-22-33(53-8)23-19-31/h11-23,25-28,34,36-37,41H,24H2,1-10H3,(H2,45,46,47,50,51)/t34-,36-,37-,41-,58?/m1/s1
Synonyms: Guanosine, 5'-O-[bis(4-methoxyphenyl)phenylmethyl]-2'-O-methyl-N-(2-methyl-1-oxopropyl)-, 3'-[P-methyl-N,N-bis(1-methylethyl)phosphonamidite]; 5'-O-DMTr-2'-OMe-G(iBu)-3'-O-[P-methyl-(N,N-diisopropyl)]-Phosphoramidite; N2-Isobutyryl-5'-O-(4,4'-dimethoxytrityl)-2'-OMe-G-3'-O-[P-methyl-(N,N-diisopropyl)]-Phosphoramidite; 2'-O-Methyl Guanosine (n-ibu) p-methyl phosphonamidite; 5'-O-DMTr-2'-OMe-G(iBu) methyl phosphonamidite

MMTr C7 amine amidite

Description: MMTr C7 amine amidite is a linker phosphoramidite used in oligonucleotide synthesis. This compound serves as a linker during solid-phase oligonucleotide synthesis, allowing for the attachment of nucleotide building blocks to a growing oligonucleotide chain. MMTr C7 amine amidite plays a crucial role in the efficient and controlled synthesis of modified oligonucleotides for various applications in molecular biology and biotechnology.
CAT: BRP-00824
Molecular Formula: C36H50N3O3P
Molecular Weight: 603.79
Purity: >95%
Appearance: Light-yellow oily matter
Size Price Stock Quantity
-- -- --
Inquiry   
Storage: Store at -20 °C
InChIKey: SESSADZGYXHMSJ-UHFFFAOYSA-N
Solubility: Soluble in Acetonitrile, DMF
CanonicalSMILES: CC(C)N(C(C)C)P(OCCCCCCCNC(C1=CC=CC=C1)(C2=CC=CC=C2)C3=CC=C(C=C3)OC)OCCC#N
IUPAC Name: 3-[[di(propan-2-yl)amino]-[7-[[(4-methoxyphenyl)-diphenylmethyl]amino]heptoxy]phosphanyl]oxypropanenitrile
InChI: InChI=1S/C36H50N3O3P/c1-30(2)39(31(3)4)43(42-29-17-26-37)41-28-16-8-6-7-15-27-38-36(32-18-11-9-12-19-32,33-20-13-10-14-21-33)34-22-24-35(40-5)25-23-34/h9-14,18-25,30-31,38H,6-8,15-17,27-29H2,1-5H3
Synonyms: 2-cyanoethyl (7-(((4-methoxyphenyl)diphenylmethyl)amino)heptyl) diisopropylphosphoramidite; NHMMTr-C7 Phosphoramidite; Monomethoxytrityl-heptylamine-linker Phosphoramidite

MMTr C5 amine amidite

Description: MMTr C5 amine amidite is a linker phosphoramidite used in oligonucleotide synthesis. This compound serves as a linker during solid-phase oligonucleotide synthesis, allowing the attachment of nucleotide building blocks to a growing oligonucleotide chain. MMTr C5 amine amidite plays a crucial role in the efficient and controlled synthesis of modified oligonucleotides for various applications in molecular biology and biotechnology.
CAT: BRP-00825
CAS: 178811-39-7
Molecular Formula: C34H46N3O3P
Molecular Weight: 575.73
Purity: >95%
Appearance: Light-yellow oily matter
Size Price Stock Quantity
-- -- --
Inquiry   
Storage: Store at -20 °C
InChIKey: QKLNHYFSRTYCRA-UHFFFAOYSA-N
Solubility: Soluble in Acetonitrile, DMF
CanonicalSMILES: CC(C)N(C(C)C)P(OCCC#N)OCCCCCNC(C1=CC=C(OC)C=C1)(C2=CC=CC=C2)C3=CC=CC=C3
IUPAC Name: 2-cyanoethyl (5-(((4-methoxyphenyl)diphenylmethyl)amino)pentyl) diisopropylphosphoramidite
InChI: InChI=1S/C34H46N3O3P/c1-28(2)37(29(3)4)41(40-27-15-24-35)39-26-14-8-13-25-36-34(30-16-9-6-10-17-30,31-18-11-7-12-19-31)32-20-22-33(38-5)23-21-32/h6-7,9-12,16-23,28-29,36H,8,13-15,25-27H2,1-5H3
Synonyms: NHMMTr-C5 Phosphoramidite; Monomethoxytrityl-pentylamine-linker Phosphoramidite

MMTr C4 amine amidite

Description: MMTr C4 amine amidite is a linker phosphoramidite used in oligonucleotide synthesis. This compound serves as a linker during solid-phase oligonucleotide synthesis, facilitating the attachment of nucleotide building blocks to a growing oligonucleotide chain. MMTr C4 amine amidite is essential for the controlled synthesis of modified oligonucleotides for various applications in molecular biology and biotechnology.
CAT: BRP-00826
CAS: 178811-38-6
Molecular Formula: C33H44N3O3P
Molecular Weight: 561.71
Purity: >95%
Appearance: Light-yellow oily matter
Size Price Stock Quantity
-- -- --
Inquiry   
Storage: Store at -20 °C
InChIKey: LVYNYJLDPZLYCP-UHFFFAOYSA-N
Solubility: Soluble in Acetonitrile, DMF
CanonicalSMILES: CC(C)N(C(C)C)P(OCCC#N)OCCCCNC(C1=CC=C(OC)C=C1)(C2=CC=CC=C2)C3=CC=CC=C3
IUPAC Name: 2-cyanoethyl (4-(((4-methoxyphenyl)diphenylmethyl)amino)butyl) diisopropylphosphoramidite
InChI: InChI=1S/C33H44N3O3P/c1-27(2)36(28(3)4)40(39-26-14-23-34)38-25-13-12-24-35-33(29-15-8-6-9-16-29,30-17-10-7-11-18-30)31-19-21-32(37-5)22-20-31/h6-11,15-22,27-28,35H,12-14,24-26H2,1-5H3
Synonyms: NHMMTr-C4 Phosphoramidite; Monomethoxytrityl-butylamine-linker Phosphoramidite

MMTr C2 amine amidite

Description: MMTr C2 amine amidite is a linker phosphoramidite used in oligonucleotide synthesis. This compound serves as a linker during solid-phase oligonucleotide synthesis, enabling the attachment of nucleotide building blocks to a growing oligonucleotide chain. MMTr C2 amine amidite is crucial for the controlled synthesis of modified oligonucleotides for various applications in molecular biology and biotechnology.
CAT: BRP-00827
Molecular Formula: C31H40N3O3P
Molecular Weight: 533.65
Purity: >95%
Appearance: Light-yellow oily matter
Size Price Stock Quantity
-- -- --
Inquiry   
Storage: Store at -20 °C
InChIKey: TVYYYWLTEUUCSU-UHFFFAOYSA-N
Solubility: Soluble in Acetonitrile, DMF
CanonicalSMILES: CC(C)N(C(C)C)P(OCCC#N)OCCNC(C1=CC=CC=C1)(C2=CC=CC=C2)C3=CC=C(C=C3)OC
IUPAC Name: 3-[[di(propan-2-yl)amino]-[2-[[(4-methoxyphenyl)-diphenylmethyl]amino]ethoxy]phosphanyl]oxypropanenitrile
InChI: InChI=1S/C31H40N3O3P/c1-25(2)34(26(3)4)38(36-23-12-21-32)37-24-22-33-31(27-13-8-6-9-14-27,28-15-10-7-11-16-28)29-17-19-30(35-5)20-18-29/h6-11,13-20,25-26,33H,12,22-24H2,1-5H3
Synonyms: 2-cyanoethyl (2-(((4-methoxyphenyl)diphenylmethyl)amino)ethyl) diisopropylphosphoramidite; MMTr C2 linker Phosphoramidite; MMT-ethylamine-linker Phosphoramidite; NHMMTr-C2 Phosphoramidite

2'-OTBS U OMe-amidite

Description: 2'-OTBS U OMe-amidite is a reagent used for synthesizing modified oligonucleotides. It has uridine with a 2'-tert-butyldimethylsilyl (TBDMS) protecting group, which enhances stability during the synthesis process. This modification improves the stability and resistance of the oligonucleotides to degradation.
CAT: BRP-00828
CAS: 114207-67-9
Molecular Formula: C43H60N3O9PSi
Molecular Weight: 822.03
Purity: >95%
Appearance: White, off-white to faint yellow powder
Size Price Stock Quantity
-- -- --
Inquiry   
Storage: Store at -20 °C
InChIKey: AJKMTCZXJSDRLN-CYSIDSPMSA-N
Solubility: Soluble in Acetonitrile, DMF
CanonicalSMILES: CC(C)N(C(C)C)P(OC)OC1C(OC(C1O[Si](C)(C)C(C)(C)C)N2C=CC(=O)NC2=O)COC(C3=CC=CC=C3)(C4=CC=C(C=C4)OC)C5=CC=C(C=C5)OC
IUPAC Name: 1-[(2R,3R,4R,5R)-5-[[bis(4-methoxyphenyl)-phenylmethoxy]methyl]-3-[tert-butyl(dimethyl)silyl]oxy-4-[[di(propan-2-yl)amino]-methoxyphosphanyl]oxyoxolan-2-yl]pyrimidine-2,4-dione
InChI: InChI=1S/C43H60N3O9PSi/c1-29(2)46(30(3)4)56(51-10)54-38-36(53-40(45-27-26-37(47)44-41(45)48)39(38)55-57(11,12)42(5,6)7)28-52-43(31-16-14-13-15-17-31,32-18-22-34(49-8)23-19-32)33-20-24-35(50-9)25-21-33/h13-27,29-30,36,38-40H,28H2,1-12H3,(H,44,47,48)/t36-,38-,39-,40-,56?/m1/s1
Synonyms: (2R,3R,4R,5R)-2-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-4-((tert-butyldimethylsilyl)oxy)-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)tetrahydrofuran-3-yl methyl diisopropylphosphoramidite; 5'-O-DMTr-2'-O-TBDMS-U-3'-Methoxy-phosphoramidite; 5'-O-(4,4'-dimethoxytrityl)-2'-O-(t-butyl-dimethylsilyl)-uridine-3'-Methoxy-phosphoramidite; 2'-tBDSilyl Uridine methyl phosphoramidite

2'-OTBS C(Ac) OMe-amidite

Description: 2'-OTBS C(Ac) OMe-amidite is a modified phosphoramidite used in oligonucleotide synthesis to introduce 2'-OTBS modifications into RNA sequences, specifically targeting cytidine (C). It enhances the stability and specificity of RNA molecules and is commonly used in applications such as RNA interference, antisense therapy, and RNA structural studies.
CAT: BRP-00830
CAS: 1360559-84-7
Molecular Formula: C45H63N4O9PSi
Molecular Weight: 863.08
Purity: >95%
Appearance: White, off-white to faint yellow powder
Size Price Stock Quantity
-- -- --
Inquiry   
Storage: Store at -20 °C
InChIKey: TZHWOKHEMQAVPY-ZMHKPELYSA-N
Solubility: Soluble in Acetonitrile, DMF
CanonicalSMILES: O=C1N=C(C=CN1C2OC(COC(C=3C=CC=CC3)(C4=CC=C(OC)C=C4)C5=CC=C(OC)C=C5)C(OP(OC)N(C(C)C)C(C)C)C2O[Si](C)(C)C(C)(C)C)NC(=O)C
IUPAC Name: (2R,3R,4R,5R)-5-(4-acetamido-2-oxopyrimidin-1(2H)-yl)-2-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-4-((tert-butyldimethylsilyl)oxy)tetrahydrofuran-3-yl methyl diisopropylphosphoramidite
InChI: InChI=1S/C45H63N4O9PSi/c1-30(2)49(31(3)4)59(54-11)57-40-38(56-42(41(40)58-60(12,13)44(6,7)8)48-28-27-39(46-32(5)50)47-43(48)51)29-55-45(33-17-15-14-16-18-33,34-19-23-36(52-9)24-20-34)35-21-25-37(53-10)26-22-35/h14-28,30-31,38,40-42H,29H2,1-13H3,(H,46,47,50,51)/t38-,40-,41-,42-,59?/m1/s1
Synonyms: Cytidine, N-acetyl-5'-O-[bis(4-methoxyphenyl)phenylmethyl]-2'-O-[(1,1-dimethylethyl)dimethylsilyl]-, 3'-[methyl N,N-bis(1-methylethyl)phosphoramidite]; 5'-O-DMTr-2'-O-TBDMS-C(Ac)-3'-Methoxy-phosphoramidite; N4-acetyl-5'-O-(4,4'-dimethoxytrityl)-2'-O-(t-butyl-dimethylsilyl)-cytidine-3'-Methoxy-phosphoramidite

2'-OTBS A(Bz) OMe-amidite

Description: 2'-OTBS A(Bz) OMe-amidite is a reagent for oligonucleotide synthesis. It features adenosine with a tert-butyldimethylsilyl (TBDMS) group at the 2'-position and a benzoyl (bz) group protecting the amino group. This compound is used to incorporate modified adenosine into synthetic oligonucleotides, enhancing their stability and resistance to degradation.
CAT: BRP-00831
CAS: 118684-39-2
Molecular Formula: C51H65N6O8PSi
Molecular Weight: 949.18
Purity: >95%
Appearance: White, off-white to faint yellow powder
Size Price Stock Quantity
-- -- --
Inquiry   
Storage: Store at -20 °C
InChIKey: QECBNEWCSSUUAS-XOMUZYEBSA-N
Solubility: Soluble in Acetonitrile, DMF
CanonicalSMILES: O=C(NC1=NC=NC2=C1N=CN2C3OC(COC(C=4C=CC=CC4)(C5=CC=C(OC)C=C5)C6=CC=C(OC)C=C6)C(OP(OC)N(C(C)C)C(C)C)C3O[Si](C)(C)C(C)(C)C)C=7C=CC=CC7
IUPAC Name: (2R,3R,4R,5R)-5-(6-benzamido-9H-purin-9-yl)-2-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-4-((tert-butyldimethylsilyl)oxy)tetrahydrofuran-3-yl methyl diisopropylphosphoramidite
InChI: InChI=1S/C51H65N6O8PSi/c1-34(2)57(35(3)4)66(61-10)64-44-42(31-62-51(37-21-17-14-18-22-37,38-23-27-40(59-8)28-24-38)39-25-29-41(60-9)30-26-39)63-49(45(44)65-67(11,12)50(5,6)7)56-33-54-43-46(52-32-53-47(43)56)55-48(58)36-19-15-13-16-20-36/h13-30,32-35,42,44-45,49H,31H2,1-12H3,(H,52,53,55,58)/t42-,44-,45-,49-,66?/m1/s1
Synonyms: 5'-O-DMTr-2'-O-TBDMS-A(Bz)-3'-Methoxy-phosphoramidite; 2'-tBDSilyl Adenosine (n-bz) methyl phosphoramidite

Frequently Asked Questions (FAQ)

What are phosphoramidites used for?

Phosphoramidites are activated monomers used in solid-phase DNA and RNA oligonucleotide synthesis.

What is the difference between DNA and RNA phosphoramidites?

RNA phosphoramidites include additional 2′-hydroxyl protecting groups, making them more sensitive to moisture and handling conditions.

Why is moisture control important for phosphoramidites?

Moisture can cause premature hydrolysis of phosphoramidites, reducing coupling efficiency and synthesis yield.

Can phosphoramidites be used for long oligonucleotide synthesis?

Yes, high-quality phosphoramidites are essential for achieving good yields in long and complex oligonucleotide sequences.

Are modified phosphoramidites available for custom oligos?

Modified and specialty phosphoramidites are commonly used to introduce functional groups or labels into oligonucleotides.

* Only for research. Not suitable for any diagnostic or therapeutic use.

Our Products

MicroRNA Products

MicroRNA Products

MicroRNA (miRNA) is a class of small, naturally occurring non-coding RNA molecules that have important roles in the regulation of life activities and disease genesis.
siRNA Products

siRNA Products

Small interfering RNA (siRNA) is a stretch of RNA double-stranded between 20-25 nucleotides in length and is an important molecule in the RNAi process.
RNA Synthesis Reagents

RNA Synthesis Reagents

BOC RNA offers high quality cap analogs, CPGs for oligo synthesis, nucleosides, nucleotides, and phosphoramidites for RNA synthesis.
Liposome Products

Liposome Products

BOC RNA is dedicated to assisting you in exploring the complexity of liposomes, nucleic acid delivery mechanisms, and applications through our cutting-edge liposome delivery services.
mRNA Products

mRNA Products

BOC RNA provides finished RNAs for you to choose from, supporting RNA-related research and drug development.
Online Inquiry
Verification code

logo

Global Supplier of High-Quality RNA / DNA Products & Services.

facebook     twitter     linkedIn Ordering
Copyright © 2026 BOC Sciences. All rights reserved.
USA
    • International:
    • US & Canada (Toll free):
  • Fax:
  • Email:
UK
  • Tel:
Germany
Inquiry Basket
Loading ......
Delete selected Go to checkout