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1,5-Naphthalene diisocyanate

CAS No.
3173-72-6
Chemical Name:
1,5-Naphthalene diisocyanate
Synonyms
ndi;1,5-DIISOCYANATONAPHTHALENE;1,5-NAPHTHYLENE DIISOCYANATE;Naphthylene-1,5-diisocyanate;1,5-NDI;desmodur15;40KGS/DRUM;1,5-naphthalene;1,5-Naphthalene diis;NAPHTHYLENEDIISOCYANATE
CBNumber:
CB1715235
Molecular Formula:
C12H6N2O2
Molecular Weight:
210.19
MDL Number:
MFCD00039588
MOL File:
3173-72-6.mol
Last updated:2024-03-28 16:55:20

1,5-Naphthalene diisocyanate Properties

Melting point 130°C
Boiling point 244°C (100 torr)
Density 1.45
vapor pressure 0.001Pa at 25℃
refractive index 1.6000 (estimate)
storage temp. Inert atmosphere,2-8°C
solubility Chloroform (Slightly), DMSO (Slightly)
form powder to lump
color White to Light yellow
Water Solubility soluable
Stability Hygroscopic
InChIKey SBJCUZQNHOLYMD-UHFFFAOYSA-N
LogP 0.91 at 25℃
CAS DataBase Reference 3173-72-6(CAS DataBase Reference)
EWG's Food Scores 5
FDA UNII 0ORB22ST7M
IARC 3 (Vol. 19, Sup 7, 71) 1999
NIST Chemistry Reference Naphthalene, 1,5-diisocyanato-(3173-72-6)
EPA Substance Registry System 1,5-Naphthalene diisocyanate (3173-72-6)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictogramsGHS hazard pictograms
GHS06,GHS07,GHS08
Signal word  Danger
Hazard statements  H315-H319-H330-H334-H335-H412
Precautionary statements  P260-P264-P271-P273-P280-P284-P302+P352+P332+P313+P362+P364-P304+P340+P310-P305+P351+P338+P337+P313-P403+P233-P405-P501
Hazard Codes  Xn
Risk Statements  20-36/37/38-42-52/53-37-26-36/38
Safety Statements  26-28-38-45-61-42-36-51-22
RIDADR  2206
RTECS  NQ9600000
HazardClass  6.1(b)
PackingGroup  III
HS Code  29291090
NFPA 704
1
3 0

1,5-Naphthalene diisocyanate price More Price(10)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TCI Chemical N0168 1,5-Diisocyanatonaphthalene >98.0%(GC) 3173-72-6 25g $149 2024-03-01 Buy
TCI Chemical N0168 1,5-Diisocyanatonaphthalene >98.0%(GC) 3173-72-6 100g $365 2024-03-01 Buy
TRC D679083 1,5-Diisocyanatonaphthalene 3173-72-6 250mg $50 2021-12-16 Buy
AK Scientific H176 1,5-Naphthylenediisocyanate 3173-72-6 25g $103 2021-12-16 Buy
Frontier Specialty Chemicals JK326787 1,5-Diisocyanatonaphthalene 98% 3173-72-6 25g $119 2021-12-16 Buy
Product number Packaging Price Buy
N0168 25g $149 Buy
N0168 100g $365 Buy
D679083 250mg $50 Buy
H176 25g $103 Buy
JK326787 25g $119 Buy

1,5-Naphthalene diisocyanate Chemical Properties,Uses,Production

Description

Naphthalene diisocyanate (NDI) occurs as white to lightyellow crystalline flakes with a characteristic odor. NDI is incompatible with many classes of compounds, reacting exothermically to release toxic gases. Reactions with amines, aldehydes, alcohols, alkali metals, ketones, mercaptans, strong oxidizers, hydrides, phenols, and peroxides can cause vigorous releases of heat. Acids and bases initiate polymerization reactions. NDI can react with water to form amines and liberate carbon dioxide.

Chemical Properties

Naphthylene 1,5-diisocyanate is a solid, m.p. 128°C. It has a lower vapour pressure than tolylene diisocyanate and is therefore less toxic in use; it does, however, have sensitizing properties.

Uses

Naphthylene 1,5-diisocyanate is mainly used for the production of elastomers.

Uses

NDI is used as a curing agent in the manufacture of elastomers.

Uses

Manufacture of polyurethane solid elastomers.

Definition

ChEBI: 1,5-Naphthalene diisocyanate is a member of naphthalenes.

Preparation

Naphthylene 1,5-diisocyanate (NDI) is prepared from naphthalene as follows:

3173-72-6 synthesis

General Description

White to light-yellow crystalline flakes.

Reactivity Profile

Isocyanates and thioisocyanates, such as 1,5-Naphthalene diisocyanate, are incompatible with many classes of compounds, reacting exothermically to release toxic gases. Reactions with amines, aldehydes, alcohols, alkali metals, ketones, mercaptans, strong oxidizers, hydrides, phenols, and peroxides can cause vigorous releases of heat. Acids and bases initiate polymerization reactions in these materials. Some isocyanates react with water to form amines and liberate carbon dioxide. Base-catalysed reactions of isocyanates with alcohols should be carried out in inert solvents. Such reactions in the absence of solvents often occur with explosive violence, [Wischmeyer(1969)].

Hazard

Irritant. Questionable carcinogen.

Flammability and Explosibility

Non flammable

Safety Profile

A powerful allergen. An irritant. Questionable carcinogen. When heated to decomposition it emits toxic fumes of NOx.

Environmental Fate

NDI is a synthetic organic chemical. It is a natural derivative of primary amines with the general formula R–N]C]O which does not occur naturally in the environment. At room temperature it can be a liquid or crystal. It is miscible with alcohol, diglycol, monoethyl ether, ether, acetone, carbon tetrachloride, benzene, chlorobenzene, kerosene, and olive oil; however, it may react violently with alcohol, water, acid, bases, and strong alkaline materials and tertiary amines and generate enough heat to self-ignite and release toxic combustion products. NDI is not readily biodegradable; however, it reacts with water and most acids producing unstable carbonic acids, which subsequently decarboxylate yielding relatively chemically inert and insoluble polymeric urea. While these polyureas are persistent, studies have indicated that they pose virtually no potential for adverse impacts on the aquatic environment. Due to hydrolysis in water, bioaccumulation of NDI is not expected. Since the hydrolysis products formed are irritants, there is a potential for inhalation exposure. The degree stability is a function of humidity.

Toxicity evaluation

The toxicological properties of isocyanates are attributed to the –N=C=O group. It is thought to react vigorously and exothermically with water forming an unstable carbamic acid that dissociates to form a primary amine with liberation of CO2. Hence, the primary amine will react further generating a urea derivative. Isocyanates also react readily with all organic compounds resulting in polymerization. Such reactions denature proteins, form abnormal crosslinkages, and generally disorganize the protein resulting in alteration of its normal function. This reactivity with proteins can account for its potency as a sensitizing agent. An IgE- or IgG-mediated mechanism has been proposed, but has not been definitively linked to isocyanate exposure. There is also evidence that inflammation and morphological changes of the bronchia mucosa and direct neurogenic mechanisms could be involved in the mechanics of toxicity. Thus, more than one reaction may occur in a system at a given time.

124244-58-2
3173-72-6
Synthesis of 1,5-Naphthalene diisocyanate from Carbamic acid, 1,5-naphthalenediylbis-, dibutyl ester (9CI)

1,5-Naphthalene diisocyanate Preparation Products And Raw materials

Global( 291)Suppliers
Supplier Tel Email Country ProdList Advantage
Dayang Chem (Hangzhou) Co.,Ltd.
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naphthylene-1,5-diisocyanate pictures 2024-03-29 naphthylene-1,5-diisocyanate
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US $0.00 / KG 1KG 99% 50000KG/month Hebei Mojin Biotechnology Co., Ltd
1,5-Naphthalene diisocyanate pictures 2023-09-06 1,5-Naphthalene diisocyanate
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US $0.00-0.00 / KG 1KG 99% 500000kg Hebei Guanlang Biotechnology Co., Ltd.
1,5-NAPHTHALENEDIISOCYANATE NAPHTHALENE 1,5-DIISOCYANATE 1,5-diisocyanato-naphthalen Naphthyl 1,5-diisocyanate ISOCYANICACID,1,5-NAPHTHALENEESTER NAPHTHYLENEDIISOCYANATE NAPHTHALENE,5-DIISOCYANATO-1- 1,5-naphalene diisocyanate(NDI) 1,5-NAPHALENE DIISOCYANATE 1,5-Di-Isocyanate-Naphthatene (NDI) (Naphthalene-1,5-diyl) bisisocyanate (Naphthalene-1,5-diyl) diisocyanate 1,5-Naphthalenediyl diisocyanate 1,5-Naphthalene diis 1,5-naphthalene diisocyanate(NDI) 1,5-diisocyanatonaph-thalate 5-Naphthylene diisocyanate 1,5-NAPHTHALENEDIISOCYANATE (NDI)99% 1,5-naphthalene 1,5-naphthyldiisocyanate desmodur15 Isocyanic acid, 1,5-naphthylene ester isocyanicacid,1,5-naphthyleneester naphthalene,1,5,-diisocyanato- naphthalene,1,5-diisocyanato- 1,5-Naphthalenediisocyanate -Carc. 1,5-NDI 40KGS/DRUM 1,5-Diisocyanatonaphthalene> 1,5-Naphthalene diisocyanate ISO 9001:2015 REACH 1,5-NAPHTHYLENE DIISOCYANATE 1,5-DIISOCYANATONAPHTHALENE Naphthylene-1,5-diisocyanate ndi 3173-72-6 C10H6NCO2 C12H6N2O2