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Pd-179

XantPhos Pd G2 | CAS Number: 1375325-77-1

Pd-185

(PCy₃) Pd G2 | CAS Number: 1353658-81-7

Pd-166

PdCl₂ [P(tBu)(Cy)₂]₂ | CAS Number: 104889-13-6

BPC-201

XPhos Pd G2 | CAS number: 1310584-14-5

BPC-203

SPhos Palladacycle 2nd Gen | CAS Number: 1375325-64-6

BPC-302

tBuXPhos Pd G3 | CAS Number: 1447963-75-8

GDH-101

Glucose dehydrogenase (GDH) catalyses the oxidation of D-glucose to D-glucolactone, while reducing in turn NAD+ or NADP+ to NADH and NADPH, respectively.

Pd-181

P(o-Tol)₃ Pd(crotyl)Cl | CAS Number: 1385042-42-1

ADH-110

An alcohol dehydrogenase (ADH) for the reduction of ketones and aldehydes to the corresponding alcohols.

ADH-150

An alcohol dehydrogenase (ADH) for the reduction of ketones and aldehydes to the corresponding alcohols

ADH-159

An alcohol dehydrogenase (ADH) for the reduction of ketones and aldehydes to the corresponding alcohols.

BPC-304

BrettPhos Pd G3 | CAS Number: 1470372-59-8

BPC-305

tBuBrettPhos Pd G3 | CAS Number: 1536473-72-9

BPC-306

RuPhos Pd G3 | CAS Number: 1445085-77-7

ADH-104

An alcohol dehydrogenase (ADH) for the reduction of ketones and aldehydes to the corresponding alcohols.

GDH-5

Glucose dehydrogenase (GDH) catalyses the oxidation of D-glucose to D-glucolactone, while reducing in turn NAD+ or NADP+ to NADH and NADPH, respectively.

Pd-132

PdCl₂(AmPhos)₂ | CAS Number: 887919-35-9

Pd-168

[P(tBu)₃] Palladacycle 2nd Gen | GenCAS Number: 1375325-71-5

STA-1

Aromatic and aliphatic primary amines can be obtained using our Transaminases

STA-113

Aromatic and aliphatic primary amines can be obtained using our Transaminases

STA-118

Aromatic and aliphatic primary amines can be obtained using our Transaminases

STA-120

Aromatic and aliphatic primary amines can be obtained using our Transaminases

STA-13

Aromatic and aliphatic primary amines can be obtained using our Transaminases

STA-121

Aromatic and aliphatic primary amines can be obtained using our Transaminases

STA-14

Aromatic and aliphatic primary amines can be obtained using our Transaminases

STA-2

Aromatic and aliphatic primary amines can be obtained using our Transaminases

RTA-40

Aromatic and aliphatic primary amines can be obtained using our Transaminases

RTA-25

Aromatic and aliphatic primary amines can be obtained using our Transaminases

RTA-45

Aromatic and aliphatic primary amines can be obtained using our Transaminases

RTA-58

Aromatic and aliphatic primary amines can be obtained using our Transaminases

IRED-3

An imine reductase (IRED) that catalyses the reductive amination of ketones with small aliphatic amines.

IRED-33

An imine reductase (IRED) that catalyses the reductive amination of ketones with small aliphatic amines.

IRED-18

An imine reductase (IRED) that catalyses the reductive amination of ketones with small aliphatic amines.

IRED-44

An imine reductase (IRED) that catalyses the reductive amination of ketones with small aliphatic amines.

IRED-49

An imine reductase (IRED) that catalyses the reductive amination of ketones with small aliphatic amines.

IRED-69

An imine reductase (IRED) that catalyses the reductive amination of ketones with small aliphatic amines.

IRED-72

An imine reductase (IRED) that catalyses the reductive amination of ketones with small aliphatic amines.

RTA-102

Aromatic and aliphatic primary amines can be obtained using our Transaminases

RTA-103

Aromatic and aliphatic primary amines can be obtained using our Transaminases

RTA-105

Aromatic and aliphatic primary amines can be obtained using our Transaminases

RTA-57

Aromatic and aliphatic primary amines can be obtained using our Transaminases

IRED-17

An imine reductase (IRED) that catalyses the reductive amination of ketones with small aliphatic amines.

IRED-1

An imine reductase (IRED) that catalyses the reductive amination of ketones with small aliphatic amines.

RTA-104

Aromatic and aliphatic primary amines can be obtained using our Transaminases

Johnson Matthey HY 2223 results presentation

PDF, 4.5 MB

AmDH-1

Aromatic and aliphatic primary amines can be obtained using Amine Dehydrogenses.

AmDH-3

Aromatic and aliphatic primary amines can be obtained using Amine Dehydrogenases.

AmDH-4

Aromatic and aliphatic primary amines can be obtained using Amine Dehydrogenases.

AmDH-2

Aromatic and aliphatic primary amines can be obtained using Amine Dehydrogenases.

AmDH-8

Aromatic and aliphatic primary amines can be obtained using Amine Dehydrogenases.

Nitinol products

Johnson Matthey is a leader in large diameter, thin wall and microlumen Nitinol tubing, commonly used in catheters, stents, and superelastic needles.

Pd-175

[tBuBrettPhos Pd(allyl)]OTf | CAS Number: 1798782-15-6

Chiral amines kit

Our chiral amines kit contains a comprehensive section of enzymes classes capable of transforming a variety of substrates into primary, secondary and tertiary amines.

Delivering against strategic objectives to drive value

News

Catalyst Technologies seminar - June 2023

Johnson Matthey is hosting a Catalyst Technologies seminar for investors and analysts. We will provide greater insight in the vital role our Catalyst Technologies business plays in the energy transition, which is creating significant growth opportunities for Johnson Matthey.

Precious metal and precision micromachined components

Medical device companies need a partner who can offer high quality, comprehensive solutions, to help manufacturers develop competitive technologies that are first to market.

Johnson Matthey and Honeywell partner to advance lower carbon hydrogen solutions

News

Q3 Trading Update 2016-17

News: Trading in line with expectations, full year outlook confirmed.

Johnson Matthey Chemist Wins Prestigious Royal Society of Chemistry Prize

Johnson Matthey Chemist Wins Prestigious Royal Society of Chemistry Prize

Johnson Matthey HY 2324 results presentation

PDF, 4 MB