Chemical Synthesis

Lead(II) perchlorate trihydrate may be used in the synthesis of calix[4]arene thioamides and macrocyclic lead(II) complexes.

100, 500 g in glass bottle

grade	ACS reagent
Quality Level	200,
assay	97.0-102.0% (ACS specification), 98%
form	crystals
reaction suitability	reagent type: oxidant
impurities	0.005% insolubles
pH	3.0-5.0 (25 °C, 5%)
anion traces	chloride (Cl^-): 0.01%
cation traces	Fe: 0.001%
SMILES string	O.O.O.[PbH2++].[O-]Cl(=O)(=O)=O.[O-]Cl(=O)(=O)=O
InChI	1S/2ClHO4.3H2O.Pb/c22-1(3,4)5;;;;/h2(H,2,3,4,5);3*1H2;/q;;;;;+2/p-2
Inchi Key	KKGGEAQRICYXNM-UHFFFAOYSA-L

pictograms	GHS03,GHS07,GHS08,GHS09
signalword	Danger
hcodes	H272 - H302 + H332 - H360Df - H373 - H410
pcodes	P201 - P210 - P273 - P301 + P312 + P330 - P304 + P340 + P312 - P308 + P313
RIDADR	UN 1470 6.1(5.1) / PGII
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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Lithium peroxide

Empirical Formula (Hill Notation):	Li₂O₂
CAS Number:	12031-80-0
Molecular Weight:	45.88
EC Number:	234-758-0
MDL number:	MFCD00016184
PubChem Substance ID:	24861460
NACRES:	NA.23

grade	technical grade
Quality Level	100,
assay	90%
form	powder
reaction suitability	reagent type: oxidant
Featured Industry	Battery Manufacturing
SMILES string	[Li+].[Li+].[O-][O-]
InChI	1S/2Li.O2/c;;1-2/q2*+1;-2
InChI key	HPGPEWYJWRWDTP-UHFFFAOYSA-N

pictograms	GHS03,GHS05
signalword	Danger
hcodes	H272 - H314
pcodes	P210 - P260 - P280 - P303 + P361 + P353 - P305 + P351 + P338 + P310
Personal Protective Equipment	Eyeshields,, Faceshields,, Gloves,, type P1 (EN143) respirator filter,, type P3 (EN 143) respirator cartridges,
RIDADR	UN 1472 5.1 / PGII
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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Luperox® 224, 2,4-Pentanedione peroxide solution 513555-500ML

Empirical Formula (Hill Notation):	C₁₀H₁₄O₆
CAS Number:	37187-22-7
Molecular Weight:	230.21
MDL number:	MFCD01742563
PubChem Substance ID:	24873699
NACRES:	NA.23

500 mL in poly bottle

Polymerization initiator

Product of Arkema Inc.
Luperox is a registered trademark of Arkema Inc.

Quality Level	100,
reaction suitability	reagent type: oxidant
concentration	~34 wt. % in 4-hydroxy-4-methyl-2-pentanone and N-methyl-2-pyrrolidone
refractive index	n20/D 1.439
bp	68 °C
density	1.068 g/mL at 25 °C
storage temp.	2-8°C
SMILES string	CC(=O)C(OOC(C(C)=O)C(C)=O)C(C)=O
InChI	1S/C10H14O6/c1-5(11)9(6(2)12)15-16-10(7(3)13)8(4)14/h9-10H,1-4H3
Inchi Key	ILENATNBFPBMHG-UHFFFAOYSA-N

pictograms	GHS02,GHS05,GHS07,GHS08
signalword	Danger
hcodes	H242 - H314 - H335 - H360FD
pcodes	P210 - P280 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338 - P370 + P378
Target Organs	Respiratory system
Personal Protective Equipment	Faceshields,, Gloves,, Goggles,, type ABEK (EN14387) respirator filter,
RIDADR	UN 3105A1 5.2
WGK Germany	WGK 1
Flash Point F	214.0 °F - closed cup
Flash Point C	101.11 °C - closed cup

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Luperox® A70S, Benzoyl peroxide 632651-500G

Empirical Formula (Hill Notation):	C₁₄H₁₀O₄
Linear Formula:	(C₆H₅CO)₂O₂
CAS Number:	94-36-0
Molecular Weight:	242.23
Beilstein/REAXYS Number:	984320
MDL number:	MFCD00003071
PubChem Substance ID:	24882501
NACRES:	NA.23

500 g in poly bottle

Widely used initiator, curing agent, and cross-linking agent in polymerization processes.

Luperox is a registered trademark of Arkema Inc.

Quality Level	100,
assay	70%
autoignition temp.	176 °F
reaction suitability	reagent type: oxidant
mp	105 °C (lit.)
storage temp.	2-8°C
SMILES string	O=C(OOC(=O)c1ccccc1)c2ccccc2
InChI	1S/C14H10O4/c15-13(11-7-3-1-4-8-11)17-18-14(16)12-9-5-2-6-10-12/h1-10H
InChI key	OMPJBNCRMGITSC-UHFFFAOYSA-N

Benzoyl peroxide belongs to a family of peroxides. It consists of two benzoyl groups bridged by peroxide link.Benzoyl peroxide has low solubility in water and ethanol.

pictograms	GHS02,GHS07
signalword	Danger
hcodes	H242 - H317 - H319
pcodes	P220 - P280 - P305 + P351 + P338 - P410 - P410 + P412 - P420
Personal Protective Equipment	Eyeshields,, Faceshields,, Gloves,, type N95 (US),
RIDADR	UN 3104A1 5.2
WGK Germany	WGK 1
Flash Point F	Not applicable
Flash Point C	Not applicable

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Luperox® A75, Benzoyl peroxide

Empirical Formula (Hill Notation):	C₁₄H₁₀O₄
Linear Formula:	(C₆H₅CO)₂O₂
CAS Number:	94-36-0
Molecular Weight:	242.23
Beilstein/REAXYS Number:	984320
MDL number:	MFCD00003071
PubChem Substance ID:	24873984
NACRES:	NA.23

5, 100, 500 g in poly bottle

Widely used initiator, curing agent, and cross-linking agent in polymerization processes.

Product of Arkema Inc.
Luperox is a registered trademark of Arkema Inc.

Quality Level	200,
assay	75%
autoignition temp.	176 °F
reaction suitability	reagent type: oxidant
mp	105 °C (lit.)
storage temp.	2-8°C
SMILES string	O=C(OOC(=O)c1ccccc1)c2ccccc2
InChI	1S/C14H10O4/c15-13(11-7-3-1-4-8-11)17-18-14(16)12-9-5-2-6-10-12/h1-10H
Inchi Key	OMPJBNCRMGITSC-UHFFFAOYSA-N

pictograms	GHS02,GHS07,GHS09
signalword	Danger
hcodes	H242 - H317 - H319 - H410
pcodes	P210 - P235 - P273 - P280 - P370 + P378 - P410
Personal Protective Equipment	dust mask type N95 (US),, Eyeshields,, Faceshields,, Gloves,, type P1 (EN143) respirator filter,, type P3 (EN 143) respirator cartridges,
RIDADR	UN 3104A1 5.2
WGK Germany	WGK 1
Flash Point F	Not applicable
Flash Point C	Not applicable

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Luperox® A75FP, Benzoyl peroxide, 75% remainder water 513474-500G

Empirical Formula (Hill Notation):	C₁₄H₁₀O₄
Linear Formula:	(C₆H₅CO)₂O₂
Molecular Weight:	242.23
Beilstein/REAXYS Number:	984320
MDL number:	MFCD00003071
PubChem Substance ID:	24873694
NACRES:	NA.23

500 g in poly bottle

Self Accelerating Decomposition Temperature (SADT): 71 °C

Luperox is a registered trademark of Arkema Inc.

Quality Level	200,
assay	75%
form	powder
contains	25 wt. % water as stabilizer
reaction suitability	reagent type: oxidant
mp	103 °C (lit.)
storage temp.	2-8°C
SMILES string	O=C(OOC(=O)c1ccccc1)c2ccccc2
InChI	1S/C14H10O4/c15-13(11-7-3-1-4-8-11)17-18-14(16)12-9-5-2-6-10-12/h1-10H
Inchi Key	OMPJBNCRMGITSC-UHFFFAOYSA-N

pictograms	GHS02,GHS07,GHS09
signalword	Danger
hcodes	H242 - H317 - H319 - H410
pcodes	P210 - P235 - P273 - P280 - P370 + P378 - P410
Personal Protective Equipment	Eyeshields,, Faceshields,, Gloves,, type N95 (US),
RIDADR	UN 3104A1 5.2
WGK Germany	WGK 1
Flash Point F	Not applicable
Flash Point C	Not applicable

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Luperox® ATC50, Benzoyl peroxide 513466-500ML

Empirical Formula (Hill Notation):	C₁₄H₁₀O₄
Linear Formula:	(C₆H₅CO)₂O₂
CAS Number:	94-36-0
Molecular Weight:	242.23
MDL number:	MFCD00003071
PubChem Substance ID:	24873693
NACRES:	NA.23

500 mL in poly bottle

Polymerization initiator

Product of Arkema Inc.
Luperox is a registered trademark of Arkema Inc.

Quality Level	100,
reaction suitability	reagent type: oxidant
concentration	~50 wt. % in tricresyl phosphate
density	1.16 g/mL at 25 °C (lit.)
storage temp.	2-8°C
SMILES string	O=C(OOC(=O)c1ccccc1)c2ccccc2
InChI	1S/C14H10O4/c15-13(11-7-3-1-4-8-11)17-18-14(16)12-9-5-2-6-10-12/h1-10H
Inchi Key	OMPJBNCRMGITSC-UHFFFAOYSA-N

100, 500 mL in poly bottle

pictograms	GHS02,GHS07,GHS08,GHS09
signalword	Warning
hcodes	H242 - H317 - H319 - H361f - H410
pcodes	P210 - P235 - P273 - P280 - P308 + P313 - P370 + P378
Personal Protective Equipment	dust mask type N95 (US),, Eyeshields,, Faceshields,, Gloves,, type P2 (EN 143) respirator cartridges,
RIDADR	UN 3108A4 5.2
WGK Germany	WGK 2
Flash Point F	230.0 °F - closed cup
Flash Point C	110 °C - closed cup

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Luperox® DHD-9, 2-Butanone peroxide solution

Empirical Formula (Hill Notation):	C₈H₁₈O₆
Linear Formula:	C₂H₅C(OOH)(CH₃)OOC(OOH)(CH₃)C₂H₅
CAS Number:	1338-23-4
Molecular Weight:	210.22
Beilstein/REAXYS Number:	1759757
MDL number:	MFCD00042641
PubChem Substance ID:	24874434
NACRES:	NA.23

Polymerization initiator

Product of Arkema Inc.
Luperox is a registered trademark of Arkema Inc.

Quality Level	100,
reaction suitability	reagent type: oxidant
concentration	~32 wt. % in phthalate-free plasticizer mixture
refractive index	n20/D 1.437
density	0.99 g/mL at 25 °C
storage temp.	2-8°C
SMILES string	CCC(C)(OO)OOC(C)(CC)OO
InChI	1S/C8H18O6/c1-5-7(3,11-9)13-14-8(4,6-2)12-10/h9-10H,5-6H2,1-4H3
InChI key	WFUGQJXVXHBTEM-UHFFFAOYSA-N

Luperox®DI, tert-Butyl peroxide has been used as a radical initiator to induce free radical polymerization. It has also been used as a cetane enhancer in a study to determine the phase behavior of carboxylate-based extended surfactant reverse micellar microemulsions with ethanol and vegetable oil/diesel blends.

pictograms	GHS02,GHS05,GHS08
signalword	Danger
hcodes	H242 - H314 - H361d - H412
pcodes	P210 - P273 - P280 - P303 + P361 + P353 - P305 + P351 + P338 - P370 + P378
Personal Protective Equipment	Faceshields,, Gloves,, Goggles,, type ABEK (EN14387) respirator filter,
RIDADR	UN 3105A5 5.2 / PGII
WGK Germany	WGK 1
Flash Point F	165.2 °F - closed cup
Flash Point C	74 °C - closed cup

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Luperox® DI, tert-Butyl peroxide

Empirical Formula (Hill Notation):	C₈H₁₈O₂
Linear Formula:	(CH₃)₃COOC(CH₃)₃
CAS Number:	110-05-4
Molecular Weight:	146.23
Beilstein/REAXYS Number:	1735581
EC Number:	203-733-6
MDL number:	MFCD00008803
PubChem Substance ID:	24850244
NACRES:	NA.22

5, 250 mL in poly bottle
1 L in poly bottle

Product of Arkema Inc.
Luperox is a registered trademark of Arkema Inc.

vapor pressure	40 mmHg ( 20 °C)
Quality Level	100,
assay	98%
reaction suitability	reagent type: oxidant
refractive index	n20/D 1.3891 (lit.)
bp	109-110 °C (lit.)
density	0.796 g/mL at 25 °C (lit.)
storage temp.	2-8°C
SMILES string	CC(C)(C)OOC(C)(C)C
InChI	1S/C8H18O2/c1-7(2,3)9-10-8(4,5)6/h1-6H3
Inchi Key	LSXWFXONGKSEMY-UHFFFAOYSA-N

5, 100, 500 g in poly bottle

pictograms	GHS02,GHS08
signalword	Danger
hcodes	H225 - H242 - H341 - H412
pcodes	P210 - P220 - P273 - P280 - P410 - P411 + P235
Personal Protective Equipment	Eyeshields,, Faceshields,, Gloves,, type ABEK (EN14387) respirator filter,
RIDADR	UN 3107A2 5.2
WGK Germany	WGK 1
Flash Point F	42.8 °F - closed cup
Flash Point C	6 °C - closed cup

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Luperox® LP, Lauroyl peroxide

Empirical Formula (Hill Notation):	C₂₄H₄₆O₄
Linear Formula:	[CH₃(CH₂)₁₀CO]₂O₂
CAS Number:	105-74-8
Molecular Weight:	398.62
Beilstein/REAXYS Number:	1804936
EC Number:	203-326-3
MDL number:	MFCD00008964
PubChem Substance ID:	24857486
NACRES:	NA.23

Product of Arkema Inc.
Luperox is a registered trademark of Arkema Inc.

vapor density	13.7 (vs air)
assay	98%
reaction suitability	reagent type: oxidant
mp	53-57 °C (lit.)
storage temp.	2-8°C
SMILES string	CCCCCCCCCCCC(=O)OOC(=O)CCCCCCCCCCC
InChI	1S/C24H46O4/c1-3-5-7-9-11-13-15-17-19-21-23(25)27-28-24(26)22-20-18-16-14-12-10-8-6-4-2/h3-22H2,1-2H3
InChI key	YIVJZNGAASQVEM-UHFFFAOYSA-N

We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product MMPP is an alternative to widely used oxidant MCPBA as it is cheap, stable in the solid state, safer in handling and easier to use and thus aligns with the principle "Designing Safer Chemicals". For more information see the below articles.
Magnesium bis(monoperoxyphthalate) hexahydrate as mild and efficient oxidant for the synthesis of selenones,.
Magnesium Bis(monoperoxyphthalate) Hexahydrate (MMPP),.
Highly efficient epoxidation of unsaturated steroids using magnesium bis(monoperoxyphthalate) hexahydrate,.

pictograms	GHS02
signalword	Danger
hcodes	H242
pcodes	P210 - P234 - P235 - P280 - P370 + P378 - P410
Personal Protective Equipment	Eyeshields,, Gloves,, type P1 (EN143) respirator filter,, type P3 (EN 143) respirator cartridges,
RIDADR	UN 3106A2 5.2 / PGII
WGK Germany	WGK 1
Flash Point F	Not applicable
Flash Point C	Not applicable

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Magnesium bis(monoperoxyphthalate) hexahydrate

Empirical Formula (Hill Notation):	C₁₆H₁₀MgO₁₀ · 6H₂O
Linear Formula:	(HO₂CC₆H₄CO₃)₂Mg·6H₂O
Molecular Weight:	494.64
EC Number:	279-013-0
MDL number:	MFCD00149614
PubChem Substance ID:	24857092
NACRES:	NA.22

A safer, greener oxidizing reagent that is a suitable replacement for peroxycarboxylic acids and is capable of effecting many types of oxidation reactions.
Oxidation Reactions Using Magnesium Monoperphthalate: A Comparison with m-Chloroperoxybenzoic Acid,
Reagent for:

Trans-diaxial hydroxylation under bismuth(III) triflate catalyst
Oxidation rections under mild conditions
Epoxidation of unsaturated steroids
Synthesis of ring-B oxygenated steroids as anticancer agents

100 g in poly bottle

grade	technical grade
Quality Level	200,
assay	80%
reaction suitability	reagent type: oxidant
greener alternative product characteristics	Designing Safer Chemicals Learn more about the Principles of Green Chemistry,.
mp	93 °C (dec.) (lit.)
greener alternative category	Aligned,
SMILES string	O.O.O.O.O.O.OOC(=O)c1ccccc1C(=O)O[Mg]OC(=O)c2ccccc2C(=O)OO
InChI	1S/2C8H6O5.Mg.6H2O/c29-7(10)5-3-1-2-4-6(5)8(11)13-12;;;;;;;/h21-4,12H,(H,9,10);;6*1H2/q;;+2;;;;;;/p-2
InChI key	WWOYCMCZTZTIGU-UHFFFAOYSA-L

Magnesium monoperoxyphthalate hexahydrate is an organic peroxide used in many oxidation reactions. It exhibits non-deflagrating and non-shock-sensitive properties and also used as a surface disinfectant.

pictograms	GHS07
signalword	Warning
hcodes	H312 - H315 - H319 - H335
pcodes	P280 - P302 + P352 + P312 - P305 + P351 + P338
Target Organs	Respiratory system
Personal Protective Equipment	dust mask type N95 (US),, Eyeshields,, Gloves,
RIDADR	NONH for all modes of transport
WGK Germany	WGK 2
Flash Point F	Not applicable
Flash Point C	Not applicable

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Magnesium monoperoxyphthalate hexahydrate

Empirical Formula (Hill Notation):	C₁₆H₁₀MgO₁₀ · 6H₂O
Linear Formula:	(HO₂CC₆H₄CO₃)₂Mg·6H₂O
Molecular Weight:	494.64
EC Number:	279-013-0
MDL number:	MFCD00149614
PubChem Substance ID:	57652217
NACRES:	NA.22

Reagent for:

Trans-diaxial hydroxylation under bismuth(III) triflate catalyst
Oxidation rections under mild conditions
Epoxidation of unsaturated steroids
Synthesis of ring-B oxygenated steroids as anticancer agents

50, 250 g in poly bottle
1 kg in poly bottle

Versatile oxidant soluble in water and the lower alcohols.; Oxidations are carried out in homogenous solution (alcohol, aqueous alcohol) or in a two-phase system under PTC (chloroform-water)

Quality Level	200,
grade	technical
assay	~80% (RT)
reaction suitability	reagent type: oxidant
mp	93 °C (dec.) (lit.)
SMILES string	O.O.O.O.O.O.OOC(=O)c1ccccc1C(=O)O[Mg]OC(=O)c2ccccc2C(=O)OO
InChI	1S/2C8H6O5.Mg.6H2O/c29-7(10)5-3-1-2-4-6(5)8(11)13-12;;;;;;;/h21-4,12H,(H,9,10);;6*1H2/q;;+2;;;;;;/p-2
InChI key	WWOYCMCZTZTIGU-UHFFFAOYSA-L

Magnesium perchlorate (Mg(ClO4)2) is widely used as drying agent for gases. It can remove water from gases (with no organic contaminants) at the rate of 0.001mgwater/l.

pictograms	GHS07
signalword	Warning
hcodes	H312 - H315 - H319 - H335
pcodes	P280 - P302 + P352 + P312 - P305 + P351 + P338
Target Organs	Respiratory system
Personal Protective Equipment	dust mask type N95 (US),, Eyeshields,, Gloves,
RIDADR	NONH for all modes of transport
WGK Germany	WGK 2
Flash Point F	Not applicable
Flash Point C	Not applicable

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Magnesium perchlorate

Empirical Formula (Hill Notation):	Cl₂MgO₈
Linear Formula:	Mg(ClO₄)₂
CAS Number:	10034-81-8
Molecular Weight:	223.21
EC Number:	233-108-3
MDL number:	MFCD00011102
PubChem Substance ID:	329752290
NACRES:	NB.24

Magnesium perchlorate may be used as a catalyst in the synthesis of the following compounds:

-Aminophosphonates via three-component reaction between an amine, an aldehyde or a ketone and a di-/trialkyl phosphite.
Imines and phenylhydrazones by the condensation of carbonyl compounds with amines and phenylhydrazine.
Knoevenagel adducts via Knoevenagel condensation between -diketones and aliphatic or aromatic aldehydes.

It may also be used to catalyze the protection of alcohols as t-butyl ethers.
Magnesium perchlorate (Mg(ClO4)2) may be employed as a catalyst in the following studies:

Preparation of -aminophosphonates.
Enantioselective Diels-Alder reaction between cyclopentadiene and 3-acryloyl-1,3-oxazolin-2-one.
Preparation of imines and phenylhydrazones.
Protection of alcohols in the form of t-butyl ethers.

500 g in glass bottle
5 g in glass bottle
100 g in poly bottle

grade	ACS reagent
Quality Level	200,
assay	>10.0% Mg basis (EDTA titration)
form	flakes, powder, chunks or granules
reaction suitability	reagent type: oxidant
impurities	≤0.005 meq/g Titr. free acid, ≤0.025 meq/g Titr. base
loss	≤8% loss on drying
suitability	passes test for moisture absorption
SMILES string	[Mg++].[O-]Cl(=O)(=O)=O.[O-]Cl(=O)(=O)=O
InChI	1S/2ClHO4.Mg/c22-1(3,4)5;/h2(H,2,3,4,5);/q;;+2/p-2
InChI key	MPCRDALPQLDDFX-UHFFFAOYSA-L

Magnesium perchlorate hexahydrate is a highly hygroscopic metal hydrate that can be dehydrated to prepare anhydrous magnesium perchlorate. It can be used as an electrophilic catalyst for non-enzymic reduction of synthetic dihydropyridines. It may also be used in the formation of magnesium ion batteries.

pictograms	GHS03,GHS07
signalword	Danger
hcodes	H272 - H315 - H319 - H335
pcodes	P210 - P302 + P352 - P305 + P351 + P338
Target Organs	Respiratory system
RIDADR	UN 1475 5.1 / PGII
WGK Germany	WGK 1
Flash Point F	Not applicable
Flash Point C	Not applicable

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Magnesium perchlorate hexahydrate

Empirical Formula (Hill Notation):	Cl₂MgO₈ · 6H₂O
Linear Formula:	Mg(ClO₄)₂·6H₂O
CAS Number:	13446-19-0
Molecular Weight:	331.30
EC Number:	233-108-3
MDL number:	MFCD00149778
PubChem Substance ID:	24858726
NACRES:	NA.23

100, 500 g in glass bottle

Quality Level	100,
assay	99%
form	crystalline
reaction suitability	reagent type: oxidant
SMILES string	[Mg++].[H]O[H].[H]O[H].[H]O[H].[H]O[H].[H]O[H].[H]O[H].[O-]Cl(=O)(=O)=O.[O-]Cl(=O)(=O)=O
InChI	1S/2ClHO4.Mg.6H2O/c22-1(3,4)5;;;;;;;/h2(H,2,3,4,5);;6*1H2/q;;+2;;;;;;/p-2
InChI key	MGBDNCBRZIMSDZ-UHFFFAOYSA-L

pictograms	GHS03,GHS07
signalword	Danger
hcodes	H272 - H315 - H319 - H335
pcodes	P210 - P302 + P352 - P305 + P351 + P338
Target Organs	Respiratory system
Personal Protective Equipment	dust mask type N95 (US),, Eyeshields,, Gloves,, type P1 (EN143) respirator filter,, type P3 (EN 143) respirator cartridges,
RIDADR	UN 1475 5.1 / PGII
WGK Germany	WGK 1
Flash Point F	Not applicable
Flash Point C	Not applicable

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Magnesium peroxide complex

Linear Formula:	MgO₂· xMgO
CAS Number:	1335-26-8
EC Number:	215-627-7
PubChem Substance ID:	24867150
NACRES:	NA.23

grade	technical grade
Quality Level	100,
composition	Mg, 30% , MgO₂, 24-28%
reaction suitability	reagent type: oxidant
Featured Industry	Battery Manufacturing
SMILES string	[Mg++].[O-][O-].O=[Mg]
InChI	1S/2Mg.O2.O/c;;1-2;/q;+2;-2;
InChI key	IODFUUWCSICZNX-UHFFFAOYSA-N

Starting material for homometallic, trinuclear heteroscorpionate complexes applied in studies of electronic and magnetic properties.

pictograms	GHS03
signalword	Danger
hcodes	H272
pcodes	P210
Personal Protective Equipment	Eyeshields,, Gloves,, type P1 (EN143) respirator filter,, type P3 (EN 143) respirator cartridges,
RIDADR	UN 1476 5.1 / PGII
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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Manganese(II) perchlorate hydrate

Empirical Formula (Hill Notation):	Cl₂MnO₈ · xH₂O
Linear Formula:	Mn(ClO₄)₂·xH₂O
CAS Number:	698999-57-4
Molecular Weight:	253.84 (anhydrous basis)
MDL number:	MFCD00150254
PubChem Substance ID:	24862073
NACRES:	NA.23

100 g in poly bottle

Quality Level	100,
assay	99%
form	crystalline
reaction suitability	reagent type: oxidant
Featured Industry	Battery Manufacturing
SMILES string	O.[Mn++].[O-]Cl(=O)(=O)=O.[O-]Cl(=O)(=O)=O
InChI	1S/2ClHO4.Mn.H2O/c22-1(3,4)5;;/h2(H,2,3,4,5);;1H2/q;;+2;/p-2
Inchi Key	VAZHKDVMMUBWIG-UHFFFAOYSA-L

Assay (iodometric, calc. on dried substance): 90.0 %
Loss on drying: 3.5 %
Oxidation Activity: passes test

pictograms	GHS03,GHS07
signalword	Danger
hcodes	H272 - H315 - H319 - H335
pcodes	P210 - P302 + P352 - P305 + P351 + P338
Target Organs	Respiratory system
Personal Protective Equipment	dust mask type N95 (US),, Eyeshields,, Gloves,, type P1 (EN143) respirator filter,, type P3 (EN 143) respirator cartridges,
RIDADR	UN 1481 5.1 / PGII
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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Manganese(IV) oxide

Empirical Formula (Hill Notation):	MnO₂
CAS Number:	1313-13-9
Molecular Weight:	86.94
MDL number:	MFCD00003463
EC Index Number:	215-202-6

Кат. номер
8059589050
8059581000
8059589999
8059580100
8.05958.9050
8.05958.0100
8.05958.1000

Analysis Note

storage conditions	Store below +30°C.
Quality Level	200,
potency	>3478 mg/kg LD₅₀, oral (Rat)
reaction suitability	reagent type: oxidant
solubility	insoluble <0.001 g/L
density	5.21 g/cm³ at 21 °C
bulk density	600800 kg/m³
storage temp.	2-30°C
InChI	1S/Mn.2O
InChI key	NUJOXMJBOLGQSY-UHFFFAOYSA-N

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Mercury(II) perchlorate hydrate

Empirical Formula (Hill Notation):	Cl₂HgO₈ · xH₂O
Linear Formula:	Hg(ClO₄)₂·xH₂O
CAS Number:	304656-34-6
Molecular Weight:	399.49 (anhydrous basis)
EC Number:	231-525-5
MDL number:	MFCD00673716
PubChem Substance ID:	24858727
NACRES:	NA.23

Quality Level	200,
assay	98%
form	solid
composition	Degree of hydration, 3-5 , Hg, 42-45%
reaction suitability	reagent type: oxidant
storage temp.	−20°C
SMILES string	O.[Hg++].[O-]Cl(=O)(=O)=O.[O-]Cl(=O)(=O)=O
InChI	1S/2ClHO4.Hg.H2O/c22-1(3,4)5;;/h2(H,2,3,4,5);;1H2/q;;+2;/p-2
InChI key	OOYSCVKOXPZTGW-UHFFFAOYSA-L

pictograms	GHS03,GHS06,GHS08,GHS09
signalword	Danger
hcodes	H272 - H300 + H310 + H330 - H373 - H410
pcodes	P210 - P262 - P280 - P301 + P310 + P330 - P302 + P352 + P310 - P304 + P340 + P310
Personal Protective Equipment	dust mask type N95 (US),, Eyeshields,, Faceshields,, Gloves,, type P2 (EN 143) respirator cartridges,
RIDADR	UN 3086 5.1(6.1) / PGII
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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Methyl chlorooxoacetate

Empirical Formula (Hill Notation):	C₃H₃ClO₃
Linear Formula:	ClCOCOOCH₃
CAS Number:	5781-53-3
Molecular Weight:	122.51
Beilstein/REAXYS Number:	1071541
EC Number:	227-307-4
MDL number:	MFCD00000705
PubChem Substance ID:	24849133
NACRES:	NA.22

Reactant involved in:

Regioselective synthesis of fused coumarins
Cyclization to form substituted isoxazoles and heterocycles
Intramolecular Wittig reactions
Silyl enol ether acylation
Iron-mediated cleavage of C-C bonds

5, 10, 50 g in glass bottle

Quality Level	200,
assay	96%
reaction suitability	reagent type: oxidant
refractive index	n20/D 1.419 (lit.)
bp	118-120 °C (lit.)
density	1.332 g/mL at 25 °C (lit.)
SMILES string	COC(=O)C(Cl)=O
InChI	1S/C3H3ClO3/c1-7-3(6)2(4)5/h1H3
Inchi Key	ZXUQEPZWVQIOJE-UHFFFAOYSA-N

mIBX (modified 2-iodoxybenzoic acid), a water-soluble hypervalent iodine compound, can be prepared from 3-nitrophthalic acid. mIBX is an environment-friendly oxidizing agent that allows selective oxidation of allylic and benzylic alcohols in water.

pictograms	GHS02,GHS05,GHS07
signalword	Danger
hcodes	H226 - H314 - H335
pcodes	P210 - P280 - P303 + P361 + P353 - P305 + P351 + P338 + P310
Target Organs	Respiratory system
Personal Protective Equipment	Faceshields,, Gloves,, Goggles,, type ABEK (EN14387) respirator filter,
RIDADR	UN 2920 3(8) / PGII
WGK Germany	WGK 3
Flash Point F	114.8 °F - closed cup
Flash Point C	46 °C - closed cup

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mIBX

Empirical Formula (Hill Notation):	C₈H₅IO₆
Molecular Weight:	324.03
MDL number:	MFCD03839922
PubChem Substance ID:	329768281
NACRES:	NA.22

1, 5 g in glass bottle

reaction suitability	reagent type: oxidant
storage temp.	−20°C
SMILES string	O=C(O1)C2=C(C(O)=O)C=CC=C2I1(O)=O
InChI	1S/C8H5IO6/c10-7(11)4-2-1-3-5-6(4)8(12)15-9(5,13)14/h1-3H,(H,10,11)(H,13,14)
InChI key	YGABLFBBILUMGY-UHFFFAOYSA-N

Assay (iodometric): 99.0 %
Identity (IR): passes test

pictograms	GHS07
signalword	Warning
hcodes	H315 - H319 - H335
pcodes	P302 + P352 - P305 + P351 + P338
Target Organs	Respiratory system
RIDADR	NONH for all modes of transport
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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N-Bromosuccinimide

Empirical Formula (Hill Notation):	C₄H₄BrNO₂
CAS Number:	128-08-5
Molecular Weight:	177.98
MDL number:	MFCD00005510
EC Index Number:	204-877-2

Кат. номер
8019490250
8019491000
8019490005
8019499025
8.01949.0005
US1801949/1000
8.01949.1000
8.01949.0250

Analysis Note

Used in investigations of the toxicity response of electroactive microbial biofilms

Catalyst for rearrangement of aziridinofullerenes to azafulleroids

Oxidizing agent for polymerization of thiophenol, synthesis of o-aminobenzenesulfonic acids and ciproflaxin

Decontaminant for mustard

storage conditions	Store at +2°C to +8°C.
vapor pressure	14.8 hPa ( 20 °C)
Quality Level	200,
potency	>2000 mg/kg LD₅₀, oral (Rat)
reaction suitability	reagent type: oxidant
mp	174-179 °C
solubility	14.8 g/L (decomposition)
density	2.1 g/cm³ at 20 °C
bulk density	750 kg/m³
storage temp.	2-8°C
InChI	1S/C4H4BrNO2/c5-6-3(7)1-2-4(6)8/h1-2H2
Inchi Key	PCLIMKBDDGJMGD-UHFFFAOYSA-N

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N-Chlorobenzenesulfonamide sodium salt

Empirical Formula (Hill Notation):	C₆H₅ClNNaO₂S · xH₂O
Linear Formula:	C₆H₅SO₂NClNa · aq
CAS Number:	127-52-6
Molecular Weight:	213.62 (anhydrous basis)
Beilstein/REAXYS Number:	3599287
EC Number:	204-847-9
MDL number:	MFCD00149552
PubChem Substance ID:	57648029
NACRES:	NA.22

100, 500 g in poly bottle

Review

Quality Level	100,
assay	~28% active chlorine basis
reaction suitability	reagent type: oxidant
SMILES string	O.[Na]N(Cl)S(=O)(=O)c1ccccc1
InChI	1S/C6H5ClNO2S.Na.H2O/c7-8-11(9,10)6-4-2-1-3-5-6;;/h1-5H;;1H2/q-1;+1;
InChI key	YVICIJMKLANTNN-UHFFFAOYSA-N

Assay (iodometric): 98,0 %(m)
Melting range (lower value): 146 °C
Melting range (upper value): 151 °C
Identity (IR): conforms

pictograms	GHS05,GHS07,GHS08
signalword	Danger
hcodes	H302 - H314 - H334
pcodes	P261 - P280 - P305 + P351 + P338 - P310
Supp Hazards	EUH029
Personal Protective Equipment	Eyeshields,, Faceshields,, Gloves,, type P1 (EN143) respirator filter,, type P3 (EN 143) respirator cartridges,
RIDADR	UN 3263 8 / PGII
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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N-Chlorosuccinimide

Empirical Formula (Hill Notation):	C₄H₄ClNO₂
CAS Number:	128-09-6
Molecular Weight:	133.53
MDL number:	MFCD00005511
EC Index Number:	204-878-8

N-Hydroxytetrachlorophthalimide (TCNHPI) is an aryl-tetrahalogenated N-hydroxyphthalimide derivative. In combination with 1,4-diamino-2,3-dichloroanthraquinone (DADCAQ), it forms an efficient catalytic system for the oxidation of aromatic hydrocarbons using molecular oxygen under metal-free and aerobic conditions.

storage conditions	Store at +2°C to +8°C.
Quality Level	200,
potency	1000 mg/kg LD₅₀, oral (Rat)
reaction suitability	reagent type: oxidant
bp	216.5 °C
mp	146-151 °C
transition temp	flash point >110 °C
density	1.65 g/cm³ at 20 °C
bulk density	600 kg/m³
storage temp.	2-8°C
InChI	1S/C4H4ClNO2/c5-6-3(7)1-2-4(6)8/h1-2H2
InChI key	JRNVZBWKYDBUCA-UHFFFAOYSA-N

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N-Hydroxytetrachlorophthalimide

Empirical Formula (Hill Notation):	C₈HCl₄NO₃
CAS Number:	85342-65-0
Molecular Weight:	300.91
PubChem Substance ID:	329772721

New reagent enabling the electrochemical allylic C-H oxidation reaction developed by the Baran group. This method provides a scalable and sustainable alternative to current strategies based on toxic reagents or precious metals.

1, 10 g in glass bottle
50 g in poly bottle

Electrochemical Allylic C–H Oxidation with N-Hydroxytetrachlorophthalimide (TCNHPI),
Scalable and sustainable electrochemical allylic C–H oxidation,
A general alkyl-alkyl cross-coupling enabled by redox-active esters and alkylzinc reagents,
Nickel-Catalyzed Cross-Coupling of Redox-Active Esters with Boronic Acids,
Practical Ni-Catalyzed Aryl-Alkyl Cross-Coupling of Secondary Redox-Active Esters,

form	powder
Quality Level	100,
reaction suitability	reagent type: oxidant
SMILES string	O=C1N(O)C(C2=C(Cl)C(Cl)=C(Cl)C(Cl)=C21)=O
InChI	1S/C8HCl4NO3/c9-3-1-2(4(10)6(12)5(3)11)8(15)13(16)7(1)14/h16H
InChI key	UTRBHXSKVVPTLY-UHFFFAOYSA-N

In the presence of NCS, this sulfenamide catalyzes the mild and selective oxidation of primary and secondary alcohols to the respective aldehydes and ketones.

pictograms	GHS06
signalword	Danger
hcodes	H301
pcodes	P301 + P330 + P331 + P310
RIDADR	UN 2811 6.1 / PGIII
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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N-tert-Butylbenzenesulfenamide

Empirical Formula (Hill Notation):	C₁₀H₁₅NS
CAS Number:	19117-31-8
Molecular Weight:	181.30
MDL number:	MFCD03844776
PubChem Substance ID:	24885655
NACRES:	NA.22

Anti-SN2 Mitsunobu reaction with chiral hydroxy-alpha-alkenylsilanes to give vinylsilanes
Anodic oxidation reactions

1 g in glass bottle

Quality Level	100,
assay	97%
reaction suitability	reagent type: oxidant
refractive index	n20/D 1.5457
bp	57-60 °C/0.3 mmHg
density	0.997 g/mL at 25 °C
SMILES string	CC(C)(C)NSc1ccccc1
InChI	1S/C10H15NS/c1-10(2,3)11-12-9-7-5-4-6-8-9/h4-8,11H,1-3H3
Inchi Key	AAQBFMPKCDTAJD-UHFFFAOYSA-N

Used to study differences in reactivity trends for carbon monoxide catalyzed oxidation caused by anionic transition metal oxide clusters

Reagent:

Personal Protective Equipment	Eyeshields,, Gloves,, multi-purpose combination respirator cartridge (US),
RIDADR	UN 3334
WGK Germany	WGK 3
Flash Point F	205.0 °F - closed cup
Flash Point C	96.11 °C - closed cup

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Nickel peroxide

Empirical Formula (Hill Notation):	NiO₂
CAS Number:	12035-36-8
Molecular Weight:	90.69
EC Number:	234-823-3
MDL number:	MFCD00011143
PubChem Substance ID:	57652407
NACRES:	NA.22

One-dimensional oxide-metal hybrid structures and site-specific enhanced reactivity for CO oxidation
Microwave induced catalytic degradation of crystal violet

For solvent-free oxidation of alcohols†
For chemoselective oxidation of organic compounds using inductive heating
To improve the synthesis of methoxy cephalosporins intermediate

5 g in poly bottle

Oxidant for the transformation of alcohols into acids and hydrazones into diazoalkanes

Quality Level	100,
grade	oxidizing agent, technical
assay	~30% active peroxide basis
reaction suitability	core: nickel, reagent type: catalyst, reagent type: oxidant
SMILES string	O=[Ni]O[Ni]=O
InChI	1S/2Ni.3O
Inchi Key	PZFKDUMHDHEBLD-UHFFFAOYSA-N

Starting material for homometallic, trinuclear heteroscorpionate complexes applied in studies of electronic and magnetic properties.

pictograms	GHS03,GHS07,GHS08
signalword	Danger
hcodes	H272 - H317 - H350i - H372 - H413
pcodes	P201 - P210 - P273 - P280 - P302 + P352 - P308 + P313
Personal Protective Equipment	Eyeshields,, Faceshields,, Gloves,, type P1 (EN143) respirator filter,, type P3 (EN 143) respirator cartridges,
RIDADR	UN 1479 5.1 / PGII
WGK Germany	WGK 1
Flash Point F	Not applicable
Flash Point C	Not applicable

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Nickel(II) perchlorate hexahydrate

Empirical Formula (Hill Notation):	Cl₂NiO₈ · 6H₂O
Linear Formula:	Ni(ClO₄)₂ · 6H₂O
CAS Number:	13520-61-1
Molecular Weight:	365.69
EC Number:	237-124-1
MDL number:	MFCD00149804
PubChem Substance ID:	24858728
NACRES:	NA.23

5, 100, 500 g in glass bottle

Quality Level	100,
assay	15.2-16.9% Ni basis (EDTA titration)
form	crystalline
reaction suitability	reagent type: oxidant
mp	140 °C (lit.)
Featured Industry	Battery Manufacturing
SMILES string	O.O.O.O.O.O.[Ni++].[O-]Cl(=O)(=O)=O.[O-]Cl(=O)(=O)=O
InChI	1S/2ClHO4.Ni.6H2O/c22-1(3,4)5;;;;;;;/h2(H,2,3,4,5);;6*1H2/q;;+2;;;;;;/p-2
Inchi Key	WHGYCGOFTBFDLW-UHFFFAOYSA-L

We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product has been enhanced for energy efficiency. Find details here,.

pictograms	GHS05,GHS08,GHS09
signalword	Danger
hcodes	H314 - H317 - H334 - H341 - H350 - H360 - H372 - H410
pcodes	P260 - P273 - P280 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338
Personal Protective Equipment	Eyeshields,, Faceshields,, Gloves,, type P1 (EN143) respirator filter,, type P2 (EN 143) respirator cartridges,, type P3 (EN 143) respirator cartridges,
RIDADR	UN1481 - class 5.1 - PG 2 - EHS - Perchlorates, inorganic, n.o.s., HI: A, S (not BR)
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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Nickel(II) peroxide hydrate

Empirical Formula (Hill Notation):	NiO₂ · xH₂O
CAS Number:	86676-91-7
Molecular Weight:	90.69 (anhydrous basis)
EC Number:	215-217-8
MDL number:	MFCD00171392
PubChem Substance ID:	24862401
NACRES:	NA.23

1, 10 g in glass bottle

Quality Level	100,
reaction suitability	reagent type: catalyst core: nickel, reagent type: oxidant
greener alternative product characteristics	Design for Energy Efficiency Learn more about the Principles of Green Chemistry,.
Featured Industry	Battery Manufacturing
SMILES string	O.O1O[Ni]1
InChI	1S/Ni.O2.H2O/c;1-2;/h;;1H2/q+2;-2;
InChI key	WFGXJOHFKNQUMN-UHFFFAOYSA-N

Nitrosyl tetrafluoroborate is an efficient nitrosating and diazotizing agent. It reacts with alcohols and secondary amines to yield alkyl nitrites and nitrosamines, respectively. It reacts with primary amines to yield diazonium tetrafluoroborates. NOBF4 is also a mild oxidant and commonly used for single electron transfer oxidation.

pictograms	GHS03,GHS07,GHS08
signalword	Danger
hcodes	H272 - H317 - H350i - H372 - H413
pcodes	P201 - P210 - P273 - P280 - P302 + P352 - P308 + P313
Personal Protective Equipment	Eyeshields,, Faceshields,, Gloves,, type P1 (EN143) respirator filter,, type P3 (EN 143) respirator cartridges,
RIDADR	UN 1483 5.1 / PGII
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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Nitrosyl tetrafluoroborate

Empirical Formula (Hill Notation):	BF₄NO
Linear Formula:	NOBF₄
CAS Number:	14635-75-7
Molecular Weight:	116.81
EC Number:	238-679-2
MDL number:	MFCD00011433
PubChem Substance ID:	24850360
NACRES:	NA.22

5, 25, 50 g in amber poly bottle

Quality Level	100,
assay	95%
reaction suitability	reagent type: oxidant
storage temp.	2-8°C
SMILES string	N#[O+].F[B-](F)(F)F
InChI	1S/BF4.NO/c2-1(3,4)5;1-2/q-1;+1
InChI key	KGCNVGDHOSFKFT-UHFFFAOYSA-N

Osmium tetroxide (OsO4) is widely employed as a catalyst in various organic reactions. Stereochemical aspects of the OsO4 assisted oxidation of allylic alcohols and their derivatives have been reported. Its reaction with olefins has been investigated. It participates as a catalyst for oxidizing fluoroquinolones, via reaction with potassium hexacyanoferrate(III) in alkaline medium. Kinetics of this oxidation reaction was studied.

pictograms	GHS05
signalword	Danger
hcodes	H314
pcodes	P260 - P280 - P301 + P330 + P331 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338
Personal Protective Equipment	Eyeshields,, Faceshields,, Gloves,, type P1 (EN143) respirator filter,, type P3 (EN 143) respirator cartridges,
RIDADR	UN 3260 8 / PGII
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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Osmium tetroxide

Empirical Formula (Hill Notation):	O₄Os
Linear Formula:	OsO₄
CAS Number:	20816-12-0
Molecular Weight:	254.23
EC Number:	244-058-7
MDL number:	MFCD00011150
PubChem Substance ID:	329751973
NACRES:	NA.55

Widely used oxidizer for visualizing cells in microscopy. Promotes oxidative cleavage of graphene layers in carbon nanotubes creating the possibility of opening ′windows′ in fullerene cages.
Osmium tetroxide may be employed as a catalyst for the hydroxylation of sterically hindered olefins.
Osmium tetroxide may be used in the following processes:

To promote the lactonization of alkenols to lactones.
To mediate the selective oxidative cleavage of olefins by oxone to form the corresponding ketones or carboxylic acids.
Dihydroxylation of mono-trans-di, and trisubstituted olefins to form 1,2-diols with high enantioselectivity in the presence of chiral amines.

250, 500 mg in ampule
1 g in ampule

ReagentPlus is a registered trademark of Sigma-Aldrich Co. LLC

Quality Level	200
vapor density	8.8 (vs air)
vapor pressure	7 mmHg ( 20 °C)
product line	ReagentPlus^®
assay	99.8%
form	crystalline, powder
reaction suitability	reagent type: oxidant
bp	130 °C (lit.)
mp	39.5-41 °C (lit.)
storage temp.	2-8°C
SMILES string	O=[Os](=O)(=O)=O
InChI	1S/4O.Os
Inchi Key	VUVGYHUDAICLFK-UHFFFAOYSA-N

Osmium tetroxide solution has been used as a fixative in scanning and transmission electron microscopy.

pictograms	GHS05,GHS06
signalword	Danger
hcodes	H300 + H310 + H330 - H314
pcodes	P260 - P270 - P280 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338
RIDADR	UN 2471 6.1 / PGI
WGK Germany	WGK 1

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Osmium tetroxide solution

Empirical Formula (Hill Notation):	O₄Os
Linear Formula:	OsO₄
CAS Number:	20816-12-0
Molecular Weight:	254.23
MDL number:	MFCD00011150
PubChem Substance ID:	57652576
NACRES:	NA.47

Biochem/physiol Actions

Osmium tetroxide is also referred to as osmium and is mainly used as a secondary fixative of tissues. The molecule reacts with lipid moieties and is responsible for the oxidation of unsaturated bonds of fatty acids. This reaction adds density and contrast to biological samples. In normal tissues, presence of osmium results in intense black staining which can be viewed by normal eye. In addition, it can be used as a mordant (a molecule which combines with stain or dye at later stages) in electron microscopy, thereby enhancing lead staining.

5 mL in ampule
10 mL in ampule

Due to the hazardous nature of osmium tetroxide, it is recommended to use an ampule opener when using this chemical.

Quality Level	100,
reaction suitability	reagent type: oxidant
concentration	4% in H₂O
application(s)	electron microscopy: suitable, hematology: suitable, histology: suitable
color	colorless to yellow
pH	6.0-8.0
density	1.0 g/mL at 20 °C
storage temp.	2-8°C
SMILES string	O=[Os](=O)(=O)=O
InChI	1S/4O.Os
InChI key	VUVGYHUDAICLFK-UHFFFAOYSA-N

Used in synthetic applications of carbon-substituted iminium salts

Reactant for:

pictograms	GHS05,GHS06
signalword	Danger
hcodes	H302 + H332 - H310 - H315 - H318
pcodes	P262 - P280 - P301 + P312 - P302 + P352 + P310 - P304 + P340 + P312 - P305 + P351 + P338
Personal Protective Equipment	Faceshields,, Gloves,, Goggles,, type ABEK (EN14387) respirator filter,
RIDADR	UN 3287 6.1 / PGII
WGK Germany	WGK 1
Flash Point F	Not applicable
Flash Point C	Not applicable

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Oxalyl bromide

Empirical Formula (Hill Notation):	C₂Br₂O₂
Linear Formula:	BrCOCOBr
CAS Number:	15219-34-8
Molecular Weight:	215.83
Beilstein/REAXYS Number:	1744437
EC Number:	239-271-7
MDL number:	MFCD00000113
PubChem Substance ID:	24847129
NACRES:	NA.22

Synthesis of mutasynthons added to cultures of A. pretiosum for mutasynthetic generation of ansamitocin derivatives
Oxalic acid formation from hydroxyl radical substitutions
Cyclization to produce CRF1 receptor antagonists
Preparation, optical and electrochemical studies of thiophene end capped olig(2,3-alkylthieno[3,4-b]pyrazine)
Asymmetrical synthesis of glycosyl chlorides and bromides

Converts cyclopentane-1,3-dione to 3-bromocyclopenten-2-one.

25, 100 g in glass bottle

Quality Level	100,
assay	97%
reaction suitability	reagent type: oxidant
refractive index	n20/D 1.522 (lit.)
bp	16-17 °C/10 mmHg (lit.)
mp	19 °C (lit.)
storage temp.	2-8°C
SMILES string	BrC(=O)C(Br)=O
InChI	1S/C2Br2O2/c3-1(5)2(4)6
Inchi Key	JAZLVNXWYDFQFE-UHFFFAOYSA-N

Used in synthetic applications of carbon-substituted iminium salts

Reactant for:

pictograms	GHS05,GHS07
signalword	Danger
hcodes	H314 - H332
pcodes	P280 - P305 + P351 + P338 - P310
Supp Hazards	EUH014 - EUH029
Personal Protective Equipment	Faceshields,, Gloves,, Goggles,, type ABEK (EN14387) respirator filter,
RIDADR	UN 2922 6.1(8) / PGI
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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Oxalyl bromide solution

Empirical Formula (Hill Notation):	C₂Br₂O₂
Linear Formula:	BrCOCOBr
CAS Number:	15219-34-8
Molecular Weight:	215.83
MDL number:	MFCD00000113
PubChem Substance ID:	24859231

Synthesis of mutasynthons added to cultures of A. pretiosum for mutasynthetic generation of ansamitocin derivatives
Oxalic acid formation from hydroxyl radical substitutions
Cyclization to produce CRF1 receptor antagonists
Preparation, optical and electrochemical studies of thiophene end capped olig(2,3-alkylthieno[3,4-b]pyrazine)
Asymmetrical synthesis of glycosyl chlorides and bromides

50, 500 mL in Sure/Seal™

Quality Level	100,
reaction suitability	reagent type: oxidant
concentration	2.0 M in methylene chloride
density	1.517 g/mL at 25 °C
SMILES string	BrC(=O)C(Br)=O
InChI	1S/C2Br2O2/c3-1(5)2(4)6
Inchi Key	JAZLVNXWYDFQFE-UHFFFAOYSA-N

Oxalyl chloride is a commonly used chlorinating reagent that can be prepared by the reaction of oxalic acid and phosphorus pentachloride.

pictograms	GHS05,GHS07,GHS08
signalword	Danger
hcodes	H314 - H336 - H351
pcodes	P201 - P280 - P301 + P330 + P331 - P303 + P361 + P353 - P305 + P351 + P338 + P310 - P308 + P313
Target Organs	Central nervous system
Supp Hazards	EUH014 - EUH029
RIDADR	UN 2922 6.1(8) / PGII
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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Oxalyl chloride

Empirical Formula (Hill Notation):	C₂Cl₂O₂
Linear Formula:	ClCOCOCl
CAS Number:	79-37-8
Molecular Weight:	126.93
Beilstein/REAXYS Number:	1361988
EC Number:	201-200-2
MDL number:	MFCD00000704
PubChem Substance ID:	24853204
NACRES:	NA.22

Oxalyl chloride may be used in the following processes:

Preparation of Moshers acid chloride by reacting with Moshers acid in the presence of DMF.
Activation of dimethyl sulfoxide for use in the oxidation of long-chain alcohols to carbonyls.
Activation of -keto carboxylic acids and N-heterocyclic carboxylic acids for alkynylation to form ynediones and N-heterocyclic ynones, respectively.

Suitable for the synthesis of acid chlorides used to produce liquid crystals.
Reactant involved in:

Synthesis of N-heterocyclic ynones and ynediones, used to activate carboxylic acids
Chlorination and halogenation
Three-component [3+2] cycloadditions
Reactions with organostannanes
Synthesis of cyclopentenones
Carbonylations, used as a carbonyl synthon

5, 25, 100 g in ampule
10 kg in Nowpak™

ReagentPlus is a registered trademark of Sigma-Aldrich Co. LLC

vapor density	4.4 (vs air)
Quality Level	200,
vapor pressure	150 mmHg ( 20 °C)
product line	ReagentPlus^®
assay	99%
reaction suitability	reagent type: oxidant
impurities	<10 ppb Heavy metals
color	APHA: 0-150
refractive index	n20/D 1.429 (lit.)
bp	62-65 °C (lit.)
mp	10-8 °C (lit.)
density	1.5 g/mL at 20 °C (lit.)
SMILES string	ClC(=O)C(Cl)=O
InChI	1S/C2Cl2O2/c3-1(5)2(4)6
InChI key	CTSLXHKWHWQRSH-UHFFFAOYSA-N

Oxalyl chloride is generally used as a dimethyl sulfoxide activator and a chlorinating agent to convert carboxylic acid to acid chlorides.

pictograms	GHS02,GHS05,GHS06
signalword	Danger
hcodes	H225 - H260 - H314 - H331 - H335
pcodes	P210 - P231 + P232 - P280 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338
Target Organs	Respiratory system
Supp Hazards	EUH014 - EUH029
Personal Protective Equipment	Faceshields,, Gloves,, Goggles,
RIDADR	UN 2922 6.1(8) / PGI
WGK Germany	WGK 2
Flash Point F	51.8 °F - closed cup
Flash Point C	11.0 °C - closed cup

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Oxalyl chloride solution

Empirical Formula (Hill Notation):	C₂Cl₂O₂
Linear Formula:	ClCOCOCl
CAS Number:	79-37-8
Molecular Weight:	126.93
Beilstein/REAXYS Number:	1361988
MDL number:	MFCD00000704
PubChem Substance ID:	24858810
NACRES:	NA.22

100, 800 mL in Sure/Seal™

Quality Level	200,
reaction suitability	reagent type: oxidant
concentration	2.0 M in methylene chloride
density	1.335 g/mL at 25 °C
SMILES string	ClC(=O)C(Cl)=O
InChI	1S/C2Cl2O2/c3-1(5)2(4)6
InChI key	CTSLXHKWHWQRSH-UHFFFAOYSA-N

pictograms	GHS02,GHS05,GHS06,GHS08
signalword	Danger
hcodes	H260 - H302 - H314 - H331 - H336 - H351
pcodes	P231 + P232 - P280 - P301 + P312 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338
Target Organs	Central nervous system
Supp Hazards	EUH014 - EUH029 - EUH071
Personal Protective Equipment	Faceshields,, Gloves,, Goggles,, type ABEK (EN14387) respirator filter,
RIDADR	UN 2927 8(6.1) / PGII
WGK Germany	WGK 2
Flash Point F	Not applicable
Flash Point C	Not applicable

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OXONE® tetrabutylammonium salt

CAS Number:	104548-30-3
Beilstein/REAXYS Number:	5199887
PubChem Substance ID:	24886893
NACRES:	NA.22

Oxidation of Hantzsch 1,4-Dihydropyridines catalyzed by manganese(III) Schiff Base complexes
Epoxidation of alkenes
Oxidation of sulfides and olefins
Oxidation of alcohols
Oxidation of aromatic amines for synthesis of azoxy arenes

25, 100 g in poly bottle

Form of Oxone specially suited for the oxidation of sensitive compounds in CH2Cl2; Reagent for preparing 2-tetrahydrofuranyl ethers from alcohols and THF by radical coupling

OXONE is a registered trademark of E. I. du Pont de Nemours and Company

Quality Level	100,
grade	technical
assay	~1.6% active oxygen basis
reaction suitability	reagent type: oxidant
mp	144-146 °C
SMILES string	OS([O-])(=O)=O.[O-]S([O-])(=O)=O.OS(=O)(=O)O[O-].OS(=O)(=O)O[O-].CCCC[N+](CCCC)(CCCC)CCCC.CCCC[N+](CCCC)(CCCC)CCCC.CCCC[N+](CCCC)(CCCC)CCCC.CCCC[N+](CCCC)(CCCC)CCCC.CCCC[N+](CCCC)(CCCC)CCCC

OXONE®, monopersulfate compound is a potassium triple salt mainly used as a stable, easy to handle and nontoxic oxidant.

pictograms	GHS05,GHS07
signalword	Danger
hcodes	H302 - H314
pcodes	P260 - P280 - P301 + P312 + P330 - P301 + P330 + P331 - P303 + P361 + P353 - P305 + P351 + P338
Personal Protective Equipment	Eyeshields,, Faceshields,, Gloves,, type P1 (EN143) respirator filter,, type P3 (EN 143) respirator cartridges,
RIDADR	UN 3263 8 / PGIII
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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OXONE®, monopersulfate compound

Empirical Formula (Hill Notation):	HKO₅S · 0.5HKO₄S · 0.5K₂O₄S
Linear Formula:	KHSO₅ · 0.5KHSO₄ · 0.5K₂SO₄
CAS Number:	70693-62-8
Molecular Weight:	307.38
MDL number:	MFCD00040551
PubChem Substance ID:	57648006
NACRES:	NA.21

OXONE®, monopersulfate compound may be used as an alternative to transition-metal oxidants for the conversion of aldehydes to carboxylic acids or esters.
A rapid, efficient synthesis of oxaziridines from imines using buffered OXONE has been reported. Also used to study fading of an artists colorants.
Oxidant used for halogenation of a,b-unsaturated carbonyl compounds and catalytic generation of hypervalent iodine reagents for alcohol oxidation.
2-Iodoxybenzenesulfonic Acid as an Extremely Active Catalyst for the Selective Oxidation of Alcohols to Aldehydes, Ketones, Carboxylic Acids, and Enones with Oxone
A Convenient Halogenation of ,-Unsaturated Carbonyl Compounds with OXONE® and Hydrohalic Acid (HBr, HCl)
Oxidant used for halogenation of α,β-unsaturated carbonyl compounds and catalytic generation of hypervalent iodine reagents for alcohol oxidation.

100 g in poly bottle
5 g in glass bottle
5 kg in poly drum
1 kg in poly bottle
25 kg in fiber drum

OXONE is a registered trademark of E. I. du Pont de Nemours and Company

vapor pressure	<0.0000017 hPa
Quality Level	100
assay	>4.0% active oxygen basis (by Na₂S₂O₃, titration)
form	powder
reaction suitability	reagent type: oxidant
pH	2.1 (77 °C, 30 g/L)
SMILES string	[K+].[K+].[K+].[K+].[K+].OS([O-])(=O)=O.[O-]S([O-])(=O)=O.O[S+]([O-])([O-])(=O)=O.O[S+]([O-])([O-])(=O)=O
InChI	1S/5K.2H2O5S.2H2O4S/c;;;;;21-5-6(2,3)4;21-5(2,3)4/h;;;;;21H,(H,2,3,4);2(H2,1,2,3,4)/q5*+1;;;;/p-5
InChI key	HJKYXKSLRZKNSI-UHFFFAOYSA-I

Assay (HPLC, area%): 98.0 % (a/a)
Identity (IR): passes test

pictograms	GHS05,GHS07,GHS09
signalword	Danger
hcodes	H302 - H314 - H411
pcodes	P260 - P273 - P280 - P301 + P312 - P303 + P361 + P353 - P305 + P351 + P338
Personal Protective Equipment	Eyeshields, Faceshields, Gloves, type P1 (EN143) respirator filter, type P3 (EN 143) respirator cartridges
RIDADR	UN 3260 8 / PGII
WGK Germany	WGK 2
Flash Point F	does not flash
Flash Point C	does not flash

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p-Chloranil

Empirical Formula (Hill Notation):	C₆Cl₄O₂
CAS Number:	118-75-2
Molecular Weight:	245.88
MDL number:	MFCD00001594
EC Index Number:	204-274-4

Assay (ICP-OES): ≥ 99.0 %

storage conditions	Store below +30°C.
vapor pressure	1 hPa ( 71 °C)
Quality Level	200,
assay	98.0% (HPLC)
autoignition temp.	>400 °C
potency	4000 mg/kg LD₅₀, oral (Rat)
reaction suitability	reagent type: oxidant
pH	3.5-4.5 (20 °C, 100 g/L in H₂O, slurry)
mp	290-293 °C (sublimed)
solubility	practically insoluble 0.25 g/L
bulk density	800 kg/m³
storage temp.	2-30°C
InChI	1S/C6Cl4O2/c7-1-2(8)6(12)4(10)3(9)5(1)11
Inchi Key	UGNWTBMOAKPKBL-UHFFFAOYSA-N

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Palladium(II) acetate (47% Pd)

Empirical Formula (Hill Notation):	C₄H₆O₄Pd
Linear Formula:	(CH₃COO)₂Pd
CAS Number:	3375-31-3
Molecular Weight:	224.51
MDL number:	MFCD00012453
EC Index Number:	222-164-4

Кат. номер
8180569999
8180568500
8180560005
8180560001
8.18056.0005
8.18056.8500
8.18056.0001

Analysis Note

Peracetic acid solution may be used as a reaction media to transform phenyldimethylsilyl group to hydroxyl group attached to carbon.

storage conditions	Store below +30°C.
Quality Level	200,
potency	5110 mg/kg LD₅₀, oral (Rat)
reaction suitability	reagent type: oxidant
pH	2-3 (20 °C in H₂O, aqueous suspension)
mp	205 °C
storage temp.	2-30°C
InChI	1S/2C2H4O2.Pd/c21-2(3)4;/h21H3,(H,3,4);/q;;+2/p-2
Inchi Key	YJVFFLUZDVXJQI-UHFFFAOYSA-L

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Peracetic acid solution

Empirical Formula (Hill Notation):	C₂H₄O₃
Linear Formula:	CH₃CO₃H
CAS Number:	79-21-0
Molecular Weight:	76.05
Beilstein/REAXYS Number:	1098464
MDL number:	MFCD00002128
PubChem Substance ID:	329756332
NACRES:	NA.21

Quality Level	200,
assay	36-40% (by Na₂S₂O₃, redox titration)
form	liquid
reaction suitability	reagent type: oxidant
availability	available only in EU
concentration	36-40 wt. % in acetic acid
density	1.13 g/cm³
storage temp.	2-8°C
SMILES string	CC(=O)OO
InChI	1S/C2H4O3/c1-2(3)5-4/h4H,1H3
Inchi Key	KFSLWBXXFJQRDL-UHFFFAOYSA-N

Perchloric acid can be used as:

pictograms	GHS02,GHS05,GHS07,GHS09
signalword	Danger
hcodes	H226 - H242 - H302 + H312 + H332 - H314 - H335 - H410
pcodes	P210 - P273 - P280 - P303 + P361 + P353 - P305 + P351 + P338 - P370 + P378
Target Organs	Respiratory system
WGK Germany	WGK 2
Flash Point F	132.8 °F - closed cup
Flash Point C	56 °C - closed cup

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Perchloric acid

Empirical Formula (Hill Notation):	HClO₄
Linear Formula:	HClO₄
CAS Number:	7601-90-3
Molecular Weight:	100.46
MDL number:	MFCD00011325
PubChem Substance ID:	24858523
NACRES:	NA.22

A reaction medium in oxidation reactions.
A reagent for the preparation of fluorinated polymer electrolytes using poly (vinylidenefluoride-cohexafluoropropylene) (PVDF-HFP) for fuel cell applications.
A dopant in the preparation of perchloric acid-functionalized polyaniline (HClO4/PANI) catalyst for the synthesis of 2-substituted benzothiazoles by condensation reaction between o-aminothiophenol with aldehydes.

Perchloric acid (HClO4) can be used in the preparation of:

Silica supported perchloric acid (HClO4-SiO2) which is used as a catalyst in geminal diacylation of aldehydes, synthesis of amidoalkyl naphthols, primary carbamates, and tetrasubstituted imidazoles.
Alumina supported perchloric acid (Al2O3-HClO4), which is used as a catalyst in the synthesis of -(-amidobenzyl)--naphthols.
Fe3O4@SiO2-HClO4 catalyst, which is used in the synthesis of 1,4-dihydropyridine derivatives.

1 L in glass bottle
50, 250 mL in glass bottle

Quality Level	100,
vapor pressure	6.8 mmHg ( 25 °C)
assay	70%, 99.999% trace metals basis
form	liquid
reaction suitability	reagent type: oxidant
density	1.664 g/mL at 25 °C
SMILES string	OCl(=O)(=O)=O
InChI	1S/ClHO4/c2-1(3,4)5/h(H,2,3,4,5)
InChI key	VLTRZXGMWDSKGL-UHFFFAOYSA-N

pictograms	GHS03,GHS05,GHS07,GHS08
signalword	Danger
hcodes	H271 - H290 - H302 - H314 - H373
pcodes	P210 - P280 - P301 + P312 - P303 + P361 + P353 - P305 + P351 + P338 - P314
Target Organs	Thyroid
Personal Protective Equipment	Faceshields,, Gloves,, Goggles,, type ABEK (EN14387) respirator filter,
RIDADR	UN 1873 8(5.1) / PGI
WGK Germany	WGK 1

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Perchloric acid-d solution

Empirical Formula (Hill Notation):	ClDO₄
Linear Formula:	DClO₄ / D₂O
CAS Number:	19029-50-6
Molecular Weight:	101.46
MDL number:	MFCD00044234
PubChem Substance ID:	24850597
NACRES:	NA.12

Quality Level	200,
isotopic purity	99 atom % D
reaction suitability	reagent type: oxidant
concentration	68 wt. % in D₂O
application(s)	NMR: suitable
refractive index	n20/D 1.4165
density	1.680 g/mL at 25 °C
mass shift	M+1
SMILES string	[2H]OCl(=O)(=O)=O
InChI	1S/ClHO4/c2-1(3,4)5/h(H,2,3,4,5)/i/hD
InChI key	VLTRZXGMWDSKGL-DYCDLGHISA-N

25, 100, 500 g in glass bottle

pictograms	GHS03,GHS05
signalword	Danger
hcodes	H271 - H314
pcodes	P210 - P280 - P301 + P330 + P331 - P303 + P361 + P353 - P305 + P351 + P338 + P310
RIDADR	UN 1873 8(5.1) / PGI
WGK Germany	WGK 3
Flash Point F	235.4 °F - closed cup
Flash Point C	113 °C - closed cup

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Periodic acid

Empirical Formula (Hill Notation):	H₅IO₆
CAS Number:	10450-60-9
Molecular Weight:	227.94
EC Number:	233-937-0
MDL number:	MFCD00011344
PubChem Substance ID:	329820319

ReagentPlus is a registered trademark of Sigma-Aldrich Co. LLC

product line	ReagentPlus^®
Quality Level	100,
assay	99.0%
form	powder or crystals
reaction suitability	reagent type: oxidant
application(s)	toxicology assay: suitable
mp	122 °C (lit.)
solubility	water: 100 mg/mL, clear, colorless
SMILES string	OI(O)(O)(O)(O)=O
InChI	1S/H5IO6/c2-1(3,4,5,6)7/h(H5,2,3,4,5,6,7)
Inchi Key	TWLXDPFBEPBAQB-UHFFFAOYSA-N

For use in procedure no. 395 for Periodic Acid-Schiff (PAS) and Silver Stain Procedure No. HT100.

pictograms	GHS03,GHS05,GHS08,GHS09
signalword	Danger
hcodes	H271 - H314 - H372 - H410
pcodes	P210 - P260 - P273 - P280 - P303 + P361 + P353 - P305 + P351 + P338
Target Organs	Thyroid
RIDADR	UN 3085 8(5.1) / PGII
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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Periodic acid solution

MDL number:	MFCD00011344
PubChem Substance ID:	24864646

Quality Level	500,
clinical	for in vitro diagnostic use
shelf life	expiry date on label
reaction suitability	reagent type: oxidant
IVD	for in vitro diagnostic use
concentration	1 g/dL in deionized water
shipped in	wet ice
storage temp.	2-8°C
SMILES string	OI(O)(O)(O)(O)=O
InChI	1S/H5IO6/c2-1(3,4,5,6)7/h(H5,2,3,4,5,6,7)
Inchi Key	TWLXDPFBEPBAQB-UHFFFAOYSA-N

Method: Colorimetric, with test strips, 0.5 - 2 - 5 - 10 - 25 mg/L (H2O2), MQuant®
Peroxide is an all purpose disinfectant which, due to its excellent antiviral, bactericidal and fungicidal action, is widely used in the food industry. Here, the MQuant® test strips are ideal for controlling the residual peroxide after disinfection. Peroxidase transfers peroxide oxygen to an organic redox indicator. This produces a blue oxidation product. The peroxide concentration is measured semiquantitatively by visual comparison of the reaction zone of the test strip with the fields of a color scale. The test strips are perfect for pre-testing a sample in an economic and quick way to estimate the peroxide concentration and a possible dilution factor prior to using a quantitative method such as a Reflectoquant® or Spectroquant® Peroxide test.

pictograms	GHS05,GHS08
signalword	Danger
hcodes	H314 - H373 - H412
pcodes	P260 - P273 - P280 - P303 + P361 + P353 - P305 + P351 + P338 - P314
Target Organs	Thyroid
Personal Protective Equipment	Faceshields,, Gloves,, Goggles,, type ABEK (EN14387) respirator filter,
RIDADR	UN 3264 8 / PGII
WGK Germany	WGK 2
Flash Point F	Not applicable
Flash Point C	Not applicable

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Peroxide Test

Linkage

Replaces: 10011-1; 10011

MQUANT is a registered trademark of Merck KGaA, Darmstadt, Germany
REFLECTOQUANT is a registered trademark of Merck KGaA, Darmstadt, Germany
SPECTROQUANT is a registered trademark of Merck KGaA, Darmstadt, Germany

storage conditions	Store at +2°C to +8°C.
Quality Level	100,
description	semi-quantitative
product line	MQuant^®
specific analyte(s)	hydrogen peroxide
reaction suitability	reaction type: enzymatic reaction, reagent type: oxidant
measuring range	0.5-25 mg/L (H₂O₂)
detection method	colorimetric
storage temp.	2-8°C

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Phenol nitroprusside solution

120 mL in glass bottle

Suitable for the colorimetric determination of ammonia using alkaline hypochlorite (A1727) solution as used in urea nitrogen assays

Contains sodium nitroprusside, phenol and EDTA.

reaction suitability	reagent type: oxidant
Quality Level	200,
storage temp.	2-8°C

pictograms	GHS05,GHS07,GHS08
signalword	Danger
hcodes	H302 - H314 - H341 - H412
pcodes	P273 - P280 - P301 + P312 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338
RIDADR	UN 2821 6.1 / PGIII
WGK Germany	WGK 2
Flash Point F	Not applicable
Flash Point C	Not applicable

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Phenyl[3-(trifluoromethyl)phenyl]iodonium triflate

Empirical Formula (Hill Notation):	C₁₄H₉F₆IO₃S
CAS Number:	905718-46-9
Molecular Weight:	498.18
Beilstein/REAXYS Number:	10503310
MDL number:	MFCD21608481
PubChem Substance ID:	329765638
NACRES:	NA.22

Quality Level	100,
assay	≥98% (HPLC)
composition	carbon, 32.9-34.6% CH
reaction suitability	reagent type: oxidant
SMILES string	[O-]S(=O)(=O)C(F)(F)F.FC(F)(F)c1cccc([I+]c2ccccc2)c1
InChI	1S/C13H9F3I.CHF3O3S/c14-13(15,16)10-5-4-8-12(9-10)17-11-6-2-1-3-7-11;2-1(3,4)8(5,6)7/h1-9H;(H,5,6,7)/q+1;/p-1
InChI key	OSSLDNUSYGVAIB-UHFFFAOYSA-M