Phosphoramidites

Bis(5'-O-DMTr-2'-O-MOE-rG(iBu)-3'-oxy)-diisopropylphosphoramidite

Description: Bis(5'-O-DMTr-2'-O-MOE-rG(iBu)-3'-oxy)-diisopropylphosphoramidite comprises two molecules of 5'-O-DMTr-2'-O-MOE-rG(iBu)-3'-oxy linked by a diisopropylphosphoramidite group. Each 5'-O-DMTr-2'-O-MOE-rG(iBu)-3'-oxy unit is equipped with a diisopropylphosphoramidite group, facilitating its integration into oligonucleotide synthesis. It is utilized to introduce modified guanosine (rG) residues into RNA sequences, enhancing stability and target specificity.

CAT: BRP-00613

Molecular Formula: C82H98N11O18P

Molecular Weight: 1556.72

Purity: ≥92%

Size	Price	Stock	Quantity
--	--	--

Inquiry

Storage: Store at -20 °C

InChIKey: BXMZUGBTEMISAL-APUMCEBKSA-N

IUPAC Name: bis((2R,3R,4R,5R)-2-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-5-(2-isobutyramido-6-oxo-1,6-dihydro-9H-purin-9-yl)-4-(2-methoxyethoxy)tetrahydrofuran-3-yl) diisopropylphosphoramidite

InChI: InChI=1S/C82H98N11O18P/c1-49(2)73(94)87-79-85-71-65(75(96)89-79)83-47-91(71)77-69(104-43-41-98-9)67(63(108-77)45-106-81(53-21-17-15-18-22-53,55-25-33-59(100-11)34-26-55)56-27-35-60(101-12)36-28-56)110-112(93(51(5)6)52(7)8)111-68-64(109-78(70(68)105-44-42-99-10)92-48-84-66-72(92)86-80(90-76(66)97)88-74(95)50(3)4)46-107-82(54-23-19-16-20-24-54,57-29-37-61(102-13)38-30-57)58-31-39-62(103-14)40-32-58/h15-40,47-52,63-64,67-70,77-78H,41-46H2,1-14H3,(H2,85,87,89,94,96)(H2,86,88,90,95,97)/t63-,64-,67-,68-,69-,70-,77-,78-/m1/s1

Bis(5'-O-DMTr-2'-O-MOE-rA(Bz)-3'-oxy)-diisopropylphosphoramidite

Description: Bis(5'-O-DMTr-2'-O-MOE-rA(Bz)-3'-oxy)-diisopropylphosphoramidite consists of two molecules of 5'-O-DMTr-2'-O-MOE-rA(Bz)-3'-oxy linked by a diisopropylphosphoramidite group. Each 5'-O-DMTr-2'-O-MOE-rA(Bz)-3'-oxy unit is equipped with a diisopropylphosphoramidite group, facilitating its integration into oligonucleotide synthesis. It is used to introduce modified adenosine (rA) residues into RNA sequences, enhancing stability and target specificity.

CAT: BRP-00614

Molecular Formula: C88H94N11O16P

Molecular Weight: 1592.75

Purity: ≥92%

Size	Price	Stock	Quantity
--	--	--

Inquiry

Storage: Store at -20 °C

InChIKey: SSMWHJUZANQYIO-BDXQTOLXSA-N

IUPAC Name: bis((2R,3R,4R,5R)-5-(6-benzamido-9H-purin-9-yl)-2-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-4-(2-methoxyethoxy)tetrahydrofuran-3-yl) diisopropylphosphoramidite

InChI: InChI=1S/C88H94N11O16P/c1-57(2)99(58(3)4)116(114-75-71(51-110-87(61-27-19-13-20-28-61,63-31-39-67(104-7)40-32-63)64-33-41-68(105-8)42-34-64)112-85(77(75)108-49-47-102-5)97-55-93-73-79(89-53-91-81(73)97)95-83(100)59-23-15-11-16-24-59)115-76-72(52-111-88(62-29-21-14-22-30-62,65-35-43-69(106-9)44-36-65)66-37-45-70(107-10)46-38-66)113-86(78(76)109-50-48-103-6)98-56-94-74-80(90-54-92-82(74)98)96-84(101)60-25-17-12-18-26-60/h11-46,53-58,71-72,75-78,85-86H,47-52H2,1-10H3,(H,89,91,95,100)(H,90,92,96,101)/t71-,72-,75-,76-,77-,78-,85-,86-/m1/s1

DMTr-2'-O-EOE-rA(Bz)-3'-CE-Phosphoramidite

Description: DMTr-2'-O-EOE-rA(Bz)-3'-CE-Phosphoramidite is used in oligonucleotide synthesis and contains a 2'-O-ethoxyethyl (EOE) group at the 2'-position of adenosine (rA), along with benzoyl (Bz) protection on the adenine amino group. Additionally, it features a cyanoethyl (CE) group at the 3'-end to facilitate efficient coupling reactions during solid-phase synthesis. It is employed to introduce modified adenosine residues into RNA sequences, enhancing stability and target specificity.

CAT: BRP-00615

Molecular Formula: C51H60N7O9P

Molecular Weight: 946.05

Purity: ≥95%

Size	Price	Stock	Quantity
--	--	--

Inquiry

Storage: Store at -20 °C

InChIKey: FXYAXMLJVORSBX-SXQANJJUSA-N

CanonicalSMILES: CCOCCOC1C(C(OC1N2C=NC3=C(N=CN=C32)NC(=O)C4=CC=CC=C4)COC(C5=CC=CC=C5)(C6=CC=C(C=C6)OC)C7=CC=C(C=C7)OC)OP(N(C(C)C)C(C)C)OCCC#N

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-(2-ethoxyethoxy)oxolan-2-yl]purin-6-yl]benzamide

InChI: InChI=1S/C51H60N7O9P/c1-8-62-30-31-63-46-45(67-68(65-29-15-28-52)58(35(2)3)36(4)5)43(66-50(46)57-34-55-44-47(53-33-54-48(44)57)56-49(59)37-16-11-9-12-17-37)32-64-51(38-18-13-10-14-19-38,39-20-24-41(60-6)25-21-39)40-22-26-42(61-7)27-23-40/h9-14,16-27,33-36,43,45-46,50H,8,15,29-32H2,1-7H3,(H,53,54,56,59)/t43-,45-,46-,50-,68?/m1/s1

Synonyms: (2R,3R,4R,5R)-5-(6-Benzamido-9H-purin-9-yl)-2-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-4-(2-ethoxyethoxy)tetrahydrofuran-3-yl (2-cyanoethyl) diisopropylphosphoramidite

DMTr-2'-O-EOE-rG(iBu)-3'-CE-Phosphoramidite

Description: DMTr-2'-O-EOE-rG(iBu)-3'-CE-Phosphoramidite, utilized in oligonucleotide synthesis, features a 2'-O-ethoxyethyl (EOE) group at the 2'-position of guanosine (rG), with isobutyryl (iBu) protection on the guanine amino group. It also contains a cyanoethyl (CE) group at the 3'-end to facilitate efficient coupling reactions during solid-phase synthesis. It is employed to introduce modified guanosine residues into RNA sequences, enhancing stability and target specificity.

CAT: BRP-00616

CAS: 2253990-02-0

Molecular Formula: C48H62N7O10P

Molecular Weight: 928.04

Purity: ≥95%

Size	Price	Stock	Quantity
--	--	--

Inquiry

Storage: Store at -20 °C

InChIKey: FIYLELGPQAAWKS-USWYRWCRSA-N

CanonicalSMILES: N#CCCOP(OC1C(OC(N2C=NC=3C(=O)N=C(NC(=O)C(C)C)NC32)C1OCCOCC)COC(C=4C=CC=CC4)(C5=CC=C(OC)C=C5)C6=CC=C(OC)C=C6)N(C(C)C)C(C)C

IUPAC Name: (2R,3R,4R,5R)-2-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-4-(2-ethoxyethoxy)-5-(2-isobutyramido-6-oxo-1,6-dihydro-9H-purin-9-yl)tetrahydrofuran-3-yl (2-cyanoethyl) diisopropylphosphoramidite

InChI: InChI=1S/C48H62N7O10P/c1-10-60-27-28-61-42-41(65-66(63-26-14-25-49)55(32(4)5)33(6)7)39(64-46(42)54-30-50-40-43(54)51-47(53-45(40)57)52-44(56)31(2)3)29-62-48(34-15-12-11-13-16-34,35-17-21-37(58-8)22-18-35)36-19-23-38(59-9)24-20-36/h11-13,15-24,30-33,39,41-42,46H,10,14,26-29H2,1-9H3,(H2,51,52,53,56,57)/t39-,41-,42-,46-,66?/m1/s1

DMTr-2'-O-EOE-5-Me-rC(Bz)-3'-CE-Phosphoramidite

Description: DMTr-2'-O-EOE-5-Me-rC(Bz)-3'-CE-Phosphoramidite is utilized in oligonucleotide synthesis and contains a 2'-O-ethoxyethyl (EOE) group at the 2'-position of 5-methylcytidine (5-Me-rC), along with benzoyl (Bz) protection on the cytosine amino group. Additionally, it features a cyanoethyl (CE) group at the 3'-end to facilitate efficient coupling reactions during solid-phase synthesis. It is employed to introduce modified 5-methylcytidine residues into RNA sequences, enhancing stability and target specificity.

CAT: BRP-00617

Molecular Formula: C51H62N5O10P

Molecular Weight: 936.06

Purity: ≥95%

Size	Price	Stock	Quantity
--	--	--

Inquiry

Storage: Store at -20 °C

InChIKey: GFURHQMVDLZCAG-JMTVAXSASA-N

IUPAC Name: (2R,3R,4R,5R)-5-(4-benzamido-5-methyl-2-oxopyrimidin-1(2H)-yl)-2-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-4-(2-ethoxyethoxy)tetrahydrofuran-3-yl (2-cyanoethyl) diisopropylphosphoramidite

InChI: InChI=1S/C51H62N5O10P/c1-9-61-31-32-62-46-45(66-67(64-30-16-29-52)56(35(2)3)36(4)5)44(65-49(46)55-33-37(6)47(54-50(55)58)53-48(57)38-17-12-10-13-18-38)34-63-51(39-19-14-11-15-20-39,40-21-25-42(59-7)26-22-40)41-23-27-43(60-8)28-24-41/h10-15,17-28,33,35-36,44-46,49H,9,16,30-32,34H2,1-8H3,(H,53,54,57,58)/t44-,45-,46-,49-,67?/m1/s1

DMTr-3'-O-MOE-5-Me-rC(Bz)-2'-CE-Phosphoramidite

Description: DMTr-3'-O-MOE-5-Me-rC(Bz)-2'-CE-Phosphoramidite is used in oligonucleotide synthesis and contains a 3'-O-methoxyethyl (MOE) group at the 3'-position of 5-methylcytidine (5-Me-rC), with benzoyl (Bz) protection on the cytosine amino group. Additionally, it features a cyanoethyl (CE) group at the 2'-end to facilitate efficient coupling reactions during solid-phase synthesis. It is employed to introduce modified 5-methylcytidine residues into RNA sequences, enhancing stability and target specificity.

CAT: BRP-00618

CAS: 1098233-10-3

Molecular Formula: C50H60N5O10P

Molecular Weight: 922.03

Purity: ≥95%

Size	Price	Stock	Quantity
--	--	--

Inquiry

Storage: Store at -20 °C

InChIKey: GOMXXEFGGBGLGJ-GICDFOIUSA-N

CanonicalSMILES: CC1=CN(C(=O)N=C1NC(=O)C2=CC=CC=C2)C3C(C(C(O3)COC(C4=CC=CC=C4)(C5=CC=C(C=C5)OC)C6=CC=C(C=C6)OC)OCCOC)OP(N(C(C)C)C(C)C)OCCC#N

IUPAC Name: N-[1-[(2R,3R,4R,5R)-5-[[bis(4-methoxyphenyl)-phenylmethoxy]methyl]-3-[2-cyanoethoxy-[di(propan-2-yl)amino]phosphanyl]oxy-4-(2-methoxyethoxy)oxolan-2-yl]-5-methyl-2-oxopyrimidin-4-yl]benzamide

InChI: InChI=1S/C50H60N5O10P/c1-34(2)55(35(3)4)66(63-29-15-28-51)65-45-44(61-31-30-58-6)43(64-48(45)54-32-36(5)46(53-49(54)57)52-47(56)37-16-11-9-12-17-37)33-62-50(38-18-13-10-14-19-38,39-20-24-41(59-7)25-21-39)40-22-26-42(60-8)27-23-40/h9-14,16-27,32,34-35,43-45,48H,15,29-31,33H2,1-8H3,(H,52,53,56,57)/t43-,44-,45-,48-,66?/m1/s1

Synonyms: 3'-O-MOE-5Me-C(Bz)-2'-phosphoramidite; N4-Bz-5'-O-DMTr-3'-O-(2-methoxyethyl)-5-methyl cytidine-2'-CED-phosphoramidite; Cytidine, N-benzoyl-5'-O-[bis(4-methoxyphenyl)phenylmethyl]-3'-O-(2-methoxyethyl)-5-methyl-, 2'-[2-cyanoethyl N,N-bis(1-methylethyl)phosphoramidite]

DMTr-3'-O-MOE-rA(Bz)-2'-CE-Phosphoramidite

Description: DMTr-3'-O-MOE-rA(Bz)-2'-CE-Phosphoramidite, utilized in oligonucleotide synthesis, features a 3'-O-methoxyethyl (MOE) group at the 3'-position of adenosine (rA), with benzoyl (Bz) protection on the adenine amino group. It also contains a cyanoethyl (CE) group at the 2'-end to facilitate efficient coupling reactions during solid-phase synthesis. It is employed to introduce modified adenosine residues into RNA sequences, enhancing stability and target specificity.

CAT: BRP-00619

CAS: 256224-01-8

Molecular Formula: C50H58N7O9P

Molecular Weight: 932.03

Purity: ≥95%

Size	Price	Stock	Quantity
--	--	--

Inquiry

Storage: Store at -20 °C

InChIKey: FODCLDRFHMYZMX-HDMAWCRFSA-N

CanonicalSMILES: CC(C)N(C(C)C)P(OCCC#N)OC1C(C(OC1N2C=NC3=C(N=CN=C32)NC(=O)C4=CC=CC=C4)COC(C5=CC=CC=C5)(C6=CC=C(C=C6)OC)C7=CC=C(C=C7)OC)OCCOC

IUPAC Name: N-[9-[(2R,3R,4R,5R)-5-[[bis(4-methoxyphenyl)-phenylmethoxy]methyl]-3-[2-cyanoethoxy-[di(propan-2-yl)amino]phosphanyl]oxy-4-(2-methoxyethoxy)oxolan-2-yl]purin-6-yl]benzamide

InChI: InChI=1S/C50H58N7O9P/c1-34(2)57(35(3)4)67(64-28-14-27-51)66-45-44(62-30-29-59-5)42(65-49(45)56-33-54-43-46(52-32-53-47(43)56)55-48(58)36-15-10-8-11-16-36)31-63-50(37-17-12-9-13-18-37,38-19-23-40(60-6)24-20-38)39-21-25-41(61-7)26-22-39/h8-13,15-26,32-35,42,44-45,49H,14,28-31H2,1-7H3,(H,52,53,55,58)/t42-,44-,45-,49-,67?/m1/s1

Synonyms: 3'-O-MOE-A(Bz)-2'-CED-phosphoramidite; (2R,3R,4R,5R)-2-(6-Benzamido-9H-purin-9-yl)-5-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-4-(2-methoxyethoxy)tetrahydrofuran-3-yl (2-cyanoethyl) diisopropylphosphoramidite; Adenosine, N-benzoyl-5'-O-[bis(4-methoxyphenyl)phenylmethyl]-3'-O-(2-methoxyethyl)-, 2'-[2-cyanoethyl bis(1-methylethyl)phosphoramidite]; N6-Bz-5'-O-DMTr-3'-O-(2-methoxyethyl) adenosine-2'-CED-phosphoramidite

DMTr-3'-O-MOE-rG(iBu)-2'-CE-Phosphoramidite

Description: DMTr-3'-O-MOE-rG(iBu)-2'-CE-Phosphoramidite is utilized in oligonucleotide synthesis and contains a 3'-O-methoxyethyl (MOE) group at the 3'-position of guanosine (rG), with isobutyryl (iBu) protection on the guanine amino group. Additionally, it features a cyanoethyl (CE) group at the 2'-end to facilitate efficient coupling reactions during solid-phase synthesis. It is employed to introduce modified guanosine residues into RNA sequences, enhancing stability and target specificity.

CAT: BRP-00620

CAS: 256224-06-3

Molecular Formula: C47H60N7O10P

Molecular Weight: 914.01

Purity: ≥95%

Appearance: White to off-white foam solid

Size	Price	Stock	Quantity
--	--	--

Inquiry

Storage: Store at -20 °C, under inert atmosphere

InChIKey: BWLKVJLYUDLOLH-SBCRAQIVSA-N

Solubility: Soluble in Acetone, Chloroform, DMSO, Ethanol, Methanol

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)OCCOC)OP(N(C(C)C)C(C)C)OCCC#N

IUPAC Name: N-[9-[(2R,3R,4R,5R)-5-[[bis(4-methoxyphenyl)-phenylmethoxy]methyl]-3-[2-cyanoethoxy-[di(propan-2-yl)amino]phosphanyl]oxy-4-(2-methoxyethoxy)oxolan-2-yl]-6-oxo-1H-purin-2-yl]-2-methylpropanamide

InChI: InChI=1S/C47H60N7O10P/c1-30(2)43(55)51-46-50-42-39(44(56)52-46)49-29-53(42)45-41(64-65(62-25-13-24-48)54(31(3)4)32(5)6)40(60-27-26-57-7)38(63-45)28-61-47(33-14-11-10-12-15-33,34-16-20-36(58-8)21-17-34)35-18-22-37(59-9)23-19-35/h10-12,14-23,29-32,38,40-41,45H,13,25-28H2,1-9H3,(H2,50,51,52,55,56)/t38-,40-,41-,45-,65?/m1/s1

Synonyms: 3'-O-MOE-G(iBu)-2'-phosphoramidite; 5'-O-DMTr-N2-iso-butyroyl-3'-O-(2-methoxyethyl)guanosine-2'-CED-phosphoramidite; Guanosine, 5'-O-[bis(4-methoxyphenyl)phenylmethyl]-3'-O-(2-methoxyethyl)-N-(2-methyl-1-oxopropyl)-, 2'-[2-cyanoethyl bis(1-methylethyl)phosphoramidite]; 5'-O-(4,4'-Dimethoxytrityl)-N2-iso-butyroyl-3'-O-(2-methoxyethyl)guanosine-2'-O-[(2-cyanoethyl)(N,N-diisopropyl)]phosphoramidite

DMTr-2'-O-MOEOE-5-Me-rC(Bz)-3'-CE-Phosphoramidite

Description: DMTr-2'-O-MOEOE-5-Me-rC(Bz)-3'-CE-Phosphoramidite, employed in oligonucleotide synthesis, features a methoxyethoxy (MOEOE) group at the 2'-O position and a benzoyl (Bz) protecting group on the 5-methylcytosine (5-Me-rC) amino group. The 3'-end is functionalized with a cyanoethyl (CE) group, facilitating efficient coupling reactions during solid-phase synthesis. It is utilized to introduce modified cytosine residues into nucleic acid sequences, enhancing stability and target specificity for various research applications, including RNA labeling, probing, and therapeutic development.

CAT: BRP-00621

Molecular Formula: C52H64N5O11P

Molecular Weight: 966.08

Purity: ≥95%

Size	Price	Stock	Quantity
--	--	--

Inquiry

Storage: Store at -20 °C

InChIKey: FKWHQFYMJVJQSH-ACHZJAKQSA-N

IUPAC Name: (2R,3R,4R,5R)-5-(4-benzamido-5-methyl-2-oxopyrimidin-1(2H)-yl)-2-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-4-(2-(2-methoxyethoxy)ethoxy)tetrahydrofuran-3-yl (2-cyanoethyl) diisopropylphosphoramidite

InChI: InChI=1S/C52H64N5O11P/c1-36(2)57(37(3)4)69(66-29-15-28-53)68-46-45(35-65-52(40-18-13-10-14-19-40,41-20-24-43(61-7)25-21-41)42-22-26-44(62-8)27-23-42)67-50(47(46)64-33-32-63-31-30-60-6)56-34-38(5)48(55-51(56)59)54-49(58)39-16-11-9-12-17-39/h9-14,16-27,34,36-37,45-47,50H,15,29-33,35H2,1-8H3,(H,54,55,58,59)/t45-,46-,47-,50-,69?/m1/s1

Synonyms: 2'-MOEOE 5-Me-rC(Bz) amidite

DMTr-2'-O-MOEOE-rG(iBu)-3'-CE-Phosphoramidite

Description: DMTr-2'-O-MOEOE-rG(iBu)-3'-CE-Phosphoramidite, utilized in oligonucleotide synthesis, contains a methoxyethoxy (MOEOE) group at the 2'-O position and an isobutyryl (iBu) protecting group on the guanine amino group. The 3'-end is functionalized with a cyanoethyl (CE) group, facilitating efficient coupling reactions during solid-phase synthesis. It is employed to introduce modified guanine residues into nucleic acid sequences, enhancing stability and target specificity for applications such as RNA research, gene silencing, and aptamer development.

CAT: BRP-00622

Molecular Formula: C49H64N7O11P

Molecular Weight: 958.06

Purity: ≥95%

Appearance: White, off-white to faint yellow powder

Size	Price	Stock	Quantity
--	--	--

Inquiry

Storage: Store at -20 °C

InChIKey: OATUMETWWCLSRW-LCVXBTAASA-N

IUPAC Name: (2R,3R,4R,5R)-2-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-5-(2-isobutyramido-6-oxo-1,6-dihydro-9H-purin-9-yl)-4-(2-(2-methoxyethoxy)ethoxy)tetrahydrofuran-3-yl (2-cyanoethyl) diisopropylphosphoramidite

InChI: InChI=1S/C49H64N7O11P/c1-32(2)45(57)53-48-52-44-41(46(58)54-48)51-31-55(44)47-43(63-29-28-62-27-26-59-7)42(67-68(65-25-13-24-50)56(33(3)4)34(5)6)40(66-47)30-64-49(35-14-11-10-12-15-35,36-16-20-38(60-8)21-17-36)37-18-22-39(61-9)23-19-37/h10-12,14-23,31-34,40,42-43,47H,13,25-30H2,1-9H3,(H2,52,53,54,57,58)/t40-,42-,43-,47-,68?/m1/s1

Synonyms: 2'-MOEOE rG(iBu) amidite; N2-iBu-DMT-2'-O-MOEOE-Gr-CE-Phosphoramidite; N2-isobutyryl-5'-O-(4,4'-dimethoxytrityl)-2'-O-(2-(2-Methoxyethoxy)ethyl)-guanosine-3'-cyanoethyl Phosphoramidite

DMTr-2'-O-MOEOE-rA(Bz)-3'-CE-Phosphoramidite

Description: DMTr-2'-O-MOEOE-rA(Bz)-3'-CE-Phosphoramidite is utilized in oligonucleotide synthesis, featuring a methoxyethoxy (MOEOE) group at the 2'-O position and a benzoyl (Bz) protecting group on the adenine amino group. The 3'-end is functionalized with a cyanoethyl (CE) group, facilitating efficient coupling reactions during solid-phase synthesis. It is employed to introduce modified adenine residues into nucleic acid sequences, enhancing stability and target specificity for various molecular biology applications, including RNA labeling, structural studies, and gene regulation research.

CAT: BRP-00623

Molecular Formula: C52H62N7O10P

Molecular Weight: 976.08

Purity: ≥95%

Appearance: Off-white solid

Size	Price	Stock	Quantity
--	--	--

Inquiry

Storage: Store at -20 °C

InChIKey: PKYUXPBRGLVQBQ-MABFDDSHSA-N

Solubility: Soluble in Acetonitrile, DMF

CanonicalSMILES: CC(C)N(C(C)C)P(OCCC#N)OC1C(OC(C1OCCOCCOC)N2C=NC3=C(N=CN=C32)NC(=O)C4=CC=CC=C4)COC(C5=CC=CC=C5)(C6=CC=C(C=C6)OC)C7=CC=C(C=C7)OC

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-[2-(2-methoxyethoxy)ethoxy]oxolan-2-yl]purin-6-yl]benzamide

InChI: InChI=1S/C52H62N7O10P/c1-36(2)59(37(3)4)70(67-28-14-27-53)69-46-44(33-66-52(39-17-12-9-13-18-39,40-19-23-42(62-6)24-20-40)41-21-25-43(63-7)26-22-41)68-51(47(46)65-32-31-64-30-29-61-5)58-35-56-45-48(54-34-55-49(45)58)57-50(60)38-15-10-8-11-16-38/h8-13,15-26,34-37,44,46-47,51H,14,28-33H2,1-7H3,(H,54,55,57,60)/t44-,46-,47-,51-,70?/m1/s1

Synonyms: (2R,3R,4R,5R)-5-(6-Benzamido-9H-purin-9-yl)-2-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-4-(2-(2-methoxyethoxy)ethoxy)tetrahydrofuran-3-yl (2-cyanoethyl) diisopropylphosphoramidite; 2'-MOEOE A(Bz) amidite; N6-Bz-DMT-2'-O-MOEOE-Ar-CE-Phosphoramidite; N6-benzoyl-5'-O-(4,4'-dimethoxytrityl)-2'-O-(2-(2-Methoxyethoxy)ethyl)-adenosine-3'-cyanoethyl Phosphoramidite

DMTr-2'-O-Bu-rA(Bz)-3'-CE-Phosphoramidite

Description: DMTr-2'-O-Bu-rA(Bz)-3'-CE-Phosphoramidite, used in oligonucleotide synthesis, features a butyl (Bu) group at the 2'-O position, and a benzoyl (Bz) protecting group on the adenine amino group. The 3'-end is functionalized with a cyanoethyl (CE) group, facilitating efficient coupling reactions during solid-phase synthesis. It is employed to introduce modified adenine residues into nucleic acid sequences, enhancing stability and target specificity for applications such as RNA labeling, structural studies, and gene regulation research.

CAT: BRP-00624

Molecular Formula: C51H60N7O8P

Molecular Weight: 930.06

Purity: ≥95%

Size	Price	Stock	Quantity
--	--	--

Inquiry

Storage: Store at -20 °C

InChIKey: PGNPDHTYAGNPAM-LTMMGAFGSA-N

CanonicalSMILES: CCCCOC1C(C(OC1N2C=NC3=C(N=CN=C32)NC(=O)C4=CC=CC=C4)COC(C5=CC=CC=C5)(C6=CC=C(C=C6)OC)C7=CC=C(C=C7)OC)OP(N(C(C)C)C(C)C)OCCC#N

IUPAC Name: N-[9-[(2R,3R,4R,5R)-5-[[bis(4-methoxyphenyl)-phenylmethoxy]methyl]-3-butoxy-4-[2-cyanoethoxy-[di(propan-2-yl)amino]phosphanyl]oxyoxolan-2-yl]purin-6-yl]benzamide

InChI: InChI=1S/C51H60N7O8P/c1-8-9-30-62-46-45(66-67(64-31-16-29-52)58(35(2)3)36(4)5)43(65-50(46)57-34-55-44-47(53-33-54-48(44)57)56-49(59)37-17-12-10-13-18-37)32-63-51(38-19-14-11-15-20-38,39-21-25-41(60-6)26-22-39)40-23-27-42(61-7)28-24-40/h10-15,17-28,33-36,43,45-46,50H,8-9,16,30-32H2,1-7H3,(H,53,54,56,59)/t43-,45-,46-,50-,67?/m1/s1

Synonyms: (2R,3R,4R,5R)-5-(6-Benzamido-9H-purin-9-yl)-2-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-4-butoxytetrahydrofuran-3-yl (2-cyanoethyl) diisopropylphosphoramidite

DMTr-2'-O-Et-rA(Bz)-3'-CE-Phosphoramidite

Description: DMTr-2'-O-Et-rA(Bz)-3'-CE-Phosphoramidite, utilized in oligonucleotide synthesis, contains an ethyl (Et) group at the 2'-O position, and a benzoyl (Bz) protecting group on the adenine amino group. The 3'-end is functionalized with a cyanoethyl (CE) group, facilitating efficient coupling reactions during solid-phase synthesis. It is employed to introduce modified adenine residues into nucleic acid sequences, enhancing stability and target specificity for various molecular biology applications, including RNA labeling, gene synthesis, and RNA interference studies.

CAT: BRP-00625

Molecular Formula: C49H56N7O8P

Molecular Weight: 902.00

Purity: ≥95%

Size	Price	Stock	Quantity
--	--	--

Inquiry

Storage: Store at -20 °C

InChIKey: BWEYMSXPRQAMFY-FVPMUMJWSA-N

CanonicalSMILES: CCOC1C(C(OC1N2C=NC3=C(N=CN=C32)NC(=O)C4=CC=CC=C4)COC(C5=CC=CC=C5)(C6=CC=C(C=C6)OC)C7=CC=C(C=C7)OC)OP(N(C(C)C)C(C)C)OCCC#N

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-ethoxyoxolan-2-yl]purin-6-yl]benzamide

InChI: InChI=1S/C49H56N7O8P/c1-8-60-44-43(64-65(62-29-15-28-50)56(33(2)3)34(4)5)41(63-48(44)55-32-53-42-45(51-31-52-46(42)55)54-47(57)35-16-11-9-12-17-35)30-61-49(36-18-13-10-14-19-36,37-20-24-39(58-6)25-21-37)38-22-26-40(59-7)27-23-38/h9-14,16-27,31-34,41,43-44,48H,8,15,29-30H2,1-7H3,(H,51,52,54,57)/t41-,43-,44-,48-,65?/m1/s1

Synonyms: (2R,3R,4R,5R)-5-(6-Benzamido-9H-purin-9-yl)-2-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-4-ethoxytetrahydrofuran-3-yl (2-cyanoethyl) diisopropylphosphoramidite

DMTr-2'-O-Bu-5-Me-rC(Bz)-3'-CE-Phosphoramidite

Description: DMTr-2'-O-Bu-5-Me-rC(Bz)-3'-CE-Phosphoramidite, utilized in oligonucleotide synthesis, features a butyl (Bu) group at the 2'-O position, and a benzoyl (Bz) protecting group on the 5-methylcytosine (5-Me-rC) amino group. The 3'-end is functionalized with a cyanoethyl (CE) group, facilitating efficient coupling reactions during solid-phase synthesis. It is employed to introduce modified cytosine residues into nucleic acid sequences, enhancing stability and target specificity for applications such as RNA labeling, probing, and therapeutic development.

CAT: BRP-00626

Molecular Formula: C51H62N5O9P

Molecular Weight: 920.06

Purity: ≥95%

Size	Price	Stock	Quantity
--	--	--

Inquiry

Storage: Store at -20 °C

InChIKey: JRVKTZYKHMIWMA-BZPNBFHRSA-N

IUPAC Name: (2R,3R,4R,5R)-5-(4-benzamido-5-methyl-2-oxopyrimidin-1(2H)-yl)-2-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-4-butoxytetrahydrofuran-3-yl (2-cyanoethyl) diisopropylphosphoramidite

InChI: InChI=1S/C51H62N5O9P/c1-9-10-31-61-46-45(65-66(63-32-17-30-52)56(35(2)3)36(4)5)44(64-49(46)55-33-37(6)47(54-50(55)58)53-48(57)38-18-13-11-14-19-38)34-62-51(39-20-15-12-16-21-39,40-22-26-42(59-7)27-23-40)41-24-28-43(60-8)29-25-41/h11-16,18-29,33,35-36,44-46,49H,9-10,17,31-32,34H2,1-8H3,(H,53,54,57,58)/t44-,45-,46-,49-,66?/m1/s1

DMTr-2'-O-Et-5-Me-rC(Bz)-3'-CE-Phosphoramidite

Description: DMTr-2'-O-Et-5-Me-rC(Bz)-3'-CE-Phosphoramidite, utilized in oligonucleotide synthesis, features an ethyl (Et) group at the 2'-O position, and a benzoyl (Bz) protecting group on the 5-methylcytosine (5-Me-rC) amino group. The 3'-end is functionalized with a cyanoethyl (CE) group, facilitating efficient coupling reactions during solid-phase synthesis. It is employed to introduce modified cytosine residues into nucleic acid sequences, enhancing stability and target specificity for various research applications, including RNA labeling, probing, and therapeutic development.

CAT: BRP-00627

Molecular Formula: C49H58N5O9P

Molecular Weight: 892.00

Purity: ≥95%

Size	Price	Stock	Quantity
--	--	--

Inquiry

Storage: Store at -20 °C

InChIKey: NKWGOVVNANYUQH-ADJAFLDTSA-N

IUPAC Name: (2R,3R,4R,5R)-5-(4-benzamido-5-methyl-2-oxopyrimidin-1(2H)-yl)-2-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-4-ethoxytetrahydrofuran-3-yl (2-cyanoethyl) diisopropylphosphoramidite

InChI: InChI=1S/C49H58N5O9P/c1-9-59-44-43(63-64(61-30-16-29-50)54(33(2)3)34(4)5)42(62-47(44)53-31-35(6)45(52-48(53)56)51-46(55)36-17-12-10-13-18-36)32-60-49(37-19-14-11-15-20-37,38-21-25-40(57-7)26-22-38)39-23-27-41(58-8)28-24-39/h10-15,17-28,31,33-34,42-44,47H,9,16,30,32H2,1-8H3,(H,51,52,55,56)/t42-,43-,44-,47-,64?/m1/s1

DMTr-2'-O-Bu-rG(iBu)-3'-CE-Phosphoramidite

Description: DMTr-2'-O-Bu-rG(iBu)-3'-CE-Phosphoramidite is used in oligonucleotide synthesis, featuring a butyl (Bu) group at the 2'-O position, and an isobutyryl (iBu) protecting group on the guanine amino group. The 3'-end is functionalized with a cyanoethyl (CE) group, facilitating efficient coupling reactions during solid-phase synthesis. It is employed to introduce modified guanine residues into nucleic acid sequences, enhancing stability and target specificity for applications such as RNA labeling, probing, and therapeutic development.

CAT: BRP-00628

Molecular Formula: C48H62N7O9P

Molecular Weight: 912.04

Purity: ≥95%

Size	Price	Stock	Quantity
--	--	--

Inquiry

Storage: Store at -20 °C

InChIKey: BOYCEYCODXCBOY-VKFKYRIUSA-N

IUPAC Name: (2R,3R,4R,5R)-2-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-4-butoxy-5-(2-isobutyramido-6-oxo-1,6-dihydro-9H-purin-9-yl)tetrahydrofuran-3-yl (2-cyanoethyl) diisopropylphosphoramidite

InChI: InChI=1S/C48H62N7O9P/c1-10-11-27-60-42-41(64-65(62-28-15-26-49)55(32(4)5)33(6)7)39(63-46(42)54-30-50-40-43(54)51-47(53-45(40)57)52-44(56)31(2)3)29-61-48(34-16-13-12-14-17-34,35-18-22-37(58-8)23-19-35)36-20-24-38(59-9)25-21-36/h12-14,16-25,30-33,39,41-42,46H,10-11,15,27-29H2,1-9H3,(H2,51,52,53,56,57)/t39-,41-,42-,46-,65?/m1/s1

DMTr-2'-O-Et-rG(iBu)-3'-CE-Phosphoramidite

Description: DMTr-2'-O-Et-rG(iBu)-3'-CE-Phosphoramidite, utilized in oligonucleotide synthesis, contains an ethyl (Et) group at the 2'-O position, and an isobutyryl (iBu) protecting group on the guanine amino group. The 3'-end is functionalized with a cyanoethyl (CE) group, facilitating efficient coupling reactions during solid-phase synthesis. It is employed to introduce modified guanine residues into nucleic acid sequences, enhancing stability and target specificity for various molecular biology applications, including RNA labeling, probing, and therapeutic development.

CAT: BRP-00629

Molecular Formula: C46H58N7O9P

Molecular Weight: 883.98

Purity: ≥95%

Size	Price	Stock	Quantity
--	--	--

Inquiry

Storage: Store at -20 °C

InChIKey: VAXVPZPBYJLJJN-NOYBBXANSA-N

IUPAC Name: (2R,3R,4R,5R)-2-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-4-ethoxy-5-(2-isobutyramido-6-oxo-1,6-dihydro-9H-purin-9-yl)tetrahydrofuran-3-yl (2-cyanoethyl) diisopropylphosphoramidite

InChI: InChI=1S/C46H58N7O9P/c1-10-58-40-39(62-63(60-26-14-25-47)53(30(4)5)31(6)7)37(61-44(40)52-28-48-38-41(52)49-45(51-43(38)55)50-42(54)29(2)3)27-59-46(32-15-12-11-13-16-32,33-17-21-35(56-8)22-18-33)34-19-23-36(57-9)24-20-34/h11-13,15-24,28-31,37,39-40,44H,10,14,26-27H2,1-9H3,(H2,49,50,51,54,55)/t37-,39-,40-,44-,63?/m1/s1

DMTr-2'-O-(Methyl behenate)-rC(Ac)-3'-CE-Phosphoramidite

Description: DMTr-2'-O-(Methyl behenate)-rC(Ac)-3'-CE-Phosphoramidite, employed in oligonucleotide synthesis, features a methyl behenate group at the 2'-O position, and an acetyl (Ac) protecting group on the cytosine amino group. The 3'-end is functionalized with a cyanoethyl (CE) group, facilitating efficient coupling reactions during solid-phase synthesis. It is used to introduce modified cytosine residues into nucleic acid sequences, enhancing stability and target specificity for applications such as RNA labeling, structural studies, and gene regulation research.

CAT: BRP-00630

Molecular Formula: C64H94N5O11P

Molecular Weight: 1140.45

Purity: ≥95%

Size	Price	Stock	Quantity
--	--	--

Inquiry

Storage: Store at -20 °C

InChIKey: PKSNKLQRIFOCKB-QLODOALFSA-N

IUPAC Name: methyl 22-(((2R,3R,4R,5R)-2-(4-acetamido-2-oxopyrimidin-1(2H)-yl)-5-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-4-(((2-cyanoethoxy)(diisopropylamino)phosphaneyl)oxy)tetrahydrofuran-3-yl)oxy)docosanoate

InChI: InChI=1S/C64H94N5O11P/c1-49(2)69(50(3)4)81(78-47-31-44-65)80-60-57(48-77-64(52-32-27-26-28-33-52,53-35-39-55(73-6)40-36-53)54-37-41-56(74-7)42-38-54)79-62(68-45-43-58(66-51(5)70)67-63(68)72)61(60)76-46-30-25-23-21-19-17-15-13-11-9-10-12-14-16-18-20-22-24-29-34-59(71)75-8/h26-28,32-33,35-43,45,49-50,57,60-62H,9-25,29-31,34,46-48H2,1-8H3,(H,66,67,70,72)/t57-,60-,61-,62-,81?/m1/s1

DMTr-2'-O-C22-rU-3'-CE-Phosphoramidite

Description: DMTr-2'-O-C22-rU-3'-CE-Phosphoramidite, utilized in oligonucleotide synthesis, contains a C22 group at the 2'-O position, and a uracil (rU) nucleoside. The 3'-end is functionalized with a cyanoethyl (CE) group, facilitating efficient coupling reactions during solid-phase synthesis. It is employed to introduce modified uracil residues with extended carbon chains into nucleic acid sequences, enhancing stability and target specificity for various molecular biology applications, including RNA structural studies, aptamer development, and gene regulation research.

CAT: BRP-00631

CAS: 2923115-86-8

Molecular Formula: C61H91N4O9P

Molecular Weight: 1055.39

Purity: ≥95%

Size	Price	Stock	Quantity
--	--	--

Inquiry

Storage: Store at -20 °C

InChIKey: UVVBAOHROLTNIE-PGNDMMQRSA-N

CanonicalSMILES: CCCCCCCCCCCCCCCCCCCCCCOC1C(C(OC1N2C=CC(=O)NC2=O)COC(C3=CC=CC=C3)(C4=CC=C(C=C4)OC)C5=CC=C(C=C5)OC)OP(N(C(C)C)C(C)C)OCCC#N

IUPAC Name: 3-[[(2R,3R,4R,5R)-2-[[bis(4-methoxyphenyl)-phenylmethoxy]methyl]-5-(2,4-dioxopyrimidin-1-yl)-4-docosoxyoxolan-3-yl]oxy-[di(propan-2-yl)amino]phosphanyl]oxypropanenitrile

InChI: InChI=1S/C61H91N4O9P/c1-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-24-25-26-30-45-70-58-57(74-75(72-46-31-43-62)65(48(2)3)49(4)5)55(73-59(58)64-44-42-56(66)63-60(64)67)47-71-61(50-32-28-27-29-33-50,51-34-38-53(68-6)39-35-51)52-36-40-54(69-7)41-37-52/h27-29,32-42,44,48-49,55,57-59H,8-26,30-31,45-47H2,1-7H3,(H,63,66,67)/t55-,57-,58-,59-,75?/m1/s1

Synonyms: (2R,3R,4R,5R)-2-((Bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-4-(docosyloxy)tetrahydrofuran-3-yl (2-cyanoethyl) diisopropylphosphoramidite

DMTr-2'-O-C6-rU-3'-CE-Phosphoramidite

Description: DMTr-2'-O-C6-rU-3'-CE-Phosphoramidite is used in oligonucleotide synthesis and features a C6 group at the 2'-O position, and a uracil (rU) nucleoside. The 3'-end is functionalized with a cyanoethyl (CE) group, facilitating efficient coupling reactions during solid-phase synthesis. It is employed to introduce modified uracil residues with short carbon chains into nucleic acid sequences, enhancing stability and target specificity for applications such as RNA labeling, gene silencing, and aptamer development.

CAT: BRP-00632

CAS: 2382942-78-9

Molecular Formula: C45H59N4O9P

Molecular Weight: 830.96

Purity: ≥95%

Size	Price	Stock	Quantity
--	--	--

Inquiry

Storage: Store at -20 °C

InChIKey: WMIJYXRHECYAIW-ACVVKSTRSA-N

CanonicalSMILES: N#CCCOP(OC1C(OC(N2C=CC(=O)NC2=O)C1OCCCCCC)COC(C=3C=CC=CC3)(C4=CC=C(OC)C=C4)C5=CC=C(OC)C=C5)N(C(C)C)C(C)C

IUPAC Name: (2R,3R,4R,5R)-2-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-4-(hexyloxy)tetrahydrofuran-3-yl (2-cyanoethyl) diisopropylphosphoramidite

InChI: InChI=1S/C45H59N4O9P/c1-8-9-10-14-29-54-42-41(58-59(56-30-15-27-46)49(32(2)3)33(4)5)39(57-43(42)48-28-26-40(50)47-44(48)51)31-55-45(34-16-12-11-13-17-34,35-18-22-37(52-6)23-19-35)36-20-24-38(53-7)25-21-36/h11-13,16-26,28,32-33,39,41-43H,8-10,14-15,29-31H2,1-7H3,(H,47,50,51)/t39-,41-,42-,43-,59?/m1/s1

Synonyms: 2'-O-hexyl U amidite; Uridine, 5'-O-[bis(4-methoxyphenyl)phenylmethyl]-2'-O-hexyl-, 3'-[2-cyanoethyl N,N-bis(1-methylethyl)phosphoramidite]

Bis(5'-O-DMTr-2'-O-MOE-rG(iBu)-3'-oxy)-diisopropylphosphoramidite

Bis(5'-O-DMTr-2'-O-MOE-rA(Bz)-3'-oxy)-diisopropylphosphoramidite

DMTr-2'-O-EOE-rA(Bz)-3'-CE-Phosphoramidite

DMTr-2'-O-EOE-rG(iBu)-3'-CE-Phosphoramidite

DMTr-2'-O-EOE-5-Me-rC(Bz)-3'-CE-Phosphoramidite

DMTr-3'-O-MOE-5-Me-rC(Bz)-2'-CE-Phosphoramidite

DMTr-3'-O-MOE-rA(Bz)-2'-CE-Phosphoramidite

DMTr-3'-O-MOE-rG(iBu)-2'-CE-Phosphoramidite

DMTr-2'-O-MOEOE-5-Me-rC(Bz)-3'-CE-Phosphoramidite

DMTr-2'-O-MOEOE-rG(iBu)-3'-CE-Phosphoramidite

DMTr-2'-O-MOEOE-rA(Bz)-3'-CE-Phosphoramidite

DMTr-2'-O-Bu-rA(Bz)-3'-CE-Phosphoramidite

DMTr-2'-O-Et-rA(Bz)-3'-CE-Phosphoramidite

DMTr-2'-O-Bu-5-Me-rC(Bz)-3'-CE-Phosphoramidite

DMTr-2'-O-Et-5-Me-rC(Bz)-3'-CE-Phosphoramidite

DMTr-2'-O-Bu-rG(iBu)-3'-CE-Phosphoramidite

DMTr-2'-O-Et-rG(iBu)-3'-CE-Phosphoramidite

DMTr-2'-O-(Methyl behenate)-rC(Ac)-3'-CE-Phosphoramidite

DMTr-2'-O-C22-rU-3'-CE-Phosphoramidite

DMTr-2'-O-C6-rU-3'-CE-Phosphoramidite

Our Products

Liposome Products

MicroRNA Products

mRNA Products

siRNA Products

RNA Synthesis Reagents

Cap Analogs

CPGs for Oligo Synthesis

Nucleosides

Nucleotides

Phosphoramidites